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Regioselective Unusual Formation of Spirocyclic 4-{2‘-Benzo(2‘,3‘-dihydro)furo}- 9-methyl-2,3,9-trihydrothiopyrano[2,3- b ]indole by 4 -exo-trig Aryl Radical Cyclization and Rearrangement

✍ Scribed by Majumdar, K. C.; Alam, S.

Book ID
127270205
Publisher
American Chemical Society
Year
2006
Tongue
English
Weight
114 KB
Volume
8
Category
Article
ISSN
1523-7060

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📜 SIMILAR VOLUMES

Regioselective unusual formation of spir
Regioselective unusual formation of spirocyclic 4-{3′-benzo(2′,3′-dihydro)furo}-9-methyl-2,3,9-trihydrothiopyrano [2,3-b]indole by acid-catalyzed reaction of enol ethers
✍ K. C. Majumdar; S. Alam; B. Chattopadhyay 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 143 KB

## Abstract magnified image Spirocyclic 4‐{3′‐benzo(2′,3′‐dihydro)furo}‐9‐methyl‐2,3,9‐trihydrothiopyrano[2,3‐__b__]indoles are regioselectively synthesized by treating suitable enol ethers, 4‐aryloxymethylene‐9‐methyl‐2,3,9‐trihydrothio‐pyrano[2,3‐__b__]indoles with H~2~SO~4~ in dichloromethane‐m

ChemInform Abstract: Regioselective Unus
ChemInform Abstract: Regioselective Unusual Formation of Spirocyclic 4-{3′-Benzo(2′,3′-dihydro)furo}-9-methyl-2,3,9-trihydrothiopyrano [2,3-b]indole by Acid-Catalyzed Reaction of Enol Ethers.
✍ K. C. Majumdar; S. Alam; B. Chattopadhyay 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 38 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v