| Year |
Citation |
Score |
| 2021 |
Kaur BP, Kaur J, Chimni SS. Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles. Rsc Advances. 11: 2126-2140. PMID 35424187 DOI: 10.1039/d0ra09133b |
0.458 |
|
| 2021 |
Kaur BP, Sharma V, Sahoo SC, Chimni SS. Low catalyst loading enabled organocatalytic synthesis of chiral bis-heterocyclic frameworks containing pyrazole and isoxazole. Organic & Biomolecular Chemistry. 19: 9910-9924. PMID 34734954 DOI: 10.1039/d1ob01313k |
0.509 |
|
| 2021 |
Gautam S, Chimni SS, Arora S, Sohal SK. Toxic effects of purified phenolic compounds from Acacia nilotica against common cutworm. Toxicon : Official Journal of the International Society On Toxinology. 203: 22-29. PMID 34600912 DOI: 10.1016/j.toxicon.2021.09.017 |
0.242 |
|
| 2020 |
Kumar N, Kumar A, Sahoo SC, Chimni SS. Candida antarctica lipase-B-catalyzed kinetic resolution of 1,3-dialkyl-3-hydroxymethyl oxindoles. Chirality. PMID 33141985 DOI: 10.1002/chir.23284 |
0.425 |
|
| 2020 |
Kaur J, Kaur BP, Chimni SS. Recent advances in the catalytic synthesis of 3-aminooxindoles: an update. Organic & Biomolecular Chemistry. PMID 32515465 DOI: 10.1039/D0Ob00777C |
0.492 |
|
| 2019 |
Sharma A, Sharma V, Chimni SS. Organocatalytic enantioselective conjugate addition of pyrazolin-5-ones to arylomethylidene malonates. Organic & Biomolecular Chemistry. PMID 31657819 DOI: 10.1039/C9Ob01700C |
0.576 |
|
| 2019 |
Singh K, Malviya BK, Jaiswal PK, Verma VP, Chimni SS, Sharma S. Phenanthridine-Fused Tetracyclic Ring System: Metal-Free Diastereoselective Modular Construction of Highly Constrained Polyheterocycles via Post-Ugi Tandem Modifications. Organic Letters. PMID 31414822 DOI: 10.1021/Acs.Orglett.9B02340 |
0.502 |
|
| 2019 |
Kaur J, Chimni SS. Catalytic synthesis of 3-aminooxindoles via addition to isatin imine: an update. Organic & Biomolecular Chemistry. 16: 3328-3347. PMID 29664071 DOI: 10.1039/C7Ob03002A |
0.488 |
|
| 2018 |
Sharma V, Kaur A, Sahoo SC, Chimni SS. Enantioselective 1,4-Michael addition reaction of pyrazolin-5-one derivatives with 2-enoylpyridines catalyzed by Cinchona derived squaramides. Organic & Biomolecular Chemistry. PMID 30151544 DOI: 10.1039/C8Ob01588K |
0.586 |
|
| 2018 |
Sharma V, Bhardwaj VK, Chimni SS. Stereoselective Organocatalytic Synthesis of
γ,γ‐
Disubstituted Butenolides Chemistryselect. 3: 5348-5352. DOI: 10.1002/slct.201801217 |
0.413 |
|
| 2018 |
Sharma V, Kaur J, Chimni SS. Chiral Squaramide Catalyzed Enantioselective 1,6-Michael Addition of Pyrazolin-5-ones to Styrylisoxazole Derivatives European Journal of Organic Chemistry. 2018: 3489-3495. DOI: 10.1002/Ejoc.201800589 |
0.548 |
|
| 2018 |
Kumari A, Kaur J, Bhardwaj VK, Chimni SS. Organocatalytic Asymmetric Decarboxylative Addition of β-Ketoacids to Methyleneindolinones Derivatives European Journal of Organic Chemistry. 2018: 4081-4088. DOI: 10.1002/Ejoc.201800454 |
0.411 |
|
| 2017 |
Singh K, Malviya BK, Roy TK, Mithu VS, Bhardwaj VK, Verma VP, Chimni SS, Sharma S. Catalyst-Controlled Structural Divergence: Selective Intramolecular 7-endo-dig and 6-exo-dig Post-Ugi Cyclization for the Synthesis of Benzoxazepinones and Benzoxazinones. The Journal of Organic Chemistry. PMID 29181970 DOI: 10.1021/Acs.Joc.7B02123 |
0.452 |
|
| 2017 |
Kaur J, Chauhan P, Singh S, Chimni SS. Journey Heading Towards Enantioselective Synthesis Assisted by Organocatalysis. Chemical Record (New York, N.Y.). PMID 28851023 DOI: 10.1002/Tcr.201700020 |
0.713 |
|
| 2017 |
Saini P, Kumar N, Wani SI, Sharma S, Chimni SS, Sareen D. Bioresolution of racemic phenyl glycidyl ether by a putative recombinant epoxide hydrolase from Streptomyces griseus NBRC 13350. World Journal of Microbiology & Biotechnology. 33: 82. PMID 28378221 DOI: 10.1007/S11274-017-2248-Z |
0.48 |
|
| 2017 |
