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Enantiopure Bicyclic Piperidinones: Stereoselectivity in Lactam Enolate Alkylations.

✍ Scribed by Andrew G. Brewster; Simon Broady; Catherine E. Davies; Thomas D. Heightman; Stephen A. Hermitage; Mark Hughes; Mark G. Moloney; Gordon Woods

Book ID
101963549
Publisher
John Wiley and Sons
Year
2004
Weight
206 KB
Volume
35
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

πŸ“œ SIMILAR VOLUMES

Diastereoselectivity in the alkylations
Diastereoselectivity in the alkylations of bicyclic piperidinones
✍ Catherine E. Mills (nΓ©e Davis); Thomas D. Heightman; Stephen A. Hermitage; Mark πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 260 KB

The synthesis of substituted [4.3.0] bicyclic iactams derived from 6-oxo-2-hydroxymethylpip~ridine is described. The enolate dm'ived f~om these systems can be alkylated with a range of reactive electrophiles; the diastereoselectivity which can be achieved depends on the substitution pattern of the o

ChemInform Abstract: Complementary Selec
ChemInform Abstract: Complementary Selectivity in the Alkylation of Chiral Bicyclic Lactam Enolates.
✍ G. P. ROTH; S. F. LEONARD; L. TONG πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 36 KB πŸ‘ 2 views

## 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 β€œFull Text” option. The original article is trackable v