@article { ISI:000233052200016,
	title = {O-H center dot center dot center dot O-bridged dimers linked via C-H center dot center dot center dot O and C-H center dot center dot center dot pi interactions in 4,6-di-O-benzyl-myo-inositol 1,3,5-orthoformate},
	journal = {Acta Crystallographica Section C-Crystal Structure Communications},
	volume = {61},
	number = {11},
	year = {2005},
	month = {NOV},
	pages = {O628-O630},
	publisher = {BLACKWELL PUBLISHING},
	type = {Article},
	address = {9600 GARSINGTON RD, OXFORD OX4 2DQ, OXON, ENGLAND},
	issn = {0108-2701},
	doi = {10.1107/S0108270105029422},
	author = {Manoj, Kochunnoonny and Devaraj, Subramanian and Gonnade, Rajesh G. and Bhadbhade, Mohan M. and Shashidhar, M. S.}
}
@article {43798,
	title = {Organocatalytic enantioselective vinylogous michael-aidoi cascade for the synthesis of spirocyclic compounds},
	journal = {Organic Letters},
	volume = {19},
	year = {2017},
	month = {AUG},
	pages = {4367-4370},
	type = {Article},
	abstract = {Enantioselective synthesis of pyrazolone-fused spirocyclohexenols by the secondary amine-catalyzed cascade reaction of alpha,beta-unsaturated aldehydes with alpha-arylidene pyrazolinones is reported. This formal [3 + 3] organocascade reaction proceeds through a vinylogous Michael-aldol sequence to furnish the spiroheterocycles with three stereocenters including an all-carbon quaternary center in good yields and selectivities. The catalytic generation of alpha,beta-unsaturated iminium ions from enals and tandem dienolate/enolate formation from pyrazolinones are the key for the success of this spiroannulation reaction.},
	doi = {10.1021/acs.orglett.7b02085},
	author = {Mondal, Santigopal and Mukherjee, Subrata and Yetra, Santhivardhana Reddy and Gonnade, Rajesh G. and Biju, Akkattu T.}
}
@article {45473,
	title = {Organocatalytic asymmetric cascade reaction of gamma-substituted deconjugated butenolides with o-formyl-beta-nitrostyrene},
	journal = {ChemistrySelect},
	volume = {3},
	year = {2018},
	month = {JUL},
	pages = {8189-8192},
	type = {Article},
	abstract = {<p>An efficient chemo-, diastereo- and enantio-selective cascade synthesis of functionalized indanols bearing four contiguous stereogenic centres has been developed via the reaction of beta,gamma-butenolides with o-formyl-beta-nitrostyrenes in the presence of bi-functional hydrogen-bonding catalyst. Indanol derivatives containing gamma,gamma-disubstituted butenolides were obtained in good yields and with moderate to high enantioselectivities/diastereoselectivities.</p>},
	keywords = {butenolides, Cascade reaction, Enantioselectivity, Indanol, organocatalysis},
	issn = {2365-6549},
	doi = {10.1002/slct.201801467},
	author = {Deepake, Siddharth K. and Lanjewar, Atul B. and Thatikonda, Thanusha and Gonnade, Rajesh G. and Das, Utpal}
}
@article {48681,
	title = {Organocatalysed one-pot three component synthesis of 3,3'-disubstituted oxindoles featuring an all-carbon quaternary center and [spiro 2H-pyran-3,4'-indoline]},
	journal = {RSC Advances},
	volume = {13},
	year = {2023},
	month = {APR},
	pages = {13206-13212},
	type = {Article},
	abstract = {<p>
	A simple and efficient methodology for the one-pot synthesis of 3,3 {\textquoteleft}-disubstituted oxindoles featuring an all-carbon quaternary center has been demonstrated through l-proline catalysed three-component reaction based on sequential Knoevenagel condensation/Michael addition and also one-pot synthesis of spiro[2H-pyran-3,4 {\textquoteleft}-indoline] through consecutive Knoevenagel condensation/Michael addition/reduction/cyclization reactions from readily available isatin derivatives, malononitrile, and ketones. The present methodology presents several advantages, including simple reaction set-up, short reaction times, and easy to work-up. Also, this strategy offers broad substrate scope with excellent yields and high atom economy, under mild reaction conditions.</p>
},
	doi = {10.1039/d3ra00510k},
	author = {Nichinde, Chandrakant B. and Patil, Baliram R. and Chaudhari, Suryakant S. and Mali, Bhupendra P. and Gonnade, Rajesh G. and Kinage, Anil K.}
}
