@article { ISI:000304851500040,
	title = {Sugar-amino acid cyclic conjugates as novel conformationally constrained hydroxyethylamine transition-state isosteres},
	journal = {Tetrahedron Letters},
	volume = {53},
	number = {26},
	year = {2012},
	month = {JUN},
	pages = {3361-3363},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Hydroxyethylamine (HEA) isosteres have previously been shown to display a multitude of biomedical applications. In fact, the first protease inhibitor, saquinavir is an HEA based peptidomimetic. Herein we describe an easy-to-operate synthetic route to a series of carbohydrate-based conformationally constrained hydroxyethylamine (HEA) isosteres featuring amino acid side chains, starting from D-glucose. This class of novel sugar-amino acid-tethered conformationally restricted HEA systems may have bearing in practical application, particularly in the development of conformationally restricted protease inhibitors. (C) 2012 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Conformationally constrained, D-Glucose, hydroxyethylamine isosteres, protease inhibitor, Reductive amination},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2012.04.086},
	author = {Roy, Arup and Sanjayan, Gangadhar J.}
}
@article {49257,
	title = {Biocatalysis enables the scalable conversion of biobased furans into various furfurylamines},
	journal = {NATURE COMMUNICATIONS},
	volume = {15},
	year = {2024},
	month = {JUL },
	type = {Journal Article},
	keywords = {Biomass, OMEGA-TRANSAMINASE, OXIDASE, Reductive amination, SPECIFICITY},
	doi = {10.1038/s41467-024-50637-x},
	author = {Giri, Pritam and Lim, Seonga and Khobragade, Taresh P. and Pagar, Amol D. and Patil, Mahesh D. and Sarak, Sharad and Jeon, Hyunwoo and Joo, Sangwoo and Goh, Younghwan and Jung, Seohee and Jang, Yu-Jeong and Choi, Seung Beom and Kim, Ye Chan and Kang, Taek Jin and Heo, Yong-Seok and Yun, Hyungdon}
}
