Acyclic stereoselection. 21. Synthesis of an ionophore synthon having four asymmetric carbons by sequential aldol addition, claisen rearrangement and hydroboration-Reference-Cited by-同舟云学术

Acyclic stereoselection. 21. Synthesis of an ionophore synthon having four asymmetric carbons by sequential aldol addition, claisen rearrangement and hydroboration

Published:1984-01 Issue:3 Volume:25 Page:243-246
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Heathcock Clayton H.,Jarvi Esa T.,Rosen Terry

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference6 articles.

1. For part 20, see S.-I. Kiyooka and C.H. Heathcock, Tetrahedron Lett., in press.

2. Acyclic stereoselection. 15. Sequential aldol-claisen as a method for 1,5-stereoselection. Total synthesis of the vitamin-E side chain

3. 1,4-Stereoselection by sequential aldol addition–Claisen rearrangement. Stereostructure of the C30diol from Messel shale kerogen

4. Acyclic stereoselection—13

5. Experiments Directed toward the Total Synthesis of Terpenes. VI. The Stereochemistry of Isopimaric Acid1,2

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