Synthesis of 1,5-Benzodiazepine Nucleosides

dc.contributor.author	'ROSHAN AHMAD
dc.contributor.author	M. ZIA-UL-HAQ
dc.contributor.author	SHAHID HAMEED
dc.contributor.author	HUMAIRA NADEEM
dc.contributor.author	DUDDECK, HELMUT
dc.date.accessioned	2023-08-25T10:13:07Z
dc.date.available	2023-08-25T10:13:07Z
dc.date.issued	2000-12-04
dc.identifier.citation	Yadav, A. K., Kumar, M., Yadav, T., & Jain, R. (2010). A novel one pot room temperature ionic liquid mediated synthesis of 1, 5-benzodiazepine ribofuranosides.	en_US
dc.identifier.issn	0253-5106
dc.identifier.uri	http://142.54.178.187:9060/xmlui/handle/123456789/19562
dc.description.abstract	The phenolic beta -diketones I prepared by modified Baker-Venkataraman rearrangement were converted to benzodiazepine derivatives II by treatment with o-phenylenediamine. Coupling of benzodiazepine derivatives II with acetobromo sugars in presence of mercuric cyanide and nitromethane gave acetylated sugar derivatives of benzodiazepines III. The nucleosides IV were obtained by the deacetylation of compounds III. Structures of all intermediates and final products were confirmed with the help of modern spectroscopic methods.	en_US
dc.description.sponsorship	The chemical society of Pakistan is an approved society from the PSF	en_US
dc.language.iso	en	en_US
dc.publisher	Karachi: International Centre for Chemical and Biological Sciences, H.E.J. Research Institute of Chemistry, University of Karachi	en_US
dc.title	Synthesis of 1,5-Benzodiazepine Nucleosides	en_US
dc.type	Article	en_US