Reaction between 5-Benzylidene-2,2-Dimethyl-1,3-Dioxane-4,6-Dione and Tert-butyl Isocyanide in the Presence of Ethane-1,2-diol or Catechol

doi:10.3184/030823407X198401

Paper

Reaction between 5-Benzylidene-2,2-Dimethyl-1,3-Dioxane-4,6-Dione and Tert-butyl Isocyanide in the Presence of Ethane-1,2-diol or Catechol

Published Mar 1, 2007 · I. Yavari, H. Zare, B. Mohtat

Journal of Chemical Research

Q3 SJR score

3

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

tert-Butyl isocyanide undergoes a smooth reaction with 5-benzylidene-2,2-dimethyl-1,3-dioxane-4,6-diones (benzylidene Meldrum's acids) in the presence of ethane-1,2-diol or catechol to produce functionalised N-tert-butyl-2-(5,7-dioxo-1,4-dioxepane-6-yl)-2-aryl-ethanamides or bis-(2-hydroxyphenyl) 2-[2-(tert-butylamino)-1-aryl-2-oxoethyl]-malonates in good yields.

Study Snapshot

Tert-butyl isocyanide effectively reacts with 5-benzylidene-2,2-dimethyl-1,3-dioxane-4,6-diones to produce functionalized N-tert-butyl-2-(5,7-dioxo-1,4

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Sign up to use Study Snapshot

Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.

Create an account

Paper

Reaction between 5-Benzylidene-2,2-Dimethyl-1,3-Dioxane-4,6-Dione and Tert-butyl Isocyanide in the Presence of Ethane-1,2-diol or Catechol

Sign up to use Study Snapshot

References

Citations

A novel and efficient strategy for the synthesis of various carbamates using carbamoyl chlorides under solvent-free and grinding conditions using microwave irradiation

This study presents an efficient, fast, and simple strategy for synthesising various carbamate derivatives using carbamoyl chlorides under solvent-free conditions using microwave irradiation, without hazardous phosgene.