## Abstract magnified image 2‐Methyl‐2,5,6,11,12,13‐hexahydro 4H indazolo[5,4‐a]pyrrolo[3,4‐c]carbazole‐4‐one was synthesized utilizing a regioselective Diels‐Alder reaction with 5‐(1H‐indol‐2‐yl)‐2‐methyl‐6,7‐dihydro‐2H‐indazole and ethyl __cis__‐β‐cyanoacrylate. Acetic acid and YtBr~3~ were the b
ChemInform Abstract: Regioselective Synthesis of 2-Methyl-2,5,6,11,12,13-hexahydro 4H Indazolo[5,4-a]pyrrolo[3,4-c]carbazole-4-ones.
✍ Scribed by Ming Tao; Chung Ho Park; Kurt Josef; Robert L. Hudkins
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 45 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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📜 SIMILAR VOLUMES
Hexahydro-4a-methyl-7,7-diphenyl-1(2H)-naphthalenone. -A clean and efficient route to the hitherto not reported title compound (VIII) starting from the known 3-ethenylcyclohexanone (I) is given. The approach represents a general strategy for the synthesis of related 7,7-diarylhexahydronaphthalenone