𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Azabicyclobutanes. Formation of an azabicyclo[1.1.0]butane via irradiation of an allylic azide

✍ Scribed by Alfred G. Hortmann; Jack E. Martinelli


Publisher
Elsevier Science
Year
1968
Tongue
French
Weight
129 KB
Volume
9
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Oligomer formation via reactions of 3-et
✍ Alan P. Marchand; Sulejman AlihodΕΎiΔ‡ πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 707 KB

Electrophilic additions of arenesulfonyl azides (i.e., TsN3 and NsN3) to 3-ethyl-1-azabicycio-[1.1.0]butane (1) in CDCI3 at 80"C has been observed to result in the formation of oligomeric products. The mechanism of these reactions probably involves the formation of a carbocationic intermediate, i.e.

Novel efficient synthesis of 1-azabicycl
✍ Kazuhiko Hayashi; Chisato Sato; Shinsuke Hiki; Toshio Kumagai; Satoshi Tamai; Ta πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 216 KB

Novel efficient synthesis of 1-azabicyclo[1.1.0]butane and its application to the synthesis of 1.(1,3-thiazolin-2-yl)azetidine-3-thiol useful for the pendant moiety of an oral llS-methylcarbapenem antibiotic L-084