@article { ISI:000359134700008,
	title = {Efficient one pot regioselective synthesis of a 3,3 {\textquoteleft}-spiro-phosphonylpyrazole-oxindole framework via base mediated [1,3]-dipolar cycloaddition reaction of the Bestmann-Ohira reagent with methyleneindolinones},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {13},
	number = {32},
	year = {2015},
	month = {JUL},
	pages = {8669-8675},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A one pot, highly regioselective synthesis of racemic 3,3{\textquoteright}-spiro-phosphonylpyrazole-oxindole by 1,3-dipolar cycloaddition of an in situ generated anion of dialkyl 1-diazomethylphosphonate from the Bestmann-Ohira reagent (BOR) \&amp; methyleneindolinones has been developed. The synthesis affords the highly functionalized pyrazole scaffolds in good yields with excellent regioselectivity under mild reaction conditions within a short reaction time.</p>},
	issn = {1477-0520},
	doi = {10.1039/c5ob01020a},
	author = {Shelke, Anil M. and Suryavanshi, Gurunath}
}
@article { ISI:000363828500010,
	title = {Efficient organocatalytic route for asymmetric total synthesis of stagonolide F},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {45},
	year = {2015},
	month = {NOV},
	pages = {6207-6209},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A stereoselective total synthesis of Stagonolide F (98\% ee) is described employing asymmetric alpha-aminooxylation, Jorgensen{\textquoteright}s asymmetric epoxidation, Brown asymmetric allylation, Steglich esterification and ring closing metathesis as key steps. The use of organocatalytic alpha-aminooxylation and Jorgensen{\textquoteright}s asymmetric epoxidation of aldehydes for the introduction of chirality makes this approach more attractive. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {alpha-Aminooxylation, Jorgensens{\textquoteright}s asymmetric epoxidation, Macrolide, Ring-closing metathesis, Total synthesis},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.09.082},
	author = {Shelke, Anil M. and Suryavanshi, Gurunath}
}
@article {43539,
	title = {Efficient Sn(II)-catalyzed one-pot synthesis of a 3-substituted azetidine-2,4-dione framework},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {15},
	year = {2017},
	month = {MAR},
	pages = {2385-2391},
	abstract = {A novel Sn(II)-catalyzed tandem cyclization reaction of aromatic aldehydes with ethyl cyanoacetate has been achieved to afford a series of 3-substituted azetidine-2,4-diones in good to excellent yields. This protocol provides straightforward access to construct the azetidine core through sequential Knoevenagel condensation, hydration and the C-N cyclization reaction.},
	doi = {10.1039/c7ob00294g},
	author = {Chavan, Santosh S. and Supekar, Mrudul V. and Burate, Pralhad A. and Rupanwar, Bapurao D. and Shelke, Anil M. and Suryavanshi, Gurunath}
}