Islam N, Chimni SS. Geometrical structure and nonlinear response variations of metal (M = Ni2+, Pd2+, Pt2+) octaphyrin complex derivatives: A DFT study Journal of Coordination Chemistry. 70: 1221-1236. DOI: 10.1080/00958972.2017.1290799 |
0.346 |
|
| 2017 |
Kaur J, Kumari A, Chimni SS. Grinding assisted, column chromatography free decarboxylative carbon-carbon bond formation: Greener synthesis of 3, 3-disubstituted oxindoles Tetrahedron. 73: 802-808. DOI: 10.1016/J.Tet.2016.12.070 |
0.481 |
|
| 2017 |
Islam N, Chimni SS. Binding and selectivity of phenazino-18-crown-6-ether with alkali, alkaline earth and toxic metal species: A DFT study Journal of Molecular Structure. 1130: 781-790. DOI: 10.1016/J.Molstruc.2016.10.100 |
0.327 |
|
| 2017 |
Islam N, Chimni SS. Spectral and optoelectronic studies on 7,12,17-trioxa and 7,12,17-trithia [11] helicenes: a DFT view Indian Journal of Physics. 91: 915-924. DOI: 10.1007/S12648-017-1000-8 |
0.349 |
|
| 2017 |
Kaur J, Islam N, Kumar A, Chimni SS. Experimental and DFT Studies of Organocatalytic Microwave-Assisted Reaction of Isatin Derivatives with Dinitrotoluenes Asian Journal of Organic Chemistry. 6: 575-582. DOI: 10.1002/Ajoc.201600614 |
0.506 |
|
| 2017 |
Kaur J, Kumari A, Bhardwaj VK, Chimni SS. Chiral Squaramide-Catalyzed Enantioselective Decarboxylative Addition of β-Keto Acids to Isatin Imines Advanced Synthesis & Catalysis. 359: 1725-1734. DOI: 10.1002/Adsc.201700011 |
0.571 |
|
| 2016 |
Kaur J, Chauhan P, Chimni SS. α,α-Dicyanoolefins: versatile substrates in organocatalytic asymmetric transformations. Organic & Biomolecular Chemistry. PMID 27405916 DOI: 10.1039/C6Ob01229A |
0.581 |
|
| 2016 |
Chimni SS, Kumar M, Kaur BP. 2,4-DNP Catalyzed α-Csp3-H and Csp1-H Bond Functionalization of Cyclic Amines and Alkyne: Highly Regio-/ Diastereoselective Synthesis of α-Alkynyl-3-Amino-2-Oxindoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27172228 DOI: 10.1002/Chem.201601222 |
0.481 |
|
| 2016 |
Mahajan S, Chauhan P, Kumar A, Chimni SS. Organocatalytic enantioselective synthesis of N-alkyl/aryl-3-alkyl-pyrrolidine-2,5-dione in brine Tetrahedron: Asymmetry. 27: 1145-1152. DOI: 10.1016/J.Tetasy.2016.09.004 |
0.683 |
|
| 2016 |
Kaur J, Islam N, Kumar A, Bhardwaj VK, Chimni SS. Organocatalytic enantioselective synthesis of C3 functionalized indole derivatives Tetrahedron. 72: 8042-8049. DOI: 10.1016/J.Tet.2016.10.037 |
0.529 |
|
| 2016 |
Islam N, Chimni SS. DFT investigation on nonlinear optical (NLO) properties of novel borazine derivatives Computational and Theoretical Chemistry. 1086: 58-66. DOI: 10.1016/J.Comptc.2016.04.016 |
0.367 |
|
| 2016 |
Kumar M, Kaur BP, Chimni SS. ChemInform Abstract: 2,4-Dinitrophenol-Catalyzed α-C(sp3)-H and C(sp)-H Bond Functionalization of Cyclic Amines and Alkynes: Highly Regio-/Diastereoselective Synthesis of α-Alkynyl-3-amino-2-oxindoles. Cheminform. 47. DOI: 10.1002/chin.201649123 |
0.349 |
|
| 2016 |
Kumar N, Kaur J, Kumar A, Islam N, Chimni SS. Catalyst-Free Synthesis of 3-Aryl-3-hydroxy-2-oxindole Derivatives by Using Water as the Solvent: Experimental and DFT Studies Asian Journal of Organic Chemistry. DOI: 10.1002/Ajoc.201600346 |
0.499 |
|
| 2015 |
Kumar A, Sharma V, Kaur J, Kumar N, Chimni SS. Maleimide as an efficient nucleophilic partner in the aza-Morita-Baylis-Hillman reaction: synthesis of chiral 3-substituted-3-aminooxindoles. Organic & Biomolecular Chemistry. 13: 5629-35. PMID 25747756 DOI: 10.1039/C5Ob00182J |
0.594 |
|
| 2015 |
Kumar V, Chimni SS. Recent developments on thiourea based anticancer chemotherapeutics. Anti-Cancer Agents in Medicinal Chemistry. 15: 163-75. PMID 24712324 DOI: 10.2174/1871520614666140407123526 |
0.473 |
|
| 2015 |
Singh S, Chimni SS. Recent Advances in Iodine Monochloride Mediated Electrophilic Cyclizations Synthesis (Germany). 47: 1961-1989. DOI: 10.1055/S-0034-1378705 |
