Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction
• Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enanti...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Goncalves, Fernanda Jorge [verfasserIn] |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2018 |
|---|
| Schlagwörter: |
|---|
| Umfang: |
7 |
|---|
| Übergeordnetes Werk: |
Enthalten in: Residue co-evolution helps predict interaction sites in α-helical membrane proteins - Zeng, Bo ELSEVIER, 2019, an international journal devoted to scientific and technological aspects of industrially important polysaccharides, Amsterdam [u.a.] |
|---|---|
| Übergeordnetes Werk: |
volume:181 ; year:2018 ; day:1 ; month:02 ; pages:1206-1212 ; extent:7 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.carbpol.2017.12.012 |
|---|
| Katalog-ID: |
ELV041421418 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | ELV041421418 | ||
| 003 | DE-627 | ||
| 005 | 20230624084925.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 180726s2018 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1016/j.carbpol.2017.12.012 |2 doi | |
| 028 | 5 | 2 | |a /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica |
| 035 | |a (DE-627)ELV041421418 | ||
| 035 | |a (ELSEVIER)S0144-8617(17)31409-1 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 082 | 0 | 4 | |a 540 |q VZ |
| 084 | |a BIODIV |q DE-30 |2 fid | ||
| 084 | |a 42.13 |2 bkl | ||
| 100 | 1 | |a Goncalves, Fernanda Jorge |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction |
| 264 | 1 | |c 2018 | |
| 300 | |a 7 | ||
| 336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
| 337 | |a nicht spezifiziert |b z |2 rdamedia | ||
| 338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
| 520 | |a • Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. | ||
| 650 | 7 | |a Heterogeneous catalysis |2 Elsevier | |
| 650 | 7 | |a Modified chitosan |2 Elsevier | |
| 650 | 7 | |a Solid-state 13C NMR |2 Elsevier | |
| 650 | 7 | |a Copper |2 Elsevier | |
| 650 | 7 | |a Henry reaction |2 Elsevier | |
| 700 | 1 | |a Kamal, Fadwa |4 oth | |
| 700 | 1 | |a Gaucher, Anne |4 oth | |
| 700 | 1 | |a Gil, Richard |4 oth | |
| 700 | 1 | |a Bourdreux, Flavien |4 oth | |
| 700 | 1 | |a Martineau-Corcos, Charlotte |4 oth | |
| 700 | 1 | |a Gurgel, Leandro Vinícius Alves |4 oth | |
| 700 | 1 | |a Gil, Laurent Frédéric |4 oth | |
| 700 | 1 | |a Prim, Damien |4 oth | |
| 773 | 0 | 8 | |i Enthalten in |n Elsevier Science |a Zeng, Bo ELSEVIER |t Residue co-evolution helps predict interaction sites in α-helical membrane proteins |d 2019 |d an international journal devoted to scientific and technological aspects of industrially important polysaccharides |g Amsterdam [u.a.] |w (DE-627)ELV002183382 |
| 773 | 1 | 8 | |g volume:181 |g year:2018 |g day:1 |g month:02 |g pages:1206-1212 |g extent:7 |
| 856 | 4 | 0 | |u https://doi.org/10.1016/j.carbpol.2017.12.012 |3 Volltext |
| 912 | |a GBV_USEFLAG_U | ||
| 912 | |a GBV_ELV | ||
| 912 | |a SYSFLAG_U | ||
| 912 | |a FID-BIODIV | ||
| 912 | |a SSG-OLC-PHA | ||
| 936 | b | k | |a 42.13 |j Molekularbiologie |q VZ |
| 951 | |a AR | ||
| 952 | |d 181 |j 2018 |b 1 |c 0201 |h 1206-1212 |g 7 | ||
| author_variant |
f j g fj fjg |
|---|---|
| matchkey_str |
goncalvesfernandajorgekamalfadwagauchera:2018----:yteicaatrstoadplctooprdnmdfecioadrvtvsoteisnn |
| hierarchy_sort_str |
2018 |
| bklnumber |
42.13 |
| publishDate |
2018 |
| allfields |
10.1016/j.carbpol.2017.12.012 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica (DE-627)ELV041421418 (ELSEVIER)S0144-8617(17)31409-1 DE-627 ger DE-627 rakwb eng 540 VZ BIODIV DE-30 fid 42.13 bkl Goncalves, Fernanda Jorge verfasserin aut Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction 2018 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier • Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction Elsevier Kamal, Fadwa oth Gaucher, Anne oth Gil, Richard oth Bourdreux, Flavien oth Martineau-Corcos, Charlotte oth Gurgel, Leandro Vinícius Alves oth Gil, Laurent Frédéric oth Prim, Damien oth Enthalten in Elsevier Science Zeng, Bo ELSEVIER Residue co-evolution helps predict interaction sites in α-helical membrane proteins 2019 an international journal devoted to scientific and technological aspects of industrially important polysaccharides Amsterdam [u.a.] (DE-627)ELV002183382 volume:181 year:2018 day:1 month:02 pages:1206-1212 extent:7 https://doi.org/10.1016/j.carbpol.2017.12.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.13 Molekularbiologie VZ AR 181 2018 1 0201 1206-1212 7 |
| spelling |
10.1016/j.carbpol.2017.12.012 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica (DE-627)ELV041421418 (ELSEVIER)S0144-8617(17)31409-1 DE-627 ger DE-627 rakwb eng 540 VZ BIODIV DE-30 fid 42.13 bkl Goncalves, Fernanda Jorge verfasserin aut Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction 2018 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier • Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction Elsevier Kamal, Fadwa oth Gaucher, Anne oth Gil, Richard oth Bourdreux, Flavien oth Martineau-Corcos, Charlotte oth Gurgel, Leandro Vinícius Alves oth Gil, Laurent Frédéric oth Prim, Damien oth Enthalten in Elsevier Science Zeng, Bo ELSEVIER Residue co-evolution helps predict interaction sites in α-helical membrane proteins 2019 an international journal devoted to scientific and technological aspects of industrially important polysaccharides Amsterdam [u.a.] (DE-627)ELV002183382 volume:181 year:2018 day:1 month:02 pages:1206-1212 extent:7 https://doi.org/10.1016/j.carbpol.2017.12.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.13 Molekularbiologie VZ AR 181 2018 1 0201 1206-1212 7 |
