Stereocontrolled Construction of Complex Cyclic Ketones via Oxy‐Cope Rearrangement
- 1 June 1990
- journal article
- review article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 29 (6), 609-626
- https://doi.org/10.1002/anie.199006091
Abstract
No abstract availableKeywords
This publication has 118 references indexed in Scilit:
- A formal total synthesis of (.+-.)-9-isocyanopupukeananeThe Journal of Organic Chemistry, 1989
- Synthesis of a Tricyclic Steroid Intermediate Via an Oxy-Cope RearrangementSynthetic Communications, 1989
- Studies on the Synthesis of Eremophilane Sesquiterpenes. A Novel Entry into the Aristolane Ring SystemSynthetic Communications, 1986
- Macroexpansion methodology. 3. Eight-step synthesis of (-)-(3Z)-cembrene AJournal of the American Chemical Society, 1985
- Total synthesis of (.+-.)-poitediol and (.+-.)4-epipoitediolJournal of the American Chemical Society, 1984
- Practical method for .alpha.-alkenyl ketone synthesis based on a facile reductive rearrangement of alkynyl halohydrinsJournal of the American Chemical Society, 1983
- Preparation and rearrangement of 1,2-dialkenylcyclobutanols. A useful method for synthesis of substituted cyclooctenonesThe Journal of Organic Chemistry, 1982
- .alpha. Vinylation of ketones. A general method using (phenylseleno)acetaldehydeThe Journal of Organic Chemistry, 1982
- Ring expansion of 3-methoxy-6-vinyl-7,8,9,10-tetrahydro-6(5H)-benzocyclooctenolThe Journal of Organic Chemistry, 1980
- An expeditious route to the germacranes. Total synthesis of (.+-.)-acoragermacrone and (.+-.)-preisocalamendiolJournal of the American Chemical Society, 1977