0.613 |
|
| 2015 |
Kaur J, Chimni SS, Mahajan S, Kumar A. Stereoselective synthesis of 3-amino-2-oxindoles from isatin imines: new scaffolds for bioactivity evaluation Rsc Advances. 5: 52481-52496. DOI: 10.1039/C5Ra06969F |
0.525 |
|
| 2015 |
Saini P, Wani SI, Kumar R, Chhabra R, Chimni SS, Sareen D. Corrigendum to "Trigger factor assisted folding of the recombinant epoxide hydrolases identified from C. pelagibacter and S. nassauensis" Protein Expr. Purif. 104 (2014) 71-84 Protein Expression and Purification. DOI: 10.1016/J.Pep.2014.10.011 |
0.344 |
|
| 2015 |
Kumar V, Chimni SS. Recent developments on thiourea based anticancer chemotherapeutics Anti-Cancer Agents in Medicinal Chemistry. 15: 163-175. |
0.233 |
|
| 2014 |
Saini P, Wani SI, Kumar R, Chhabra R, Chimni SS, Sareen D. Trigger factor assisted folding of the recombinant epoxide hydrolases identified from C. pelagibacter and S. nassauensis. Protein Expression and Purification. 104: 71-84. PMID 25229949 DOI: 10.1016/J.Pep.2014.09.004 |
0.439 |
|
| 2014 |
Kumar A, Chimni SS. Primary-tertiary diamine-catalyzed Michael addition of ketones to isatylidenemalononitrile derivatives. Beilstein Journal of Organic Chemistry. 10: 929-35. PMID 24991242 DOI: 10.3762/Bjoc.10.91 |
0.518 |
|
| 2014 |
Kumar A, Kaur J, Chauhan P, Chimni SS. Organocatalytic asymmetric Friedel-Crafts reaction of sesamol with isatins: access to biologically relevant 3-aryl-3-hydroxy-2-oxindoles. Chemistry, An Asian Journal. 9: 1305-10. PMID 24591414 DOI: 10.1002/Asia.201301546 |
0.701 |
|
| 2014 |
Kumar V, Kumar A, Sureshbabu VV, Chimni SS. Synthesis and stereochemistry-activity relationship of chiral thiourea derivatives as potential anticancer agents. Anti-Cancer Agents in Medicinal Chemistry. 14: 910-20. PMID 24164047 DOI: 10.2174/18715206113136660368 |
0.505 |
|
| 2014 |
Kumar A, Chimni SS. Primary-tertiary diamine-catalyzed Michael addition of ketones to isatylidenemalononitrile derivatives Beilstein Journal of Organic Chemistry. 10: 929-935. DOI: 10.3762/bjoc.10.91 |
0.446 |
|
| 2014 |
Kaur J, Kumar A, Chimni SS. Cinchonidine thiourea catalyzed asymmetric addition of phenols to oxindole derivatives Rsc Advances. 4: 62367-62374. DOI: 10.1039/C4Ra09805F |
0.593 |
|
| 2014 |
Kumar A, Kaur J, Chimni SS, Jassal AK. Organocatalytic enantioselective aza-Henry reaction of ketimines derived from isatins: Access to optically active 3-amino-2-oxindoles Rsc Advances. 4: 24816-24819. DOI: 10.1039/C4Ra00902A |
0.572 |
|
| 2014 |
Kaur J, Kumar A, Chimni SS. Organocatalytic asymmetric Friedel-Crafts reaction of 1-naphthols with isatins: An enantioselective synthesis of 3-aryl-3-hydroxy-2-oxindoles Tetrahedron Letters. 55: 2138-2141. DOI: 10.1016/J.Tetlet.2014.02.054 |
0.559 |
|
| 2014 |
Kumar A, Sharma V, Kaur J, Kumar V, Mahajan S, Kumar N, Chimni SS. Cinchona-derived thiourea catalyzed hydrophosphonylation of ketiminesdan enantioselective synthesis of α-amino phosphonates Tetrahedron. 70: 7044-7049. DOI: 10.1016/J.Tet.2014.06.013 |
0.638 |
|
| 2014 |
Kaur J, Kumar A, Chimni SS. ChemInform Abstract: Organocatalytic Asymmetric Friedel-Crafts Reaction of 1-Naphthols with Isatins: An Enantioselective Synthesis of 3-Aryl-3-hydroxy-2-oxindoles. Cheminform. 45: no-no. DOI: 10.1002/chin.201436125 |
0.526 |
|
| 2014 |
Chimni SS, Kumar V, Bala N. Inside Cover: Design of Peptidyl Thiourea Derivatives as Organocatalysts for the Asymmetric Ring Opening ofmeso-Stilbene Oxides (Asian J. Org. Chem. 6/2014) Asian Journal of Organic Chemistry. 3: 654-654. DOI: 10.1002/Ajoc.201490011 |
0.671 |
|
| 2014 |
Chimni SS, Kumar V, Bala N. Design of Peptidyl Thiourea Derivatives as Organocatalysts for the Asymmetric Ring Opening of meso-Stilbene Oxides Asian Journal of Organic Chemistry. 3: 700-705. DOI: 10.1002/Ajoc.201402040 |
