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Title: New synthesis of 5,6-benzindole

Journal Article · · Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00486910· OSTI ID:7160065

A method has been developed for the synthesis of linear 5,6-benzindole by reduction of N-acetyl-5,6-benzindoxy with NaBH/sub 4/ and subsequent hydrolysis of the N-acetyl group. The PMR spectra were obtained on a Varian H-100 spectrometer in solutions of acetone-d/sub 6/ and chloroform-d/sub 3/ with TMA as internal standard. IR spectra were recorded on a Perkin-Elmer 180 spectrometer in KBr disks or in chloroform solutions in standard cells. TLC was conducted on Silufol UV-254 plates, with chloroform as eluent.

Research Organization:
Institute of Biophysics, Moscow (USSR)
OSTI ID:
7160065
Journal Information:
Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Vol. 23:6; Other Information: Translated from Khim. Geterotsikl. Soedin.; 23: No. 6, 779-780(Jun 1987)
Country of Publication:
United States
Language:
English

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