EventsThe 3rd International Electronic Conference on Synthetic Organic Chemistry
Event submissions
Published
with-doi10.3390/ecsoc-3-01735
This submission belongs to the session a. General Organic Synthesis of the event The 3rd International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 1999
Citation
Nazaret Arias, M. Carmen Fernandez, M. Pilar Vazquez Tato, Julio A. Seijas, Microwave Enhanced Knoevenagel Reaction: an expeditious method to prepare 3-benzylidene-1,3-dihydroindol-2-ones, in Proceedings of The 3rd International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1999, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-3-01735
Share
Email
Facebook
Twitter
LinkedIn

Microwave Enhanced Knoevenagel Reaction: an expeditious method to prepare 3-benzylidene-1,3-dihydroindol-2-ones

Julio A. Seijas 1
M. Pilar Vazquez Tato 1
M. Carmen Fernandez 1
Nazaret Arias 1
1. Departamento de Quimica Organica. Universidad de Santiago de Compostela. Facultad de Ciencias. Aptdo. 280. 27080-Lugo. Spain
Abstract
Knoevenagel reaction has been object of a complete study1, recently the enhancement of this reaction by microwave heating has been reported by several groups2. We became interested in 3-benzylidene-1,3-dihydroindol-2-ones, as they have been reported as natural products from Isatis indigotica3, although they have been known as pharmacological agents from several years4.
Keywords
n/a
Microwave Enhanced Synthesis of Quinazolines.
Hydroamination of Cinnamyl Alcohol