0.717 |
|
| 2013 |
Chauhan P, Kaur J, Chimni SS. Asymmetric organocatalytic addition reactions of maleimides: a promising approach towards the synthesis of chiral succinimide derivatives. Chemistry, An Asian Journal. 8: 328-46. PMID 22997193 DOI: 10.1002/Asia.201200684 |
0.696 |
|
| 2013 |
Chauhan P, Chimni SS. Organocatalytic enantioselective aza-Friedel-Crafts reaction of sesamols with N-sulfonylimines catalyzed by 6′-OH Cinchona alkaloids Tetrahedron Letters. 54: 4613-4616. DOI: 10.1016/J.Tetlet.2013.06.032 |
0.672 |
|
| 2013 |
Chauhan P, Chimni SS. Tetrahedron: Asymmetry Report Number 144 Organocatalytic asymmetric synthesis of 3-amino-2-oxindole derivatives bearing a tetra-substituted stereocenter Tetrahedron Asymmetry. 24: 343-356. DOI: 10.1016/J.Tetasy.2013.03.002 |
0.654 |
|
| 2013 |
Kumar A, Chimni SS. Organocatalyzed direct asymmetric aldol reaction of isatins in water: Low catalyst loading in command Tetrahedron. 69: 5197-5204. DOI: 10.1016/J.Tet.2013.04.044 |
0.545 |
|
| 2013 |
Chimni SS, Kaur K, Bala N. Highly enantioselective kinetic resolution of trans-2-(phenylthio) cyclohexanol derivatives by immobilized Candida antartica B lipase Journal of Molecular Catalysis B: Enzymatic. 96: 67-74. DOI: 10.1016/J.Molcatb.2013.06.006 |
0.732 |
|
| 2013 |
Kumar A, Chimni SS. Organocatalytic asymmetric direct aldol reaction of pyruvic aldehyde dimethyl acetal with isatin derivatives European Journal of Organic Chemistry. 4780-4786. DOI: 10.1002/Ejoc.201300411 |
0.595 |
|
| 2013 |
Chauhan P, Chimni SS. ChemInform Abstract: Organocatalytic Asymmetric Synthesis of 3-Amino-2-oxindole Derivatives Bearing a Tetra-Substituted Stereocenter Cheminform. 44: no-no. DOI: 10.1002/chin.201330229 |
0.449 |
|
| 2013 |
Chauhan P, Kaur J, Chimni SS. Asymmetric organocatalytic addition reactions of maleimides: A promising approach towards the synthesis of chiral succinimide derivatives Chemistry - An Asian Journal. 8: 328-346. DOI: 10.1002/asia.201200684 |
0.664 |
|
| 2013 |
Chauhan P, Chimni SS. Inside Cover: Organocatalytic Enantioselective Morita-Baylis-Hillman Reaction of Maleimides with Isatins (Asian J. Org. Chem. 7/2013) Asian Journal of Organic Chemistry. 2: 530-530. DOI: 10.1002/Ajoc.201390019 |
0.654 |
|
| 2013 |
Chauhan P, Chimni SS. Organocatalytic enantioselective morita-baylis-hillman reaction of maleimides with isatins Asian Journal of Organic Chemistry. 2: 586-592. DOI: 10.1002/Ajoc.201300093 |
0.698 |
|
| 2013 |
Chauhan P, Chimni SS. Mechanochemistry-assisted asymmetric organocatalysis: A sustainable approach Sp2. 36-39. |
0.5 |
|
| 2013 |
Singh S, Chimni SS. Pyrrolidine catalyzed diastereoselective direct aldol reaction in water: A green approach Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 52: 1202-1209. |
0.412 |
|
| 2013 |
Chauhan P, Singh S, Chimni SS. D-camphor-10-sulfonic acid: A water compatible organocatalyst for Friedel-Crafts reaction of indoles with electron deficient olefins Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 52: 245-251. |
0.564 |
|
| 2012 |
Chauhan P, Chimni SS. Mechanochemistry assisted asymmetric organocatalysis: A sustainable approach. Beilstein Journal of Organic Chemistry. 8: 2132-41. PMID 23243475 DOI: 10.3762/Bjoc.8.240 |
0.587 |
|
| 2012 |
Bala N, Kaur K, Chimni SS, Saini HS, Kanwar SS. Bioresolution of benzyl glycidyl ether using whole cells of Bacillus alcalophilus. Journal of Basic Microbiology. 52: 383-9. PMID 22052437 DOI: 10.1002/Jobm.201100204 |
0.682 |
|
| 2012 |
Kumar A, Chimni SS. Catalytic asymmetric synthesis of 3-hydroxyoxindole: A potentially bioactive molecule Rsc Advances. 2: 9748-9762. DOI: 10.1039/C2Ra21131A |
0.525 |
|
| 2012 |
Chauhan P, Chimni SS. Recent advances in asymmetric organocatalytic conjugate addition of arenes and hetero-arenes Rsc Advances. 2: 6117-6134. DOI: 10.1039/C2Ra20544K |
