๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Structure of a carbocyclic oxapenam analogue

โœ Scribed by Sheldrick, B. ;Akrigg, D. ;Page, M. I. ;Agathocleous, D.


Book ID
114503289
Publisher
International Union of Crystallography
Year
1985
Tongue
English
Weight
202 KB
Volume
41
Category
Article
ISSN
0108-2701

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Stereochemistry and ring opening of a ca
โœ Demetrios Agathocleous; Graham Cox; Michael I Page ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 173 KB

The cycloaddition of succinimido ketene to 2,3\_dihydrofuran yields 7-exo-succinimido bicycle C3.2.01 2-oxoheptan-6-one. This unusual stereo-chemistry is confirmed by 'H NMR and X-ray crystallography. The cyclobutanone product undergoes ring opening in concentrated hydrochloric acid to give 1-succin

Structure of a carbocyclic analogue of p
โœ Sheldrick, B. ;Akrigg, D. ;Page, M. I. ;Agathocleous, D. ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› International Union of Crystallography ๐ŸŒ English โš– 301 KB
Synthesis of a novel bicyclic ฮณ-lactam a
โœ Jack E. Baldwin; Richard T. Freeman; Christopher Schofield ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 139 KB

A succinct synthesis of a new bicyclic y-lactam designed to possess antibacterial activity containing an oxazolidine ring is described.