Asymmetric synthesis of chiral spirocyclanes: Selective formation of 2-acyloxy-1-oxospiro[4.n]alkanes by regio- and stereoselective rearrangement of α,β-epoxy acylates in bicyclo[n.3.0]alkane systems-Reference-Cited by-同舟云学术

Asymmetric synthesis of chiral spirocyclanes: Selective formation of 2-acyloxy-1-oxospiro[4.n]alkanes by regio- and stereoselective rearrangement of α,β-epoxy acylates in bicyclo[n.3.0]alkane systems

Published:1995-05 Issue:18 Volume:36 Page:3219-3222
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujioka Hiromichi,Kitagaki Shinji,Imai Reiko,Kondo Michinori,Okamoto Sachi,Yoshida Yutaka,Akai Shuji,Kita Yasuyuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

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2. Spectroscopic properties of two nonenolizable α-keto-γ-lactones, dehydroginkgolide A and 3,3-dimethyl-2-oxo-γ-butyrolactone

3. Synthesis of spiro[4.5]decane ring system through allylsilane promoted spiroannulation

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