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Catalytic asymmetric carbon–carbon bond-forming reactions in aqueous media
Tetrahedron: asymmetry, 2011-12, Vol.22 (23), p.1945-1979
2011
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Water: the most versatile and nature’s friendly media in asymmetric organocatalyzed direct aldol reactions
Tetrahedron: asymmetry, 2015-12, Vol.26 (21-22), p.1215-1244
2015
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Self-Assembly of Amphiphilic Dipeptide with Homo- and Heterochiral Centers and Their Application in Asymmetric Aldol Reaction
ACS omega, 2018-07, Vol.3 (7), p.8329-8336
2018
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Aldol–Tishchenko–Tishchenko reaction: sodium tert-butoxide-mediated one step formation of 1,3-glycol diester from benzaldehyde and isobutyrophenone
Mendeleev communications, 2013-03, Vol.23 (2), p.96-97
2013
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Organocatalytic, enantioselective synthesis of benzoxaboroles via Wittig/oxa-Michael reaction Cascade of α-formyl boronic acids
Chemical science (Cambridge), 2017-04, Vol.8 (4), p.3026-3030
2017
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A new organocatalyst derived from abietic acid and 4-hydroxy-l-proline for direct asymmetric aldol reactions in aqueous media
Tetrahedron: asymmetry, 2014-10, Vol.25 (18-19), p.1292-1297
2014
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The smallest organocatalyst in highly enantioselective direct aldol reaction in wet solvent-free conditions
RSC advances, 2014-01, Vol.4 (46), p.24311-24315
2014
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Organocatalytic, enantioselective synthesis of benzoxaboroles via Wittig/oxa-Michael reaction Cascade of α-formyl boronic acidsElectronic supplementary information (ESI) available. CCDC 1487136. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc04522g
2017-03
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Organocatalytic, enantioselective synthesis of benzoxaboroles via Wittig/oxa-Michael reaction Cascade of α-formyl boronic acids† †Electronic supplementary information (ESI) available. CCDC 1487136. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc04522g Click here for additional data file. Click here for additional data file
Chemical science (Cambridge), 2017-01, Vol.8 (4), p.3026-3030
2017
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Corrigendum to “Advances on asymmetric organocatalytic 1,4-conjugate addition reactions in aqueous and semi-aqueous media” [Tetrahedron: Asymmetry 2017, 849–875]
Tetrahedron: asymmetry, 2017-11
2017
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AldolaTishchenkoaTishchenko reaction: sodium tert-butoxide-mediated one step formation of 1,3-glycol diester from benzaldehyde and isobutyrophenone
Mendeleev communications, 2013-04, Vol.23 (2), p.96-97
2013
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The smallest organocatalyst in highly enantioselective direct aldol reaction in wet solvent-free conditionsElectronic supplementary information (ESI) available: Experimental procedure, NMR, spectra, and HPLC traces. See DOI: 10.1039/c4ra02690j
2014-06
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ChemInform Abstract: Water: The Most Versatile and Nature′s Friendly Media in Asymmetric Organocatalyzed Direct Aldol reactions
ChemInform, 2015-12, Vol.46 (52), p.no-no
2015
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ChemInform Abstract: Water: The Most Versatile and Nature's Friendly Media in Asymmetric Organocatalyzed Direct Aldol reactions
ChemInform, 2015-12, Vol.46 (52)
2015
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ChemInform Abstract: Advances on Asymmetric Organocatalyzed Mannich Reactions in Aqueous and Non‐Aqueous Media
ChemInform, 2016-05, Vol.47 (24), p.no-no
2016
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ChemInform Abstract: Aldol-Tishchenko-Tishchenko Reaction: Sodium tert-Butoxide-Mediated One Step Formation of 1,3-Glycol Diester from Benzaldehyde and Isobutyrophenone
ChemInform, 2013-07, Vol.44 (30), p.no-no
2013
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ChemInform Abstract: A New Organocatalyst Derived from Abietic Acid and 4-Hydroxy-L-proline for Direct Asymmetric Aldol Reactions in Aqueous Media
ChemInform, 2015-03, Vol.46 (12), p.no-no
2015
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ChemInform Abstract: The Smallest Organocatalyst in Highly Enantioselective Direct Aldol Reaction in Wet Solvent-Free Conditions
ChemInform, 2015-01, Vol.46 (4), p.no-no
2015
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ChemInform Abstract: Catalytic Asymmetric Carbon-Carbon Bond-Forming Reactions in Aqueous Media
ChemInform, 2012-06, Vol.43 (23), p.no-no
2012
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