𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Unprecedented 1,3-dipolar cycloaddition of azomethine ylides to ester carbonyl

✍ Scribed by Novikov, Mikhail S.; Voznyi, Igor V.; Khlebnikov, Alexander F.; Kopf, Jürgen; Kostikov, Rafael R.


Book ID
121319476
Publisher
Royal Society of Chemistry
Year
2002
Weight
117 KB
Volume
14
Category
Article
ISSN
1472-7781

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Unprecedented 1,3-Dipolar Cycloaddition
✍ Mikhail S. Novikov; Alexander F. Khlebnikov; Adolf Krebs; Rafael R. Kostikov 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 363 KB 👁 1 views

Iminiodifluoromethanides generated by the reaction of di-undergo regioselective 1,3-dipolar cycloaddition to aldehydes to give oxazolidine derivatives. fluorocarbene with benzaldehyde and benzophenone imines

1,3-Dipolar Cycloadditions of Phenanthri
✍ Jiří Dostál; Milan Potáček; Otakar Humpa; JaromÍR Marek 📂 Article 📅 2010 🏛 Wiley (John Wiley & Sons) ⚖ 399 KB 👁 1 views

## Abstract Azomethine ylides generated from 5‐(alkoxycarbonylmethyl)phenanthridinium cations were studied in 1,3‐dipolar cycloadditions with dimethyl maleate and dimethyl fumarate as dipolarophiles. The cycloadducts with the pyrrolidino[1,2‐f]phenanthridine skeleton easily underwent dehydrogenatio