๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Stereochemistry of the lithium-ammonia reduction of cis-1,7-dimethyltricyclo[4.4.0.02,6]decan-3-one and related compounds

โœ Scribed by Piers, Edward; Worster, Paul M.

Book ID
126998586
Publisher
American Chemical Society
Year
1972
Tongue
English
Weight
367 KB
Volume
94
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Reductive cleavage of 1-methyltricyclo[4
Reductive cleavage of 1-methyltricyclo[4.4.0.02,6]Decan-3-one and related compounds with lithium in liquid ammonia
โœ Drury Caine; William R. Pennington; Troy L. Smith Jr. ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 288 KB

Reductive cleavage of the external(a.8) bond of the cyclopropane ring in tricyclo[x.y.O.O \*,x9\_ alkan-3-ones with lithium in liquid ammonia provides a general method of synthesis of spirocyclic ketones. \*,3 Piers and Worster have recognized that the stereochemical fate of the S carbon atom is an

The reaction of 1-methyltricyclo [4.4.0.
The reaction of 1-methyltricyclo [4.4.0.02,6decaN-3-one and related compounds with hydrogen bromide in acetic acid
โœ Drury Caine; Anibal A. Boucugnani; Chia-Yeh Chu; Samuel L. Graham; Troy L. Smith ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 260 KB

In recent years there has been considerable interest in the mode of cleavage of conjugated cyclopropyl ketones with electrophilic reagents. 2 l-Methyltricyclol4.4.0.0 2'6]decan-3-one(&,) and derivatives which have both 8 carbons of the cyclopropane ring fully substituted in principle can give Spiro