0.7 |
|
| 2012 |
Chauhan P, Chimni SS. Aromatic hydroxyl group - A hydrogen bonding activator in bifunctional asymmetric organocatalysis Rsc Advances. 2: 737-758. DOI: 10.1039/C1Ra00872B |
0.593 |
|
| 2012 |
Singh S, Chimni SS. Chiral amine catalyzed enantio- and diastereoselective Michael reaction in brine Tetrahedron Asymmetry. 23: 1068-1079. DOI: 10.1016/J.Tetasy.2012.06.026 |
0.672 |
|
| 2012 |
Chauhan P, Chimni SS. Grinding-Assisted Asymmetric Organocatalysis: A Solvent-free Approach to the Formation of Vicinal Quaternary and Tertiary Stereocenters Asian Journal of Organic Chemistry. 1: 138-141. DOI: 10.1002/Ajoc.201200048 |
0.586 |
|
| 2011 |
Kumar A, Singh S, Kumar V, Chimni SS. Asymmetric syn-selective direct aldol reaction of protected hydroxyacetone catalyzed by primary amino acid derived bifunctional organocatalyst in the presence of water. Organic & Biomolecular Chemistry. 9: 2731-42. PMID 21359299 DOI: 10.1039/C0Ob00898B |
0.742 |
|
| 2011 |
Chauhan P, Chimni SS. Asymmetric organocatalytic aza-Friedel-Crafts reaction of naphthols with N-sulfonyl imines European Journal of Organic Chemistry. 1636-1640. DOI: 10.1002/Ejoc.201001653 |
0.683 |
|
| 2011 |
Chauhan P, Chimni SS. Facile construction of vicinal quaternary and tertiary stereocenters via regio- and stereoselective organocatalytic michael addition to nitrodienes Advanced Synthesis and Catalysis. 353: 3203-3212. DOI: 10.1002/Adsc.201100618 |
0.686 |
|
| 2011 |
Chauhan P, Kaur K, Bala N, Kumar V, Chimni SS. Catalyst-free and solventless Hantzsch ester mediated reduction of nitroolefins at elevated temperature Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 50: 304-309. |
0.682 |
|
| 2010 |
Chauhan P, Chimni SS. Asymmetric addition of indoles to isatins catalysed by bifunctional modified cinchona alkaloid catalysts Chemistry - a European Journal. 16: 7709-7713. PMID 20533467 DOI: 10.1002/Chem.201000846 |
0.605 |
|
| 2010 |
Reddy MV, Thota N, Sangwan PL, Malhotra P, Ali F, Khan IA, Chimni SS, Koul S. Novel bisstyryl derivatives of bakuchiol: targeting oral cavity pathogens. European Journal of Medicinal Chemistry. 45: 3125-34. PMID 20427099 DOI: 10.1016/J.Ejmech.2010.03.049 |
0.404 |
|
| 2010 |
Bala N, Chimni SS. Recent developments in the asymmetric hydrolytic ring opening of epoxides catalysed by microbial epoxide hydrolase Tetrahedron Asymmetry. 21: 2879-2898. DOI: 10.1016/J.Tetasy.2010.11.013 |
0.717 |
|
| 2010 |
Chimni SS, Bala N, Dixit VA, Bharatam PV. Thiourea catalyzed aminolysis of epoxides under solvent free conditions. Electronic control of regioselective ring opening Tetrahedron. 66: 3042-3049. DOI: 10.1016/J.Tet.2010.02.053 |
0.688 |
|
| 2010 |
Bala N, Chimni SS, Saini HS, Chadha BS. Bacillus alcalophilus MTCC10234 catalyzed enantioselective kinetic resolution of aryl glycidyl ethers Journal of Molecular Catalysis B: Enzymatic. 63: 128-134. DOI: 10.1016/J.Molcatb.2009.12.019 |
0.706 |
|
| 2010 |
Kumar S, Kumar V, Singh S, Chimni SS. ChemInform Abstract: A Highly Diastereoselective Synthesis of Homoallylic Alcohol/Amine Appended Uracils: The Role of the Uracil C-4 Carbonyl in Diastereoselectivity Control. Cheminform. 32: no-no. DOI: 10.1002/chin.200141180 |
0.358 |
|
| 2010 |
Singh H, Dolly D, Chimni SS, Kumar S. ChemInform Abstract: Enamine-Induced Ring Transformations of 6-Substituted 5-Formyl-1,3-dimethyluracils. Cheminform. 30: no-no. DOI: 10.1002/chin.199915054 |
0.331 |
|
| 2010 |
SINGH H, DOLLY D, HUNDAL MS, HUNDAL G, SINGH P, CHIMNI SS, KUMAR S. ChemInform Abstract: Acid-Catalyzed Reactions of 5-Formyluracils with Enamines. A Facile Synthesis of 5-Acylvinyluracils. Cheminform. 29: no-no. DOI: 10.1002/chin.199841148 |
0.482 |
|
| 2010 |
