Cyclization of 4-[Alkoxycarbonylmethylamino]- and 4-[Alkoxycarbonylmethylthio]-5-aminopyrrolo[2,3-d]pyrimidines to Give Azabenz[cd]azulenes
✍ Scribed by S. Tumkevicius; V. Masevicius
- Book ID
- 111558039
- Publisher
- Springer US
- Year
- 2003
- Tongue
- English
- Weight
- 101 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0009-3122
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📜 SIMILAR VOLUMES
## Abstract magnified image The cyclocondensation of 5‐hydroxy‐pyrido[2,3‐__d__]pyrimidines **1** with malonates gives pyrano[2′,3′:4,5]‐pyrido[2,3‐__d__]pyrimidines **2**. Nitration of **1** and reduction with zinc in the presence of carboxylic acids/anhydrides gave 2‐alkyloxazolo[5′,4′:4,5]pyrid
## Abstract Some new 7,9‐disubstituted 7__H__‐1,2,3,4‐tetrazolo[1,5‐__c__]pyrrolo[3,2‐__e__]pyrimidines 5 have been synthesized either by diazotization of 4‐hydrazino‐5,7‐disubstituted‐7__H__‐pyrrolo[2,3‐__d__]pyrimidines 4 obtained by hydrazinolysis of 4‐chloro‐5,7‐disubstituted‐7__H__‐pyrrolo[2,3