Volume 27, Issue 11
Heterocyclic Compounds
Full Access

ChemInform Abstract: Highly Enantioselective Route to β-Lactams via Intramolecular C-H Insertion Reactions of Diazoacetylazacycloalkanes Catalyzed by Chiral Dirhodium(II) Carboxamidates.

M. P. DOYLE

M. P. DOYLE

Dep. Chem., Trinity Univ., San Antonio, TX 78212, USA

Search for more papers by this author
A. V. KALININ

A. V. KALININ

Dep. Chem., Trinity Univ., San Antonio, TX 78212, USA

Search for more papers by this author
First published: March 12, 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 carbenes obtained by decomposition of the diazoacetylazacycloalkanes (I), (III), and (VI) undergo highly enantioselective intramolecular C-H insertion reactions under conditions A) to form the corresponding β- and γ-lactams.

chemical structure image

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