Ring differentiation of the trans-decahydronaphthalene system via chemo-enzymatic dissymmetrization of its σ-symmetric glycol: Synthesis of a highly functionalized chiral building block for the terpene synthesis-Reference-Cited by-同舟云学术

Ring differentiation of the trans-decahydronaphthalene system via chemo-enzymatic dissymmetrization of its σ-symmetric glycol: Synthesis of a highly functionalized chiral building block for the terpene synthesis

Published:1993-07 Issue:28 Volume:34 Page:4539-4540
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Toyooka Naoki,Nishino Akira,Momose Takefumi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. Asymmetric twin-ring differentiation by lipase-catalyzed enantiotoposelective reaction of the ring-crossed meso glycol: Asymmetric synthesis of a highly functionalized piperidine from the conjoined twin piperidine system

2. Studies on reductive alkylation: Synthesis of Wieland-Miescher ketone analogues bearing an oxygenated angular substituent

3. Isolation and Structure of Maingayic Acid, a Piscicidal

4. Structure of ajugarins

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