𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Organomercury Carbenoids for the Synthesis of Cyclopropane Derivatives

✍ Scribed by Prof. Dr. Rolf Scheffold; Urs Michel


Publisher
John Wiley and Sons
Year
1972
Tongue
English
Weight
250 KB
Volume
11
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Stereoselective Syn
✍ S. NESET; H. HOPE; K. UNDHEIM πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB

Stereoselective Synthesis of Cyclopropane-1,2-bis(glycine) Derivatives. -The synthesis of the title compounds (VII) and (VIII) is achieved via stereoselective azidation of the trans-cyclopropane derivative (III). Interestingly, under similar conditions the cis-isomer (IX) reacts differently yieldin

On the Mechanism and Stereochemistry of
✍ Zhuofeng Ke; Yubing Zhou; Hui Gao; Cunyuan Zhao; Davidβ€…Lee Phillips πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 273 KB

## Abstract An investigation into the mechanism and stereochemistry of chiral lithium‐carbenoid‐promoted cyclopropanation reactions by using density functional theory (DFT) methods is reported. Previous work suggested that this type of cyclopropanation reaction may proceed by competition between a