𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Studies on the mechanism of β-lactam formation

✍ Scribed by Ajay K. Bose; Y.H. Chiang; M.S. Manhas


Publisher
Elsevier Science
Year
1972
Tongue
French
Weight
177 KB
Volume
13
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Electrochemical studies on β-lactams. Pa
✍ Maria Antonietta Casadei; Achille Inesi; Franco Micheletti Moracci; Donatella Oc 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 547 KB

Electroreduction of 3-bromo-and 3,3-dichloro-JMzctams 1 carried out at the potential of the first voltammetricpeak andin thepresence of acetic anhydridegives3-acetyl-#-lactams2. The electrosynthesis is highly stereoselective, as only the acetyl derivative with trans co@iguration is formed.

On the mechanism and stereochemistry of
✍ Hong-Zhong Wang; Xin Zhou; Jia-Xi Xu; Sheng Jin; Yue-Ming Li; AlbertS. C. Chan 📂 Article 📅 2001 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 92 KB

## Abstract 2‐Chloro‐4‐phenyl‐2a‐(4′‐methoxyphenyl)‐3,5‐dihydroazatetracyclic [1,2‐__d__]benzo [ 1,4]diazepin‐1 ‐one (**III**~a~) and 2‐chloro‐4‐methyl‐2a‐(4′‐methoxyphenyl)‐3,5‐dihydroazatetracyclic[1,2‐__d__]‐benzo[1,4]diazepin‐1‐one (**III**~b~) were synthesized. 1‐Benzoyl‐2‐phenyl‐4‐(4′‐methoxy