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Kishor Chandra Bharadwaj
Kishor Chandra Bharadwaj
在 bhu.ac.in 的电子邮件经过验证
标题
引用次数
引用次数
年份
Intramolecular Morita–Baylis–Hillman and Rauhut–Currier reactions. A catalytic and atom economic route for carbocycles and heterocycles
KC Bharadwaj
RSC advances 5 (93), 75923-75946, 2015
1302015
Synthesis of polyhydroxy piperidines and their analogues: a novel approach towards selective inhibitors of α-glucosidase
G Pandey, KC Bharadwaj, MI Khan, KS Shashidhara, VG Puranik
Organic & biomolecular chemistry 6 (14), 2587-2595, 2008
442008
Pd catalyzed facile synthesis of cyclopenta [b] quinolin-1-one via sequential Sonogashira coupling and annulation. An unusual mode of ring closure, using sulphur as a soft …
RM Singh, R Kumar, KC Bharadwaj, T Gupta
Organic Chemistry Frontiers 3 (9), 1100-1104, 2016
292016
Ligand-free palladium-catalyzed facile construction of tetra cyclic dibenzo [b, h][1, 6] naphthyridine derivatives: domino sequence of intramolecular C–H bond arylation and …
JB Singh, KC Bharadwaj, T Gupta, RM Singh
RSC advances 6 (32), 26993-26999, 2016
252016
Less reactive ketones as electrophiles and acrylamides as activated alkenes in intramolecular Baylis–Hillman reaction: facile synthesis of functionalized γ-lactam frameworks
D Basavaiah, GC Reddy, KC Bharadwaj
Tetrahedron 70 (43), 7991-7995, 2014
252014
Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives
RM Singh, KC Bharadwaj, DK Tiwari
Beilstein Journal of Organic Chemistry 10 (1), 2975-2980, 2014
222014
Alkaloid group of Cinchona officinalis: structural, synthetic, and medicinal aspects
KC Bharadwaj, T Gupta, RM Singh
Synthesis of Medicinal Agents from Plants, 205-227, 2018
202018
The Baylis–Hillman acetates as a source of ambiphilic molecules: a simple synthesis of 1, 3-thiazinane-2-thione frameworks
D Basavaiah, S Pal, G Veeraraghavaiah, KC Bharadwaj
Tetrahedron 71 (28), 4659-4664, 2015
202015
The Acrylamide Moiety as an Activated Alkene Component in the Intramolecular Baylis–Hillman Reaction: Facile Synthesis of Functionalized α‐Methylene Lactam and Spirolactam …
D Basavaiah, GC Reddy, KC Bharadwaj
European Journal of Organic Chemistry 2014 (6), 1157-1162, 2014
182014
Na 2 S-mediated synthesis of terminal alkynes from gem-dibromoalkenes
RM Singh, D Nandini, KC Bharadwaj, T Gupta, RP Singh
Organic & Biomolecular Chemistry 15 (47), 9979-9982, 2017
172017
Chemoselective and Highly Rate Accelerated Intramolecular Aza-Morita–Baylis–Hillman Reaction
KC Bharadwaj
The Journal of Organic Chemistry 83 (23), 14498-14506, 2018
162018
Divergent total synthesis of 1, 6, 8a-tri-epi-castanospermine and 1-deoxy-6, 8a-di-epi-castanospermine from substituted azetidin-2-one (β-lactam), involving a cascade sequence …
DK Tiwari, KC Bharadwaj, VG Puranik, DK Tiwari
Organic & Biomolecular Chemistry 12 (37), 7389-7396, 2014
142014
Acrylamide in Rauhut-Currier reaction; intramolecular isomerization of activated alkenes for quinolone synthesis
KC Bharadwaj
Tetrahedron 73 (38), 5690-5699, 2017
132017
Acryl activation by intramolecular hydrogen bond: Morita Baylis Hillman reaction of acrylamide with broad substrate scope
KC Bharadwaj
ChemistrySelect 2 (19), 5384-5389, 2017
132017
Double Morita–Baylis–Hillman (MBH) strategy; an intermolecular and a chemo selective intramolecular MBH reactions for 5/6 substituted, functionalized piperidine unit
KC Bharadwaj, DK Tiwari
Tetrahedron 72 (2), 312-317, 2016
122016
Cascade SN2′–SNAr, Elimination, and 1,5‐Hydride Shift Reactions by Acetylacetone/Acetoacetic Esters: Synthesis of 9,10‐Dihydroacridines
T Gupta, KC Bharadwaj, RM Singh
European Journal of Organic Chemistry 2016 (29), 4981-4984, 2016
102016
RSC Adv. 2015, 5, 75923–75946; b) P. Xie, Y. Huang
KC Bharadwaj
Org. Biomol. Chem 13, 8578-8595, 2015
102015
Synthesis of Medicinal Agents from plants
KC Bharadwaj, T Gupta, RM Singh
Elsevier, 2018
62018
Catalytic trifluoromethylation of aldehyde and potential application for pyrano [4, 3-b] quionline synthesis
K Mishra, KC Bharadwaj, RM Singh
Tetrahedron Letters 59 (37), 3439-3442, 2018
52018
RSC Adv., 2015, 5, 75923;(h) Y. Wei and M. Shi
KC Bharadwaj
Chem. Rev 113, 6659, 2013
52013
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