| allfields_unstemmed |
10.1016/j.carbpol.2017.12.012 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica (DE-627)ELV041421418 (ELSEVIER)S0144-8617(17)31409-1 DE-627 ger DE-627 rakwb eng 540 VZ BIODIV DE-30 fid 42.13 bkl Goncalves, Fernanda Jorge verfasserin aut Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction 2018 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier • Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction Elsevier Kamal, Fadwa oth Gaucher, Anne oth Gil, Richard oth Bourdreux, Flavien oth Martineau-Corcos, Charlotte oth Gurgel, Leandro Vinícius Alves oth Gil, Laurent Frédéric oth Prim, Damien oth Enthalten in Elsevier Science Zeng, Bo ELSEVIER Residue co-evolution helps predict interaction sites in α-helical membrane proteins 2019 an international journal devoted to scientific and technological aspects of industrially important polysaccharides Amsterdam [u.a.] (DE-627)ELV002183382 volume:181 year:2018 day:1 month:02 pages:1206-1212 extent:7 https://doi.org/10.1016/j.carbpol.2017.12.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.13 Molekularbiologie VZ AR 181 2018 1 0201 1206-1212 7 |
| allfieldsGer |
10.1016/j.carbpol.2017.12.012 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica (DE-627)ELV041421418 (ELSEVIER)S0144-8617(17)31409-1 DE-627 ger DE-627 rakwb eng 540 VZ BIODIV DE-30 fid 42.13 bkl Goncalves, Fernanda Jorge verfasserin aut Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction 2018 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier • Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction Elsevier Kamal, Fadwa oth Gaucher, Anne oth Gil, Richard oth Bourdreux, Flavien oth Martineau-Corcos, Charlotte oth Gurgel, Leandro Vinícius Alves oth Gil, Laurent Frédéric oth Prim, Damien oth Enthalten in Elsevier Science Zeng, Bo ELSEVIER Residue co-evolution helps predict interaction sites in α-helical membrane proteins 2019 an international journal devoted to scientific and technological aspects of industrially important polysaccharides Amsterdam [u.a.] (DE-627)ELV002183382 volume:181 year:2018 day:1 month:02 pages:1206-1212 extent:7 https://doi.org/10.1016/j.carbpol.2017.12.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.13 Molekularbiologie VZ AR 181 2018 1 0201 1206-1212 7 |
| allfieldsSound |
10.1016/j.carbpol.2017.12.012 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica (DE-627)ELV041421418 (ELSEVIER)S0144-8617(17)31409-1 DE-627 ger DE-627 rakwb eng 540 VZ BIODIV DE-30 fid 42.13 bkl Goncalves, Fernanda Jorge verfasserin aut Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction 2018 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier • Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction Elsevier Kamal, Fadwa oth Gaucher, Anne oth Gil, Richard oth Bourdreux, Flavien oth Martineau-Corcos, Charlotte oth Gurgel, Leandro Vinícius Alves oth Gil, Laurent Frédéric oth Prim, Damien oth Enthalten in Elsevier Science Zeng, Bo ELSEVIER Residue co-evolution helps predict interaction sites in α-helical membrane proteins 2019 an international journal devoted to scientific and technological aspects of industrially important polysaccharides Amsterdam [u.a.] (DE-627)ELV002183382 volume:181 year:2018 day:1 month:02 pages:1206-1212 extent:7 https://doi.org/10.1016/j.carbpol.2017.12.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.13 Molekularbiologie VZ AR 181 2018 1 0201 1206-1212 7 |
| language |
English |
| source |
Enthalten in Residue co-evolution helps predict interaction sites in α-helical membrane proteins Amsterdam [u.a.] volume:181 year:2018 day:1 month:02 pages:1206-1212 extent:7 |
| sourceStr |
Enthalten in Residue co-evolution helps predict interaction sites in α-helical membrane proteins Amsterdam [u.a.] volume:181 year:2018 day:1 month:02 pages:1206-1212 extent:7 |
| format_phy_str_mv |
Article |
| bklname |
Molekularbiologie |
| institution |
findex.gbv.de |
| topic_facet |
Heterogeneous catalysis Modified chitosan Solid-state 13C NMR Copper Henry reaction |
| dewey-raw |
540 |
| isfreeaccess_bool |
false |
| container_title |
Residue co-evolution helps predict interaction sites in α-helical membrane proteins |
| authorswithroles_txt_mv |
Goncalves, Fernanda Jorge @@aut@@ Kamal, Fadwa @@oth@@ Gaucher, Anne @@oth@@ Gil, Richard @@oth@@ Bourdreux, Flavien @@oth@@ Martineau-Corcos, Charlotte @@oth@@ Gurgel, Leandro Vinícius Alves @@oth@@ Gil, Laurent Frédéric @@oth@@ Prim, Damien @@oth@@ |
| publishDateDaySort_date |
2018-01-01T00:00:00Z |
| hierarchy_top_id |
ELV002183382 |
| dewey-sort |
3540 |
| id |
