Carbanion induced synthesis of dibenzo[a,c]cycloheptenes through ring transformation reactions of 2H-pyran-2-one
โ Scribed by Vishnu Ji Ram; Nidhi Agarwal
- Book ID
- 104251352
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 141 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
An efficient and convenient one-pot synthesis of 4-aryl-2-methylsulfanyl-6,7-dihydro-5H-dibenzo[a,c]cycloheptene-1carboxylate 3a-n has been delineated and illustrated through carbanion induced ring transformation of 6-aryl-3-carbomethoxy-4methylsulfanyl-2H-pyran-2-ones 1 with benzosuberone 2.
๐ SIMILAR VOLUMES
A synthesis of unsymmetrical highly functionalized biaryls with an amino substituent juxtaposed with two nitrile groups in one of the phenyl rings is delineated and illustrated by the carbanion-induced ring-transformation of 6-aryl-4-methylsulfanyl-2H-pyran-2-one-3-carbonitrile (1) and 4-sec-amino-6
Pyrazolo[1,5-a]pyridines (3) and pyrano [4,3-d]pyrazolo [1,5-achieved from the reaction of 2 with polarised ketene dithioacetals (5) and arylidenemalononitrile, respectively. An a]pyridines (4) have been synthesized from the reaction of pyran-2-one (1) and 5-aryl-3-cyanomethyl-1H-pyrazole (2) analog