Research & Teaching Faculty

STEREOSELECTIVITY OF C(3) METHYLATION AND ALDOL CONDENSATION OF CAMPHOR AND DERIVATIVES

TitleSTEREOSELECTIVITY OF C(3) METHYLATION AND ALDOL CONDENSATION OF CAMPHOR AND DERIVATIVES
Publication TypeJournal Article
Year of Publication1991
AuthorsHutchinson, JH, Li, DLF, Money, T, Palme, M, Agharahimi, MR, Albizati, KF
JournalCanadian Journal of Chemistry-Revue Canadienne De Chimie
Volume69
Pagination558-566
Date PublishedMar
Type of ArticleArticle
ISBN Number0008-4042
KeywordsAPPROACH, BICYCLO<2.2.1>HEPTANES, C(3)ALDOL, C(3)METHYLATION, CAMPHOR, NUCLEAR MAGNETIC-RESONANCE, ORGANIC-SYNTHESIS, PSEUDOGUAIANOLIDES, STEREOCONTROLLED, VITAMIN-D METABOLITES
Abstract

The stereoselectivity of methylation and aldol condensation of camphor and derivatives is determined by the presence or absence of a C(7) syn-methyl group and (or) C(5) and C(6) endo-hydrogen atoms.

URL<Go to ISI>://A1991FE80800029