ELV041421418 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV041421418</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230624084925.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180726s2018 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.carbpol.2017.12.012</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">/cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV041421418</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0144-8617(17)31409-1</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">BIODIV</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">42.13</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Goncalves, Fernanda Jorge</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2018</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">7</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">• Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Heterogeneous catalysis</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Modified chitosan</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Solid-state 13C NMR</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Copper</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Henry reaction</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kamal, Fadwa</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gaucher, Anne</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gil, Richard</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bourdreux, Flavien</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Martineau-Corcos, Charlotte</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gurgel, Leandro Vinícius Alves</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gil, Laurent Frédéric</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Prim, Damien</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="a">Zeng, Bo ELSEVIER</subfield><subfield code="t">Residue co-evolution helps predict interaction sites in α-helical membrane proteins</subfield><subfield code="d">2019</subfield><subfield code="d">an international journal devoted to scientific and technological aspects of industrially important polysaccharides</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV002183382</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:181</subfield><subfield code="g">year:2018</subfield><subfield code="g">day:1</subfield><subfield code="g">month:02</subfield><subfield code="g">pages:1206-1212</subfield><subfield code="g">extent:7</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.carbpol.2017.12.012</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-BIODIV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">42.13</subfield><subfield code="j">Molekularbiologie</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">181</subfield><subfield code="j">2018</subfield><subfield code="b">1</subfield><subfield code="c">0201</subfield><subfield code="h">1206-1212</subfield><subfield code="g">7</subfield></datafield></record></collection>
|
| author |
Goncalves, Fernanda Jorge |
| spellingShingle |
Goncalves, Fernanda Jorge ddc 540 fid BIODIV bkl 42.13 Elsevier Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction |
| authorStr |
Goncalves, Fernanda Jorge |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)ELV002183382 |
| format |
electronic Article |
| dewey-ones |
540 - Chemistry & allied sciences |
| delete_txt_mv |
keep |
| author_role |
aut |
| collection |
elsevier |
| remote_str |
true |
| illustrated |
Not Illustrated |
| topic_title |
540 VZ BIODIV DE-30 fid 42.13 bkl Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction Elsevier |
| topic |
ddc 540 fid BIODIV bkl 42.13 Elsevier Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction |
| topic_unstemmed |
ddc 540 fid BIODIV bkl 42.13 Elsevier Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction |
| topic_browse |
ddc 540 fid BIODIV bkl 42.13 Elsevier Heterogeneous catalysis Elsevier Modified chitosan Elsevier Solid-state 13C NMR Elsevier Copper Elsevier Henry reaction |
| format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
zu |
| author2_variant |
f k fk a g ag r g rg f b fb c m c cmc l v a g lva lvag l f g lf lfg d p dp |
| hierarchy_parent_title |
Residue co-evolution helps predict interaction sites in α-helical membrane proteins |
| hierarchy_parent_id |
ELV002183382 |
| dewey-tens |
540 - Chemistry |
| hierarchy_top_title |
Residue co-evolution helps predict interaction sites in α-helical membrane proteins |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)ELV002183382 |
| title |
Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction |
| ctrlnum |
(DE-627)ELV041421418 (ELSEVIER)S0144-8617(17)31409-1 |
| title_full |
Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction |
| author_sort |
Goncalves, Fernanda Jorge |
| journal |
Residue co-evolution helps predict interaction sites in α-helical membrane proteins |
| journalStr |
Residue co-evolution helps predict interaction sites in α-helical membrane proteins |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
500 - Science |
| recordtype |
marc |
| publishDateSort |
2018 |
| contenttype_str_mv |
zzz |
| container_start_page |
1206 |
| author_browse |
Goncalves, Fernanda Jorge |
