Synthesis of a cis-5-cyclodecenone and cis fused hydronaphthalenols through control of the stereochemistry of the oxy-Cope rearrangement with the tri-n-propylsilyl substituent-Reference-Cited by-同舟云学术

Synthesis of a cis-5-cyclodecenone and cis fused hydronaphthalenols through control of the stereochemistry of the oxy-Cope rearrangement with the tri-n-propylsilyl substituent

Published:1997-10 Issue:42 Volume:53 Page:14235-14246
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chu Yongliang,Colclough David,Hotchkin David,Tuazon Myla,White James B.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Preparation of bicyclo[5.3.0]decan-1-ols from the tandem anionic oxy-Cope rearrangement/allylsilane cyclization of 1,2-divinylcyclohexanols

2. Synthesis of either a cis- or trans-fused hydroazulenol from an allylstannane functionalized (E)-5-cyclodecenone

3. Total synthesis of (.+-.)-africanol and (.+-.)-isoafricanol

4. Electrophilic and radical transannular cyclizations of 5-cyclodecenone to give either hydronaphthalene or hydroazulene products

5. A FACILE ROUTE TO MACROCYCLIC KETONES. DIRECT DIVINYLATION OF 2-CHLOROCYCLODODECAN-1-ONE

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1. Synthesis of 5-cyclodecenones via RCM and a three-pot sequence for bisannulation;Tetrahedron Letters;2016-09

2. Removable Silyl Group as a “Masked Proton” in Oxy-2-oxonia(azonia)-Cope Rearrangement: Applications in Stereoselective Total Synthesis of Natural Macrolides;European Journal of Organic Chemistry;2015-07-01

3. 3.06 Transannular Electrophilic Cyclizations;Comprehensive Organic Synthesis II;2014

4. Geminal acylation of α-heterosubstituted cyclohexanones and their ketals;Canadian Journal of Chemistry;2010-11

5. ChemInform Abstract: Synthesis of a cis-5-Cyclodecenone and cis-Fused Hydronaphthalenols Through Control of the Stereochemistry of the Oxy-Cope Rearrangement with the Tri-n-propylsilyl Substituent.;ChemInform;2010-06-24