Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol
Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the form...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
1997 |
|---|
| Umfang: |
4 |
|---|
| Reproduktion: |
Springer Online Journal Archives 1860-2002 |
|---|---|
| Übergeordnetes Werk: |
in: Applied microbiology and biotechnology - 1975, 48(1997) vom: März, Seite 363-366 |
| Übergeordnetes Werk: |
volume:48 ; year:1997 ; month:03 ; pages:363-366 ; extent:4 |
| Links: |
|---|
| Katalog-ID: |
NLEJ202756556 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | NLEJ202756556 | ||
| 003 | DE-627 | ||
| 005 | 20230506144357.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 070528s1997 xx |||||o 00| ||eng c | ||
| 035 | |a (DE-627)NLEJ202756556 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 245 | 1 | 0 | |a Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| 264 | 1 | |c 1997 | |
| 300 | |a 4 | ||
| 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 Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. | ||
| 533 | |f Springer Online Journal Archives 1860-2002 | ||
| 700 | 1 | |a Bianchi, D. |4 oth | |
| 700 | 1 | |a Bernardi, A. |4 oth | |
| 700 | 1 | |a Bosetti, A. |4 oth | |
| 700 | 1 | |a Bortolo, R. |4 oth | |
| 700 | 1 | |a Cidaria, D. |4 oth | |
| 700 | 1 | |a Crespi, E. |4 oth | |
| 700 | 1 | |a Gagliardi, I. |4 oth | |
| 773 | 0 | 8 | |i in |t Applied microbiology and biotechnology |d 1975 |g 48(1997) vom: März, Seite 363-366 |w (DE-627)NLEJ188988920 |w (DE-600)1464336-4 |x 1432-0614 |7 nnns |
| 773 | 1 | 8 | |g volume:48 |g year:1997 |g month:03 |g pages:363-366 |g extent:4 |
| 856 | 4 | 0 | |u http://dx.doi.org/10.1007/s002530051063 |
| 912 | |a GBV_USEFLAG_U | ||
| 912 | |a ZDB-1-SOJ | ||
| 912 | |a GBV_NL_ARTICLE | ||
| 951 | |a AR | ||
| 952 | |d 48 |j 1997 |c 3 |h 363-366 |g 4 | ||
| matchkey_str |
article:14320614:1997----::yteiodhdoyahhlnioesyirbaoia |
|---|---|
| hierarchy_sort_str |
1997 |
| publishDate |
1997 |
| allfields |
(DE-627)NLEJ202756556 DE-627 ger DE-627 rakwb eng Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol 1997 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. Springer Online Journal Archives 1860-2002 Bianchi, D. oth Bernardi, A. oth Bosetti, A. oth Bortolo, R. oth Cidaria, D. oth Crespi, E. oth Gagliardi, I. oth in Applied microbiology and biotechnology 1975 48(1997) vom: März, Seite 363-366 (DE-627)NLEJ188988920 (DE-600)1464336-4 1432-0614 nnns volume:48 year:1997 month:03 pages:363-366 extent:4 http://dx.doi.org/10.1007/s002530051063 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 48 1997 3 363-366 4 |
| spelling |
(DE-627)NLEJ202756556 DE-627 ger DE-627 rakwb eng Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol 1997 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. Springer Online Journal Archives 1860-2002 Bianchi, D. oth Bernardi, A. oth Bosetti, A. oth Bortolo, R. oth Cidaria, D. oth Crespi, E. oth Gagliardi, I. oth in Applied microbiology and biotechnology 1975 48(1997) vom: März, Seite 363-366 (DE-627)NLEJ188988920 (DE-600)1464336-4 1432-0614 nnns volume:48 year:1997 month:03 pages:363-366 extent:4 http://dx.doi.org/10.1007/s002530051063 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 48 1997 3 363-366 4 |
| allfields_unstemmed |
(DE-627)NLEJ202756556 DE-627 ger DE-627 rakwb eng Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol 1997 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. Springer Online Journal Archives 1860-2002 Bianchi, D. oth Bernardi, A. oth Bosetti, A. oth Bortolo, R. oth Cidaria, D. oth Crespi, E. oth Gagliardi, I. oth in Applied microbiology and biotechnology 1975 48(1997) vom: März, Seite 363-366 (DE-627)NLEJ188988920 (DE-600)1464336-4 1432-0614 nnns volume:48 year:1997 month:03 pages:363-366 extent:4 http://dx.doi.org/10.1007/s002530051063 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 48 1997 3 363-366 4 |
| allfieldsGer |
(DE-627)NLEJ202756556 DE-627 ger DE-627 rakwb eng Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol 1997 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. Springer Online Journal Archives 1860-2002 Bianchi, D. oth Bernardi, A. oth Bosetti, A. oth Bortolo, R. oth Cidaria, D. oth Crespi, E. oth Gagliardi, I. oth in Applied microbiology and biotechnology 1975 48(1997) vom: März, Seite 363-366 (DE-627)NLEJ188988920 (DE-600)1464336-4 1432-0614 nnns volume:48 year:1997 month:03 pages:363-366 extent:4 http://dx.doi.org/10.1007/s002530051063 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 48 1997 3 363-366 4 |
