𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Microwave-Assisted Cycloaddition Reactions

✍ Scribed by Prasad Appukkuttan; Vaibhav P. Mehta; Erik V. van der Eycken

Publisher
John Wiley and Sons
Year
2010
Weight
15 KB
Volume
41
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Microwave-Assisted
ChemInform Abstract: Microwave-Assisted 1,3-Dipolar Cycloaddition Reactions of Nitrilimines and Nitrile Oxides.
✍ Hafida Kaddar; Jack Hamelin; Hadj Benhaoua πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 27 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: 1,3-Dipolar Cycload
ChemInform Abstract: 1,3-Dipolar Cycloaddition Reactions Assisted by Microwave Radiation and Gamma Radiation.
✍ Radhika S. Kusurkar; Uma D. Kannadkar πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: Studies on Chromone
ChemInform Abstract: Studies on Chromone Derivatives: Microwave Assisted 1,3-Dipolar Cycloaddition Reactions of 4-Oxo-1-benzopyran-3-carboxaldehyde Imine Oxides.
✍ A. H. KALITA; A. BORUAH; D. PRAJAPATI; J. S. SANDHU πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 1 views

Studies on Chromone Derivatives: Microwave Assisted 1,3-Dipolar Cycloaddition Reactions of 4-Oxo-1-benzopyran-3-carboxaldehyde Imine Oxides. -The title reaction using microwaves (2450 MHz) gives higher yields and needs shorter reaction times compared to the thermal cycloaddition (45-60%, 12-48 h).