SINGH H, DOLLY D, CHIMNI SS, KUMAR S. ChemInform Abstract: Acid-Catalyzed Enamine-Induced Transformations of 1,3-Dimethyl-5- formyluracil. A Unique Annulation Reaction with Enaminones. Cheminform. 27: no-no. DOI: 10.1002/chin.199611195 |
0.431 |
|
| 2010 |
SINGH H, SINGH P, CHIMNI SS, KUMAR S. ChemInform Abstract: Heterocyclic Transformations. Part 6. Studies on the Reactions of 3- Benzyl-6-methyl-1,3-oxazine-2,4(3H)-dione with α-Amino and Hydroxy Amides. Cheminform. 27: no-no. DOI: 10.1002/chin.199602189 |
0.418 |
|
| 2010 |
KUMAR S, CHIMNI SS. ChemInform Abstract: A Facile Reduction of Uracil Derivatives by 1,3-Propanedithiol. Cheminform. 25: no-no. DOI: 10.1002/chin.199428215 |
0.353 |
|
| 2010 |
KUMAR S, CHIMNI SS. ChemInform Abstract: Reactions of Diazines with Nucleophiles. Part 3. Umpolung of Reactivity at the C-5 Position of Uracil. Facile Nucleophilic Reactions of Thiolate Ions at C-5 of 6-Cyano-1,3-dimethyluracil to Procure 5-Alkyl- or 5-Aryl-thio-1,3-dimethyl Cheminform. 23: no-no. DOI: 10.1002/chin.199221202 |
0.411 |
|
| 2010 |
KUMAR S, CHIMNI SS. ChemInform Abstract: Phase-Transfer-Catalyzed Reactions of Thiolate Ions with 5-Bromo-1,3- dimethyluracil. A Reinvestigation of the Mechanism. Cheminform. 23: no-no. DOI: 10.1002/chin.199217199 |
0.341 |
|
| 2009 |
Kumar B, Aga MA, Mukherjee D, Chimni SS, Taneja SC. Allyl tetrahydropyranyl ether: a versatile alcohol/thiol protecting reagent Tetrahedron Letters. 50: 6236-6240. DOI: 10.1016/J.Tetlet.2009.09.026 |
0.474 |
|
| 2009 |
Chimni SS, Singh S, Kumar A. The pH of the reaction controls the stereoselectivity of organocatalyzed direct aldol reactions in water Tetrahedron Asymmetry. 20: 1722-1724. DOI: 10.1016/J.Tetasy.2009.07.014 |
0.613 |
|
| 2009 |
Chimni SS, Singh S, Mahajan D. ChemInform Abstract: Protonated (S)-Prolinamide Derivatives-Water Compatible Organocatalysts for Direct Asymmetric Aldol Reaction. Cheminform. 40. DOI: 10.1002/chin.200916071 |
0.414 |
|
| 2008 |
Gupta P, Taneja SC, Shah BA, Mukherjee D, Parshad R, Chimni SS, Qazi GN. An expedient chemo-enzymatic method for the synthesis of optically active masked 1,2-amino alcohols Tetrahedron Asymmetry. 19: 1898-1903. DOI: 10.1016/J.Tetasy.2008.08.004 |
0.509 |
|
| 2008 |
Kanwar SS, Sharma C, Verma ML, Chauhan S, Chimni SS, Chauhan GS. Short-chain ester synthesis by transesterification employing poly (MAc-co-DMA-cl-MBAm) hydrogel-bound lipase of bacillus coagulons MTCC-6375 Journal of Applied Polymer Science. 109: 1063-1071. DOI: 10.1002/App.25320 |
0.486 |
|
| 2007 |
Rampal P, Saini HS, Raj M, Chimni SS, Chadha BS. Enantiocomplementary reduction of 3-phenylthiopropan-2-one by Bacillus sp.: effect of medium components. Bioresource Technology. 98: 725-8. PMID 16545953 DOI: 10.1016/J.Biortech.2006.02.003 |
0.351 |
|
| 2007 |
Shah BA, Taneja SC, Sethi VK, Gupta P, Andotra SS, Chimni SS, Qazi GN. The formation of novel 1,3-dioxolanes: atypical Baylis-Hillman reaction of a sesquiterpene lactone parthenin Tetrahedron Letters. 48: 955-960. DOI: 10.1016/J.Tetlet.2006.12.019 |
0.526 |
|
| 2007 |
Gupta P, Sethi VK, Taneja SC, Shah BA, Andotra SS, Koul S, Chimni SS, Qazi GN. Odoriferous cyclic ethers via co-halogenation reaction: Facile preparation of nerol oxide, Florol®, Florol® methyl ether, and Pityol® methyl ether Helvetica Chimica Acta. 90: 196-204. DOI: 10.1002/Hlca.200790016 |
0.448 |
|
| 2007 |
Kanwar SS, Kaushal RK, Aggarwal A, Chauhan S, Chimni SS, Chauhan GS. Synthesis of ethyl propionate catalyzed by poly(N-AEAAm-co-AAc)-cl-MBAm hydrogel-immobilized lipase of Bacillus coagulans MTCC-6375 Journal of Applied Polymer Science. 105: 1437-1443. DOI: 10.1002/App.26309 |
0.43 |
|
| 2007 |
Kanwar SS, Verma ML, Maheshwari C, Chauhan S, Chimni SS, Chauhan GS. Properties of poly(AAc-co-HPMA-cl-EGDMA) hydrogel-bound lipase of pseudomonas aeruginosa MTCC-4713 and its use in synthesis of methyl acrylate Journal of Applied Polymer Science. 104: 183-191. DOI: 10.1002/App.25315 |
