@article { ISI:000380599800018,
	title = {Multi-gram scale synthesis of hunanamycin A, an antibiotic natural product from the marine source},
	journal = {Tetrahedron Letters},
	volume = {57},
	number = {32},
	year = {2016},
	month = {AUG},
	pages = {3662-3663},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A simple, practical, and biomimetic approach to access antibiotic natural product hunanamycin A starting from readily available inexpensive material Riboflavin is disclosed here. The present synthesis consists of three operationally simple, protecting group free steps and it is far superior when compared with the previous route. Using this route one can make multi-gram quantities of the natural product which will help in further biological assays, in particular exploring the potential of treating food infections. (C) 2016 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Antibacterial, Biomimetic synthesis, Gram scale synthesis, Natural product, Riboflavin},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2016.07.003},
	author = {Shingare, Rahul D. and Farhana, Sa Ada and Reddy, D. Srinivasa}
}
@article {48718,
	title = {Rapid bioinspired N-acyliminium ion strategy for the ABC core of the stemona alkaloids},
	journal = {Asian Journal of Organic Chemistry},
	volume = {12},
	year = {2023},
	month = {SEP},
	type = {Article},
	abstract = {<p>
	A concise and highly diastereoselective bioinspired key cationic cyclization strategy for the asymmetric synthesis of the tricyclic core of the (-)-stemoamide, together with 8,9-bis-epi-stemoamide has been described. The key N-acyliminium ion precursors were accessed from L-tartaric acid and L-malic acid respectively. The use of ethyl acetoacetate derived bifunctional allylidenetriphenylphosphorane reagent in the early stage of the synthetic strategy is advantageous for the rapid construction of highly functionalized key pyrrolo[1,2-\&amp; alpha;]azepine frameworks.</p>
},
	keywords = {alkaloids, Biomimetic synthesis, Claisen rearrangement, cyclization, Regioselectivity},
	issn = {2193-5807},
	doi = {10.1002/ajoc.202300331},
	author = {Chavan, Subhash P. and Kalbhor, Dinesh B. and Gonnade, Rajesh G.}
}
