BETA-LACTAMS FROM TETRAHYDRO-1,2-OXAZINE-3,6-DIONES, AND A LABELING STUDY OF THE PRODUCT STEREOCHEMISTRY

Authors
PROCTER G NALLY J ORDSMITH NHR
Citation
G. Procter et al., BETA-LACTAMS FROM TETRAHYDRO-1,2-OXAZINE-3,6-DIONES, AND A LABELING STUDY OF THE PRODUCT STEREOCHEMISTRY, Tetrahedron, 51(47), 1995, pp. 12837-12842
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
51
Issue
47
Year of publication
1995
Pages
12837 - 12842
Database
ISI
SICI code
0040-4020(1995)51:47<12837:BFTAAL>2.0.ZU;2-G
Abstract
The stereochemistry of the N-C bond-forming step in the photochemical conversion of a tetrahydro-1,2-oxazine-3,6-dione to a beta-lactam has been shown to rake place with scrambling of stereochemistry using a de uterium labelled precursor.