0.464 |
|
| 2007 |
Mahajan D, Chimni SS. Pyrrolidine catalyzed regioselective and diastereoselective direct aldol reaction in water Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 46: 1355-1358. |
0.427 |
|
| 2007 |
Kanwar SS, Kaushal RK, Verma ML, Kumar Y, Azmi W, Gupta R, Chimni SS, Chauhan GS. Synthesis of ethyl oleate employing synthetic hydrogel-immobilized lipase of Bacillus coagulans MTCC-6375 Indian Journal of Biotechnology. 6: 68-73. |
0.399 |
|
| 2006 |
Kanwar SS, Verma HK, Pathak S, Kaushal RK, Kumar Y, Verma ML, Chimni SS, Chauhan GS. Enhancement of ethyl propionate synthesis by poly (AAc-co-HPMA-cl-MBAm)-immobilized Pseudomonas aeruginosa MTCC-4713, exposed to Hg2+ and NH4+ ions. Acta Microbiologica Et Immunologica Hungarica. 53: 195-207. PMID 16956129 DOI: 10.1556/Amicr.53.2006.2.6 |
0.395 |
|
| 2006 |
Kanwar SS, Kaushal RK, Sultana H, Chimni SS. Purification of a moderate thermotolerant Bacillus coagulans BTS1 lipase and its properties in a hydro-gel system Acta Microbiologica Et Immunologica Hungarica. 53: 77-87. PMID 16696551 DOI: 10.1556/Amicr.53.2006.1.5 |
0.376 |
|
| 2006 |
Kanwar SS, Ghazi IA, Chimni SS, Joshi GK, Rao GV, Kaushal RK, Gupta R, Punj V. Purification and properties of a novel extra-cellular thermotolerant metallolipase of Bacillus coagulans MTCC-6375 isolate Protein Expression and Purification. 46: 421-428. PMID 16290008 DOI: 10.1016/J.Pep.2005.10.007 |
0.369 |
|
| 2006 |
Chimni SS, Mahajan D. Small organic molecule catalyzed enantioselective direct aldol reaction in water Tetrahedron Asymmetry. 17: 2108-2119. DOI: 10.1016/J.Tetasy.2006.07.016 |
0.644 |
|
| 2006 |
Khehra MS, Saini HS, Sharma DK, Chadha BS, Chimni SS. Biodegradation of azo dye C.I. Acid Red 88 by an anoxic - Aerobic sequential bioreactor Dyes and Pigments. 70: 1-7. DOI: 10.1016/J.Dyepig.2004.12.021 |
0.389 |
|
| 2006 |
Kanwar SS, Verma HK, Kaushal RK, Gupta R, Kumar Y, Chimni SS, Chauhan GS. Catalytic potential of a poly(AAc-co-HPMA-cl MBAm)-matrix-immobilized lipase from a thermotolerant Pseudomonas aeruginosa MTCC-4713 Journal of Applied Polymer Science. 100: 4252-4259. DOI: 10.1002/App.24107 |
0.36 |
|
| 2006 |
Kanwar SS, Chauhan GS, Chimni SS, Chauhan S, Rawat GS, Kaushal RK. Methacrylic acid and dodecyl methacrylate (MAc-DMA) hydrogel for enhanced catalytic activity of lipase of Bacillus coagulans MTCC-6375 Journal of Applied Polymer Science. 100: 1420-1426. DOI: 10.1002/App.23462 |
0.416 |
|
| 2006 |
Kanwar SS, Pathak S, Verma HK, Kumar S, Gupta R, Chimni SS, Chauhan GS. Characteristics of poly(AAc5-co-HPMA3-cl-EGDMA 15) hydrogel-immobilized lipase of Pseudomonas aeruginosa MTCC-4713 Journal of Applied Polymer Science. 100: 4636-4644. DOI: 10.1002/App.23129 |
0.376 |
|
| 2006 |
Willbrand M, Sidhwa A, Melosky S, Mao BY, Narendrnath N, Chimni S, Sinha V, Laibinis B, Tajik M. Study of the chamber process kit impact on temperature characterization for hot metal deposition process 2006 Proceedings - 23rd International Vlsi Multilevel Interconnection Conference, Vmic 2006. 321-324. |
0.188 |
|
| 2006 |
Gupta P, Kaushal RK, Chimni SS, Gupta R, Kanwar SS. Purification and biochemical characterization of lipases of thermophilic Pseudomonas aeruginosa BTS-2 Asian Journal of Microbiology, Biotechnology and Environmental Sciences. 8: 361-366. |
0.249 |
|
| 2006 |
Kanwar SS, Gupta M, Gupta R, Kaushal RK, Chimni SS. Properties of hydrogel-entrapped lipase of thermophilic Pseudomonas aeruginosa BTS-2 Indian Journal of Biotechnology. 5: 292-297. |
0.197 |
|
| 2006 |
Kaushal RK, Chimni SS, Kanwar SS. Synthesis of α- and β-naphthyl acetate by alginate-immobilized lipase of Bacillus coagulans MTCC-6375 Minerva Biotecnologica. 18: 31-37. |
