@article { ISI:000349061500011,
	title = {Formal syntheses of (2R,3R)-3-hydroxy pipecolic acid and (2R,3S)-3-hydroxy pipecolic acid from L-ascorbic acid},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {6},
	year = {2015},
	month = {FEB},
	pages = {805-807},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Formal syntheses of both cis and trans 3-hydroxy pipecolic acids is achieved from L-ascorbic acid. Present synthesis describes use of chiral pool approach in which epimerization, Staudinger reaction and Cyclization reactions were employed as key steps. (C) 2014 Elsevier Ltd. All rights reserved.</p>},
	keywords = {3-Hydroxy pipecolic acid, cyclization, Epimerization, L-Ascorbic acid},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2014.12.103},
	author = {Chavan, Subhash P. and Dumare, Nilesh B. and Pawar, Kailash P.}
}
@article {49898,
	title = {Formal Synthesis of Corynanthe Indole Alkaloid ({\textpm})-Mitralactonine: Construction of α-Hydroxy-Keto Functionalized Tetracyclic Skeleton},
	journal = {Chemistryselect},
	volume = {10},
	year = {2025},
	month = {DEC },
	pages = {e04415},
	type = {Article},
	abstract = {<p>
	An efficient synthesis of a tetracyclic skeleton common to many corynanthe alkaloids was accomplished in 10 linear steps starting from a known tetrahydro beta-carboline intermediate. The tetracyclic alpha-hydroxy keto functionalized advanced precursor of (+/-)-mitralactonine was realized using Wittig olefination, ketohydroxylation of a trisubstituted alkene, and a tandem amine unmasking-intramolecular nucleophilic displacement reaction for C-N bond formation of C/D-rings.</p>
},
	keywords = {alpha-hydroxy keto, beta-carboline, corynanthe alkaloid, intramolecular N-alkylation, mitragynine},
	issn = {2365-6549},
	doi = {10.1002/slct.202504415},
	author = {Dumare, Nilesh B. and Sharma, Pallavi and Sivappa, Rasapalli and Chavan, Subhash P.}
}
