𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Structure of the product of the 1,3-dipolar cycloaddition of C-phenyl-N-(4-nitrophenyl)nitrilimine to 2-methyl-4-chlorophthalazone hydrazone

✍ Scribed by I. A. Litvinov; Yu. T. Struchkov; B. I. Buzykin; N. N. Bystrykh


Book ID
112447260
Publisher
Springer
Year
1982
Tongue
English
Weight
523 KB
Volume
31
Category
Article
ISSN
1573-9171

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Diastereoselective nitrilimine cycloaddi
✍ Giorgio Molteni; Gianluigi Broggini; Tullio Pilati πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 English βš– 255 KB

Enantiopure 1,4-benzodiazepin-4-one 1 and 1,4-benzodiazepin-6-ones 2 were reacted with hydrazonoyl chloride 8 in the presence of various basic agents. The diastereoselective 1,3-dipolar cycloaddition between the C N double bond of 1 or 2 and the nitrilimine intermediate 9 gave the enantiopure [1,2,4

ChemInform Abstract: 1,3-Dipolar Cycload
✍ Nivedita Acharjee; Avijit Banerji; Thierry Prange πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 28 KB πŸ‘ 2 views

## Abstract The catalytic effects of Lewis acids on the 1,3‐dipolar cycloaddition of nitrone (I) to benzylidene acetophenone (II) is studied.