@article { ISI:000244257400014,
	title = {Practical and facile approach towards indole alkaloids: (-)-mitralactonine},
	journal = {Synlett},
	number = {1},
	year = {2007},
	month = {JAN},
	pages = {79-82},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>An efficient approach to (-)-mitralactonine using Pictet-Spengler cyclisation with a highly functionalised masked aldehyde is described. Sharpless asymmetric dihydroxylation (SAD) is utilised to introduce chirality in the key substrate.</p>},
	keywords = {alkaloids, asymmetric, cyclisations, dihydroxylations, thioacetats},
	issn = {0936-5214},
	doi = {10.1055/s-2006-958434},
	author = {Chavan, Subhash P. and Sharma, Pallavi and Sivappa, Rasapalli and Kalkote, Uttam R.}
}
@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.}
}