| allfieldsSound |
(DE-627)NLEJ202756556 DE-627 ger DE-627 rakwb eng Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol 1997 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. Springer Online Journal Archives 1860-2002 Bianchi, D. oth Bernardi, A. oth Bosetti, A. oth Bortolo, R. oth Cidaria, D. oth Crespi, E. oth Gagliardi, I. oth in Applied microbiology and biotechnology 1975 48(1997) vom: März, Seite 363-366 (DE-627)NLEJ188988920 (DE-600)1464336-4 1432-0614 nnns volume:48 year:1997 month:03 pages:363-366 extent:4 http://dx.doi.org/10.1007/s002530051063 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 48 1997 3 363-366 4 |
| language |
English |
| source |
in Applied microbiology and biotechnology 48(1997) vom: März, Seite 363-366 volume:48 year:1997 month:03 pages:363-366 extent:4 |
| sourceStr |
in Applied microbiology and biotechnology 48(1997) vom: März, Seite 363-366 volume:48 year:1997 month:03 pages:363-366 extent:4 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| isfreeaccess_bool |
false |
| container_title |
Applied microbiology and biotechnology |
| authorswithroles_txt_mv |
Bianchi, D. @@oth@@ Bernardi, A. @@oth@@ Bosetti, A. @@oth@@ Bortolo, R. @@oth@@ Cidaria, D. @@oth@@ Crespi, E. @@oth@@ Gagliardi, I. @@oth@@ |
| publishDateDaySort_date |
1997-03-01T00:00:00Z |
| hierarchy_top_id |
NLEJ188988920 |
| id |
NLEJ202756556 |
| 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">NLEJ202756556</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230506144357.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070528s1997 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ202756556</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="245" ind1="1" ind2="0"><subfield code="a">Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1997</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">4</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">Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Springer Online Journal Archives 1860-2002</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bianchi, D.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bernardi, A.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bosetti, A.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bortolo, R.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Cidaria, D.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Crespi, E.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gagliardi, I.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Applied microbiology and biotechnology</subfield><subfield code="d">1975</subfield><subfield code="g">48(1997) vom: März, Seite 363-366</subfield><subfield code="w">(DE-627)NLEJ188988920</subfield><subfield code="w">(DE-600)1464336-4</subfield><subfield code="x">1432-0614</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:48</subfield><subfield code="g">year:1997</subfield><subfield code="g">month:03</subfield><subfield code="g">pages:363-366</subfield><subfield code="g">extent:4</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1007/s002530051063</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-SOJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">48</subfield><subfield code="j">1997</subfield><subfield code="c">3</subfield><subfield code="h">363-366</subfield><subfield code="g">4</subfield></datafield></record></collection>
|
| series2 |
Springer Online Journal Archives 1860-2002 |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)NLEJ188988920 |
| format |
electronic Article |
| delete_txt_mv |
keep |
| collection |
NL |
| remote_str |
true |
| illustrated |
Not Illustrated |
| issn |
1432-0614 |
| topic_title |
Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
zu |
| author2_variant |
d b db a b ab a b ab r b rb d c dc e c ec i g ig |
| hierarchy_parent_title |
Applied microbiology and biotechnology |
| hierarchy_parent_id |
NLEJ188988920 |
| hierarchy_top_title |
Applied microbiology and biotechnology |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)NLEJ188988920 (DE-600)1464336-4 |
| title |
Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| spellingShingle |
Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| ctrlnum |
(DE-627)NLEJ202756556 |
| title_full |
Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| journal |
Applied microbiology and biotechnology |
| journalStr |
Applied microbiology and biotechnology |
| lang_code |
eng |
| isOA_bool |
false |
| recordtype |
marc |
| publishDateSort |
1997 |
| contenttype_str_mv |
zzz |
| container_start_page |
363 |
| container_volume |
48 |
| physical |
4 |
| format_se |
Elektronische Aufsätze |
| title_sort |
synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| title_auth |
Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| abstract |
Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. |
| abstractGer |
Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. |
| abstract_unstemmed |
Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols. |
| collection_details |
GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE |
| title_short |
Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol |
| url |
http://dx.doi.org/10.1007/s002530051063 |
| remote_bool |
true |
| author2 |
Bianchi, D. Bernardi, A. Bosetti, A. Bortolo, R. Cidaria, D. Crespi, E. Gagliardi, I. |
| author2Str |
Bianchi, D. Bernardi, A. Bosetti, A. Bortolo, R. Cidaria, D. Crespi, E. Gagliardi, I. |
| ppnlink |
NLEJ188988920 |
| mediatype_str_mv |
z |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| author2_role |
oth oth oth oth oth oth oth |
| up_date |
2024-07-06T08:47:13.674Z |
| _version_ |
1803818771337445376 |
| 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">NLEJ202756556</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230506144357.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070528s1997 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ202756556</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="245" ind1="1" ind2="0"><subfield code="a">Synthesis of dihydroxynaphthalene isomers by microbial oxidation of 1- and 2-naphthol</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1997</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">4</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">Abstract The mutant strain Pseudomonas fluorescens TTC1 (NCIMB 40605), derived from the naphthalene-degrading Pseudomonas fluorescens N3 (NCIMB 40530), was used for the oxidation of 1- and 2-naphthols to give different isomers of dihydroxynaphthalene. The oxidation reactions proceed through the formation of dihydrodiol intermediates, which are too unstable to be isolated, since they spontaneously eliminate water to give the fully aromatic dihydroxynaphthalenes. The high regioselectivity of the dehydration reaction was confirmed by the study of the acid-catalysed aromatization of a series of stable monosubstituted naphthalene cis-1,2-dihydrodiols.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Springer Online Journal Archives 1860-2002</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bianchi, D.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bernardi, A.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bosetti, A.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bortolo, R.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Cidaria, D.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Crespi, E.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gagliardi, I.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Applied microbiology and biotechnology</subfield><subfield code="d">1975</subfield><subfield code="g">48(1997) vom: März, Seite 363-366</subfield><subfield code="w">(DE-627)NLEJ188988920</subfield><subfield code="w">(DE-600)1464336-4</subfield><subfield code="x">1432-0614</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:48</subfield><subfield code="g">year:1997</subfield><subfield code="g">month:03</subfield><subfield code="g">pages:363-366</subfield><subfield code="g">extent:4</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1007/s002530051063</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-SOJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">48</subfield><subfield code="j">1997</subfield><subfield code="c">3</subfield><subfield code="h">363-366</subfield><subfield code="g">4</subfield></datafield></record></collection>
|
| score |
7.4007196 |