Enantiospecific synthesis of methyl 11,12- and 14,15-epoxyeicosatrienoate

J R Falck; Sukumar Manna; Jorge Capdevila

doi:10.1016/S0040-4039(01)81200-4

Enantiospecific synthesis of methyl 11,12- and 14,15-epoxyeicosatrienoate

J R Falck, Sukumar Manna, Jorge Capdevila

Biochemistry

Research output: Contribution to journal › Article › peer-review

24 Scopus citations

Abstract

The methyl esters of the cytochrome P-450 epoxygenase metabolites 11(S),12(R)-and 14(R),15(S)-epoxyeicosatrienoic acid and some analogues were prepared enantiospecifically from 15(S)-HETE derived precursors.

Original language	English (US)
Pages (from-to)	2443-2446
Number of pages	4
Journal	Tetrahedron Letters
Volume	25
Issue number	23
DOIs	https://doi.org/10.1016/S0040-4039(01)81200-4
State	Published - 1984

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)81200-4

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@article{8e07c6eed1924f7c9b3eb23843d9ff6d,

title = "Enantiospecific synthesis of methyl 11,12- and 14,15-epoxyeicosatrienoate",

abstract = "The methyl esters of the cytochrome P-450 epoxygenase metabolites 11(S),12(R)-and 14(R),15(S)-epoxyeicosatrienoic acid and some analogues were prepared enantiospecifically from 15(S)-HETE derived precursors.",

author = "Falck, {J R} and Sukumar Manna and Jorge Capdevila",

year = "1984",

doi = "10.1016/S0040-4039(01)81200-4",

language = "English (US)",

volume = "25",

pages = "2443--2446",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "23",

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TY - JOUR

T1 - Enantiospecific synthesis of methyl 11,12- and 14,15-epoxyeicosatrienoate

AU - Falck, J R

AU - Manna, Sukumar

AU - Capdevila, Jorge

PY - 1984

Y1 - 1984

N2 - The methyl esters of the cytochrome P-450 epoxygenase metabolites 11(S),12(R)-and 14(R),15(S)-epoxyeicosatrienoic acid and some analogues were prepared enantiospecifically from 15(S)-HETE derived precursors.

AB - The methyl esters of the cytochrome P-450 epoxygenase metabolites 11(S),12(R)-and 14(R),15(S)-epoxyeicosatrienoic acid and some analogues were prepared enantiospecifically from 15(S)-HETE derived precursors.

UR - http://www.scopus.com/inward/record.url?scp=0004914668&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0004914668&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(01)81200-4

DO - 10.1016/S0040-4039(01)81200-4

M3 - Article

AN - SCOPUS:0004914668

SN - 0040-4039

VL - 25

SP - 2443

EP - 2446

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 23

ER -

Enantiospecific synthesis of methyl 11,12- and 14,15-epoxyeicosatrienoate

Abstract

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