Stereocontrolled synthesis of (±)-methyl 3,6-epoxy-4,6,8-triethyl-2,4,9-dodecatrienoate, a major metabolite of Caribbean sponge, Plakortis halichondrioides, using reactions of alkylidenecarbenes in one pot-Reference-Cited by-同舟云学术

Stereocontrolled synthesis of (±)-methyl 3,6-epoxy-4,6,8-triethyl-2,4,9-dodecatrienoate, a major metabolite of Caribbean sponge, Plakortis halichondrioides, using reactions of alkylidenecarbenes in one pot

Published:2005-10 Issue:44 Volume:46 Page:7483-7485
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Akiyama Megumi,Isoda Yuichi,Nishimoto Masato,Kobayashi Aki,Togawa Daisuke,Hirao Nobuaki,Kuboki Atsuhito,Ohira Susumu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Metabolites of three marine sponges of the genus Plakortis

2. Plakortides M and N, Bioactive Polyketide Endoperoxides from the Caribbean Marine Sponge Plakortis halichondrioides

3. Absolute configuration of methyl (2Z,6R,8R,9E)-3,6-epoxy-4,6,8-triethyl-2,4,9-dodecatrienoate from the sponge Plakortis halichondrioides

4. Synthesis in the Plakortone Series: Plakortone E

5. Metabolites from the sponge plakortis simplex. II.

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