A concise synthesis of (R)-hydroxy-E,Z-diene fatty acids: preparation of 12(R)-hete, tetranor-12(R)-hete, and 13(R)-hode

Sun Lumin; J R Falck; Michal L. Schwartzman

doi:10.1016/S0040-4039(00)79912-6

A concise synthesis of (R)-hydroxy-E,Z-diene fatty acids: preparation of 12(R)-hete, tetranor-12(R)-hete, and 13(R)-hode

Sun Lumin, J R Falck, Michal L. Schwartzman

Biochemistry

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

13 Scopus citations

Abstract

Chiral E-enals derived from functionalized 2-deoxy-D-ribofuranoses by ylide-induced β-elimination were exploited for the synthesis of fatty acid metabolites containing the (R)-hydroxy-E,Z-diene subunit.

Original language	English (US)
Pages (from-to)	2315-2318
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	21
DOIs	https://doi.org/10.1016/S0040-4039(00)79912-6
State	Published - May 20 1991

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)79912-6

Cite this

@article{3b9a5e616cd7407b85e661a47203f91f,

title = "A concise synthesis of (R)-hydroxy-E,Z-diene fatty acids: preparation of 12(R)-hete, tetranor-12(R)-hete, and 13(R)-hode",

abstract = "Chiral E-enals derived from functionalized 2-deoxy-D-ribofuranoses by ylide-induced β-elimination were exploited for the synthesis of fatty acid metabolites containing the (R)-hydroxy-E,Z-diene subunit.",

author = "Sun Lumin and Falck, {J R} and Schwartzman, {Michal L.}",

year = "1991",

month = may,

day = "20",

doi = "10.1016/S0040-4039(00)79912-6",

language = "English (US)",

volume = "32",

pages = "2315--2318",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "21",

}

TY - JOUR

T1 - A concise synthesis of (R)-hydroxy-E,Z-diene fatty acids

T2 - preparation of 12(R)-hete, tetranor-12(R)-hete, and 13(R)-hode

AU - Lumin, Sun

AU - Falck, J R

AU - Schwartzman, Michal L.

PY - 1991/5/20

Y1 - 1991/5/20

N2 - Chiral E-enals derived from functionalized 2-deoxy-D-ribofuranoses by ylide-induced β-elimination were exploited for the synthesis of fatty acid metabolites containing the (R)-hydroxy-E,Z-diene subunit.

AB - Chiral E-enals derived from functionalized 2-deoxy-D-ribofuranoses by ylide-induced β-elimination were exploited for the synthesis of fatty acid metabolites containing the (R)-hydroxy-E,Z-diene subunit.

UR - http://www.scopus.com/inward/record.url?scp=0025819106&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025819106&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)79912-6

DO - 10.1016/S0040-4039(00)79912-6

M3 - Article

AN - SCOPUS:0025819106

SN - 0040-4039

VL - 32

SP - 2315

EP - 2318

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 21

ER -

A concise synthesis of (R)-hydroxy-E,Z-diene fatty acids: preparation of 12(R)-hete, tetranor-12(R)-hete, and 13(R)-hode

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this