@article {46429,
	title = {Efficient and convenient route for the synthesis of thiophene-2-carboxamidines as potential inhibitors of nitric oxide synthase (NOS)},
	journal = {Tetrahedron Letters},
	volume = {60},
	year = {2019},
	month = {NOV},
	pages = {151254},
	type = {Article},
	abstract = {<p>A mild and efficient synthesis of substituted thiophene-2-carboxamidines which are potent inhibitors of nitric oxide synthase (NOS) is reported herein. The key step involves reaction of a BOC-protected imidazolyl thiophene-2-carboxamidine reactive intermediate with various primary amines to form BOC-thio-phene-2-carboxamidines which could be readily deprotected using TFA to furnish free carboxamidines. The method is very mild and tolerates diverse substituents including sensitive peptide and amino acid fragments. This new methodology represents a substantial improvement to the literature method owing to its simplicity and hassle-free purification procedures. (C) 2019 Elsevier Ltd. All rights reserved.</p>
},
	keywords = {Amidines, Nitric oxide synthase (NOS), Nitric oxide synthase inhibitors, Thiophene-2-carboxamidines},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2019.151254},
	author = {Rashid, P. P. and Singh, Dharmendra and Sanjayan, Gangadhar J.}
}
