Hydride-abstraction reactions from cycloheptatriene and 1-carbamoylcycloheptatriene. Effect of the CONH2 group orientation on the reactivity difference of the exo and endo hydrogen toward hydride abstraction. A quantum-chemical study
- 1 March 1983
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 105 (5) , 1284-1288
- https://doi.org/10.1021/ja00343a034
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- The hydride-donation reaction of reduced nicotinamide adenine dinucleotide. 2. MINDO/3 and STO-3G calculations on the role of the carbamoyl group in enzymic reactionsJournal of the American Chemical Society, 1981
- Hydride-donation reaction of reduced nicotinamide adenine dinucleotide. 1. MINDO/3 and STO-3G calculations on analog reactions with cyclopropene, tropylidene, and 1,4-dihydropyridine as hydride donors and the cyclopropenium cation as acceptorJournal of the American Chemical Society, 1981