Volume 27, Issue 23
Natural Products
Full Access

ChemInform Abstract: Synthesis of Carbocycles via Intramolecular Conjugate Additions: Total Syntheses of Axane Sesquiterpenoids.

A.-C. GUEVEL

A.-C. GUEVEL

Dep. Chem., Ohio State Univ., Columbus, OH 43210, USA

Search for more papers by this author
D. J. HART

D. J. HART

Dep. Chem., Ohio State Univ., Columbus, OH 43210, USA

Search for more papers by this author
First published: June 4, 1996

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The key steps in the synthesis of the sesquiterpenoids (VIII)-(X) are highly diastereoselective intramolecular cyclization of the unsaturated ester (II) yielding the perhydroindan (III) and a series of cerium-mediated olefinations.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.