Volume 18, Issue 38
Natural Products
Full Access

ChemInform Abstract: Total Synthesis of 5(S),20- and 15(S),20-Dihydroxyeicosatetraenoic Acid and 5(S),6(R)-Epoxy-20-hydroxy- and 14(R),15(S)-Epoxy-20-hydroxyeicosatrienoic Acid.

S. LUMIN

S. LUMIN

Dep. Mol. Genet. Biochem., Univ. Texas Health Sci. Center, Dallas, TX 75235, USA

Search for more papers by this author
P. YADAGIRI

P. YADAGIRI

Dep. Mol. Genet. Biochem., Univ. Texas Health Sci. Center, Dallas, TX 75235, USA

Search for more papers by this author
J. R. FALCK

J. R. FALCK

Dep. Mol. Genet. Biochem., Univ. Texas Health Sci. Center, Dallas, TX 75235, USA

Search for more papers by this author
J. CAPDEVILA

J. CAPDEVILA

Dep. Mol. Genet. Biochem., Univ. Texas Health Sci. Center, Dallas, TX 75235, USA

Search for more papers by this author
P. MOSSET

P. MOSSET

Dep. Mol. Genet. Biochem., Univ. Texas Health Sci. Center, Dallas, TX 75235, USA

Search for more papers by this author
R. GREE

R. GREE

Dep. Mol. Genet. Biochem., Univ. Texas Health Sci. Center, Dallas, TX 75235, USA

Search for more papers by this author
First published: September 22, 1987

Abstract

The aldehyde (II) is transformed into the epoxy aldehyde (IV) which undergoes a Wittig reaction with the phosphorane (V).

ChemInform Abstract

The aldehyde (II) is transformed into the epoxy aldehyde (IV) which undergoes a Wittig reaction with the phosphorane (V). Subsequent desilylation and hydrolysis yield the acid (VI). The acids (VII) - (IX) are also prepared from (II) in a similar manner.

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.