@article { ISI:000242873400029,
	title = {Ring closing metathesis approach to the indole alkaloid mitralactonine},
	journal = {Tetrahedron Letters},
	volume = {47},
	number = {52},
	year = {2006},
	month = {DEC},
	pages = {9301-9303},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient utilisation of RCM leading to a convenient synthesis of a pentacyclic indole alkaloid is described. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	keywords = {corynanthe type alkaloid, Dihydroxylation, mitralactonine, RCM, Swern oxidation},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.10.106},
	author = {Chavan, Subhash P. and Sharma, Pallavi and Sivappa, R. and Kalkote, Uttam R.}
}
@article { ISI:000247620500052,
	title = {Total synthesis of pulchellalactam via an RCM strategy},
	journal = {Synthetic Communications},
	volume = {37},
	number = {7-9},
	year = {2007},
	month = {MAY},
	pages = {1503-1510},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>Total synthesis of (Z) pulchellalactam, a CD protein tyrosine phosphatase inhibitor, from commercially available methallyl chloride employing ring-closure metathesis (RCM) as a key step is described.</p>},
	keywords = {alkaloid, Natural products, pulchellalactam, RCM, Total synthesis},
	issn = {0039-7911},
	doi = {10.1080/00397910701229131},
	author = {Chavan, Subhash P. and Pathak, Ashok B. and Dhawane, Abasaheb N. and Kalkote, Uttam R.}
}
@article {47672,
	title = {Total synthesis of a hypothetical macroketone of migrastatin},
	journal = {European Journal of Organic Chemistry},
	volume = {2021},
	year = {2021},
	month = {JUN },
	pages = {3050-3053},
	type = {Article},
	abstract = {Danishefsky{\textquoteright}s macroketone, a simplified analogue of natural product Migrastatin, is one of the lead compounds with potent cancer cell migration inhibition potential. Different biological assays suggest fascin protein as the potential target. Although it was indicated through X-ray co-crystallography where the concerned macroketone analogue was found to bind in the actin-binding sites of fascin, there was a structural discrepancy, as the X-ray co-crystal structure suggested an E-olefin along with inversion of methyl stereochemistry from that of Danishefsky{\textquoteright}s macroketone. Here, we have accomplished the total synthesis of the {\textquoteleft}hypothetical macroketone{\textquoteright} for the first time. The TiCl4 mediated vinylogous Mukaiyama aldol reaction is the key step in present synthesis.},
	keywords = {Hypothetical mecroketon, Metastasis, Migrastatin, RCM, vinylogous Mukaiyama aldol reaction (VMAR)},
	issn = {1434-193X},
	doi = {10.1002/ejoc.202100484},
	author = {Choudhury, Rahul and Reddy, D. Srinivasa}
}
