Synthesis of 5-amino-4-(cyanoformimidoyl)-1H-imidazole: a reactive intermediate for the synthesis of 6-carbamoyl-1,2-dihydropurines and 6-carbamoylpurines-Reference-Cited by-同舟云学术

Synthesis of 5-amino-4-(cyanoformimidoyl)-1H-imidazole: a reactive intermediate for the synthesis of 6-carbamoyl-1,2-dihydropurines and 6-carbamoylpurines

Published:1990 Issue:6 Volume: Page:1705-1712
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Alves M. José,Booth Brian L,Proenç M. Fernanda J. R. P.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1990/P1/P19900001705

Reference8 articles.

1. The chemistry of nitrilium salts. Part 4. Some reactions of 5-amino-4(C-cyanoformimidoyl)imidazoles obtained from nitrilium trifluoromethanesulphonate salts and diaminomaleonitrile

2. Synthesis of 6-Cyanopurines from 5-Amino-4-(cyanoformimidoyl)-1,2-dimethylimidazole

3. Chemistry of hydrocyanic acid. 1. Formation and reactions of N-(aminomethylene)diaminomaleonitrile, a hydrocyanic acid pentamer and precursor to adenine

4. A. B. Voet and A. W.Schwartz, in ‘Origin of Life,’ ed. Y. Wolman, Reidel, Amsterdam, 1981;

5. HCN and chemical evolution: The possible role of cyano compounds in prebiotic synthesis

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