vic-Diol chirons

Enantiospecific synthesis of 11,12- and 14,15-dihydroxyeicosatrienoic acids

Kamlesh Chauhan, Sivasubramanian Aravind, Sang Gyeong Lee, J R Falck, Jorge H. Capdevila

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

A differentiated, six-carbon vicinal-diol chiron was prepared from D-glucurono-6,3-lactone and exploited in the asymmetric synthesis of the erythro/threo-isomers of the title eicosanoids.

Original languageEnglish (US)
Pages (from-to)6791-6794
Number of pages4
JournalTetrahedron Letters
Volume35
Issue number37
DOIs
StatePublished - Sep 12 1994

Fingerprint

Eicosanoids
Lactones
Isomers
Carbon
chiron
14,15-dihydroxyeicosatrienoic acid
11,12-dihydroxyeicosatrienoic acid

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

vic-Diol chirons : Enantiospecific synthesis of 11,12- and 14,15-dihydroxyeicosatrienoic acids. / Chauhan, Kamlesh; Aravind, Sivasubramanian; Lee, Sang Gyeong; Falck, J R; Capdevila, Jorge H.

In: Tetrahedron Letters, Vol. 35, No. 37, 12.09.1994, p. 6791-6794.

Research output: Contribution to journalArticle

Chauhan, Kamlesh ; Aravind, Sivasubramanian ; Lee, Sang Gyeong ; Falck, J R ; Capdevila, Jorge H. / vic-Diol chirons : Enantiospecific synthesis of 11,12- and 14,15-dihydroxyeicosatrienoic acids. In: Tetrahedron Letters. 1994 ; Vol. 35, No. 37. pp. 6791-6794.
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