Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites.
The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well....
Ausführliche Beschreibung
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| Autor*in: |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1990 |
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| Reproduktion: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
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| Übergeordnetes Werk: |
in: Tetrahedron Letters - Amsterdam : Elsevier, 31(1990), 7, Seite 1003-1006 |
| Übergeordnetes Werk: |
volume:31 ; year:1990 ; number:7 ; pages:1003-1006 |
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| 245 | 1 | 0 | |a Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. |
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| 520 | |a The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. | ||
| 520 | |a The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. | ||
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| 700 | 1 | |a Depezay, J.C. |4 oth | |
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(DE-627)NLEJ176261923 (DE-599)GBVNLZ176261923 DE-627 ger DE-627 rakwb eng Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Le Merrer, Y. oth Gravier-Pelletier, C. oth Dumas, J. oth Depezay, J.C. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 7, Seite 1003-1006 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:7 pages:1003-1006 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)94414-9 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 7 1003-1006 |
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(DE-627)NLEJ176261923 (DE-599)GBVNLZ176261923 DE-627 ger DE-627 rakwb eng Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Le Merrer, Y. oth Gravier-Pelletier, C. oth Dumas, J. oth Depezay, J.C. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 7, Seite 1003-1006 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:7 pages:1003-1006 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)94414-9 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 7 1003-1006 |
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(DE-627)NLEJ176261923 (DE-599)GBVNLZ176261923 DE-627 ger DE-627 rakwb eng Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Le Merrer, Y. oth Gravier-Pelletier, C. oth Dumas, J. oth Depezay, J.C. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 7, Seite 1003-1006 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:7 pages:1003-1006 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)94414-9 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 7 1003-1006 |
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(DE-627)NLEJ176261923 (DE-599)GBVNLZ176261923 DE-627 ger DE-627 rakwb eng Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Le Merrer, Y. oth Gravier-Pelletier, C. oth Dumas, J. oth Depezay, J.C. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 7, Seite 1003-1006 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:7 pages:1003-1006 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)94414-9 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 7 1003-1006 |
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(DE-627)NLEJ176261923 (DE-599)GBVNLZ176261923 DE-627 ger DE-627 rakwb eng Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Le Merrer, Y. oth Gravier-Pelletier, C. oth Dumas, J. oth Depezay, J.C. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 7, Seite 1003-1006 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:7 pages:1003-1006 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)94414-9 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 7 1003-1006 |
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Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites |
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Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. |
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chiral α-hydroxy- and α,β-dihydroxy- aldehydes from d-isoascorbic and l-ascorbic acids. useful precursors for the synthesis of fatty acid metabolites |
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Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. |
| abstract |
The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. |
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The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. |
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The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well. |
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Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ176261923</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210706020724.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070505s1990 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ176261923</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)GBVNLZ176261923</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">Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites.</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1990</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">The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">The four possible stereoisomers of α,β-dihydroxyaldehydes, useful building blocks for the synthesis of fatty acid metabolites, are synthesized via epoxy-tetrolis derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral α-hydroxyaldehydes as well.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Elsevier Journal Backfiles on ScienceDirect 1907 - 2002</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Le Merrer, Y.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gravier-Pelletier, C.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dumas, J.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Depezay, J.C.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Tetrahedron Letters</subfield><subfield code="d">Amsterdam : Elsevier</subfield><subfield code="g">31(1990), 7, Seite 1003-1006</subfield><subfield code="w">(DE-627)NLEJ175981779</subfield><subfield code="w">(DE-600)2007074-3</subfield><subfield code="x">0040-4039</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:31</subfield><subfield code="g">year:1990</subfield><subfield code="g">number:7</subfield><subfield code="g">pages:1003-1006</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)94414-9</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_H</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-SDJ</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">31</subfield><subfield code="j">1990</subfield><subfield code="e">7</subfield><subfield code="h">1003-1006</subfield></datafield></record></collection>
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7.40189 |