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Rearrangement of the semidine type in the indole series. Synthesis of 2-arylamino-3-acetamidoindoles

✍ Scribed by G. N. Kurilo; N. I. Rostova; A. A. Cherkasova; A. N. Grinev


Book ID
112325340
Publisher
Springer US
Year
1977
Tongue
English
Weight
297 KB
Volume
13
Category
Article
ISSN
0009-3122

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Regioselective synthesis of 4-aryloxymet
✍ K. C. Majumdar; S. Alam; S. Muhuri πŸ“‚ Article πŸ“… 2007 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 345 KB

## Abstract magnified image A number of new 4‐aryloxymethylene‐2,3,5‐trihydrothiopyrano[3,2‐__b__]indoles are regioselectively synthesized in 78‐84% yield by the __thio__‐Claisen rearrangement of 3‐(4′‐aryloxybut‐2′‐ynylthio)indoles. The endocyclic double bonded products are isolated by introducin