𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Rearrangements of 1-Phenyl-1,2,3-Triazoles Bearing a Hydrazone or Oxime Function at the 4-Position

✍ Scribed by Gerrit L'abbé; Gonda van Essche; Pieter Delbeke; Suzanne Toppet


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
97 KB
Volume
99
Category
Article
ISSN
0037-9646

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Deformed Phthalocyanines: Synthesis and
✍ Takamitsu Fukuda; Shigetsugu Homma; Nagao Kobayashi 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 408 KB

## Abstract The synthesis of a series of zinc phthalocyanines partially phenyl‐substituted at the 1‐, 4‐, 8‐, 11‐, 15‐, 18‐, 22‐, and/or 25‐positions (the so‐called α‐positions) is reported. Macrocycle formation based on 3,6‐diphenylphthalonitrile, __o__‐phthalonitrile, and zinc acetate predominant

Density functional analysis of a decompo
✍ Peter Politzer; M. Edward Grice; Jorge M. Seminario 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 1 views

A density functional computational study shows that 4-nitro-1,2,3-triazole, which is highly impact sensitive, can decompose through ring opening and subsequent N 2 evolution, with the net release of 12 kcalrmol. An input of 52 kcalrmol is required to initiate the process. ᮊ 1997 John Wiley & Sons, I