| container_volume |
181 |
| physical |
7 |
| class |
540 VZ BIODIV DE-30 fid 42.13 bkl |
| format_se |
Elektronische Aufsätze |
| author-letter |
Goncalves, Fernanda Jorge |
| doi_str_mv |
10.1016/j.carbpol.2017.12.012 |
| dewey-full |
540 |
| title_sort |
synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic cu-catalysed henry reaction |
| title_auth |
Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction |
| abstract |
• Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. |
| abstractGer |
• Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. |
| abstract_unstemmed |
• Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%. |
| collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA |
| title_short |
Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction |
| url |
https://doi.org/10.1016/j.carbpol.2017.12.012 |
| remote_bool |
true |
| author2 |
Kamal, Fadwa Gaucher, Anne Gil, Richard Bourdreux, Flavien Martineau-Corcos, Charlotte Gurgel, Leandro Vinícius Alves Gil, Laurent Frédéric Prim, Damien |
| author2Str |
Kamal, Fadwa Gaucher, Anne Gil, Richard Bourdreux, Flavien Martineau-Corcos, Charlotte Gurgel, Leandro Vinícius Alves Gil, Laurent Frédéric Prim, Damien |
| ppnlink |
ELV002183382 |
| mediatype_str_mv |
z |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| author2_role |
oth oth oth oth oth oth oth oth |
| doi_str |
10.1016/j.carbpol.2017.12.012 |
| up_date |
2024-07-06T20:04:35.733Z |
| _version_ |
1803861387625103360 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV041421418</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230624084925.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180726s2018 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.carbpol.2017.12.012</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">/cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001061.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV041421418</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0144-8617(17)31409-1</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">BIODIV</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">42.13</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Goncalves, Fernanda Jorge</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis, characterisation and application of pyridine-modified chitosan derivatives for the first non-racemic Cu-catalysed Henry reaction</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2018</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">7</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">• Pyridine-modified chitosan derivatives were applied in nitroaldol (Henry) reaction. • Solid-state 13C MC-CP MAS was applied to elucidate the catalyst structures. • 47(±2)% of chitosan-free NH2 groups were grafted for both C1 and C2 catalysts. • C1-Cu(OAc)2 provided a high conversion and the enantiomeric excess increased to 19(±4)%. • C2-Cu(OAc)2 provided a higher conversion, but the enantiomeric excess was 14.5(±1.5)%.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Heterogeneous catalysis</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Modified chitosan</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Solid-state 13C NMR</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Copper</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Henry reaction</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kamal, Fadwa</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gaucher, Anne</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gil, Richard</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bourdreux, Flavien</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Martineau-Corcos, Charlotte</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gurgel, Leandro Vinícius Alves</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gil, Laurent Frédéric</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Prim, Damien</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="a">Zeng, Bo ELSEVIER</subfield><subfield code="t">Residue co-evolution helps predict interaction sites in α-helical membrane proteins</subfield><subfield code="d">2019</subfield><subfield code="d">an international journal devoted to scientific and technological aspects of industrially important polysaccharides</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV002183382</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:181</subfield><subfield code="g">year:2018</subfield><subfield code="g">day:1</subfield><subfield code="g">month:02</subfield><subfield code="g">pages:1206-1212</subfield><subfield code="g">extent:7</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.carbpol.2017.12.012</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-BIODIV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">42.13</subfield><subfield code="j">Molekularbiologie</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">181</subfield><subfield code="j">2018</subfield><subfield code="b">1</subfield><subfield code="c">0201</subfield><subfield code="h">1206-1212</subfield><subfield code="g">7</subfield></datafield></record></collection>
|
| score |
7.3986187 |