0.318 |
|
| 2005 |
Kanwar SS, Kaushal RK, Jawed A, Gupta R, Chimni SS. Methods for inhibition of residual lipase activity in colorimetric assay: A comparative study Indian Journal of Biochemistry and Biophysics. 42: 233-237. PMID 23923547 |
0.278 |
|
| 2005 |
Khehra MS, Saini HS, Sharma DK, Chadha BS, Chimni SS. Comparative studies on potential of consortium and constituent pure bacterial isolates to decolorize azo dyes. Water Research. 39: 5135-41. PMID 16289280 DOI: 10.1016/J.Watres.2005.09.033 |
0.363 |
|
| 2005 |
Chimni SS, Mahajan D, Babu VVS. Protonated chiral prolinamide catalyzed enantioselective direct aldol reaction in water Tetrahedron Letters. 46: 5617-5619. DOI: 10.1016/J.Tetlet.2005.06.112 |
0.672 |
|
| 2005 |
Kapoor M, Anand N, Ahmad K, Koul S, Chimni SS, Taneja SC, Qazi GN. Synthesis of β-adrenergic blockers (R)-(-)-nifenalol and (S)-(+)-sotalol via a highly efficient resolution of a bromohydrin precursor Tetrahedron Asymmetry. 16: 717-725. DOI: 10.1016/J.Tetasy.2004.12.016 |
0.621 |
|
| 2005 |
Chimni SS, Mahajan D. Electron deficiency of aldehydes controls the pyrrolidine catalyzed direct cross-aldol reaction of aromatic/heterocyclic aldehydes and ketones in water Tetrahedron. 61: 5019-5025. DOI: 10.1016/J.Tet.2005.03.045 |
0.678 |
|
| 2005 |
Khehra MS, Saini HS, Sharma DK, Chadha BS, Chimni SS. Decolorization of various azo dyes by bacterial consortium Dyes and Pigments. 67: 55-61. DOI: 10.1016/J.Dyepig.2004.10.008 |
0.375 |
|
| 2005 |
Kanwar SS, Verma HK, Kaushal RK, Gupta R, Chimni SS, Kumar Y, Chauhan GS. Effect of solvents and kinetic parameters on synthesis of ethyl propionate catalysed by poly (AAc-co-HPMA-cl-MBAm)-matrix-immobilized lipase of Pseudomonas aeruginosa BTS-2 World Journal of Microbiology and Biotechnology. 21: 1037-1044. DOI: 10.1007/S11274-004-7869-3 |
0.428 |
|
| 2005 |
Sidhwa A, Willbrand M, Melosky S, Spinner C, Chimni S, Sinha V, Zamudio G, Narendrnath N, Bedi S. A study of the embedded thermo-couples and manufacturing capabilities of a high temperature high uniformity (HTHU) heater used for the metal deposition process 2005 Proceedings - 22nd International Vlsi Multilevel Interconnection Conference, Vmic 2005. 607-612. |
0.212 |
|
| 2005 |
Kanwar SS, Kaushal RK, Verma ML, Kumar Y, Chauhan GS, Gupta R, Chimni SS. Synthesis of ethyl laurate by hydrogel immobilized lipase of Bacillus coagulans MTCC-6375 Indian Journal of Microbiology. 45: 187-193. |
0.381 |
|
| 2004 |
Kanwar SS, Srivastava M, Chimni SS, Ghazi IA, Kaushal RK, Joshi GK. Properties of an immobilized lipase of Bacillus coagulans BTS-1 Acta Microbiologica Et Immunologica Hungarica. 51: 57-73. PMID 15362288 DOI: 10.1556/Amicr.51.2004.1-2.4 |
0.396 |
|
| 2004 |
Sharma DK, Saini HS, Singh M, Chimni SS, Chadha BS. Biological treatment of textile dye acid violet-17 by bacterial consortium in an up-flow immobilized cell bioreactor. Letters in Applied Microbiology. 38: 345-50. PMID 15059201 DOI: 10.1111/J.1472-765X.2004.01500.X |
0.347 |
|
| 2004 |
Sharma DK, Saini HS, Singh M, Chimni SS, Chadha BS. Biodegradation of acid blue-15, a textile dye, by an up-flow immobilized cell bioreactor. Journal of Industrial Microbiology & Biotechnology. 31: 109-14. PMID 15024610 DOI: 10.1007/S10295-004-0121-1 |
0.353 |
|
| 2004 |
Sharma DK, Saini HS, Singh M, Chimni SS, Chadha BS. Isolation and characterization of microorganisms capable of decolorizing various triphenylmethane dyes. Journal of Basic Microbiology. 44: 59-65. PMID 14768029 DOI: 10.1002/Jobm.200310334 |
0.357 |
|
| 2004 |
Sharma DK, Saini HS, Singh M, Chimni SS, Chadha BS. Biotreatment of simulated textile dye effluent containing malachite green by an up-flow immobilized cell bioreactor World Journal of Microbiology and Biotechnology. 20: 431-434. DOI: 10.1023/B:Wibi.0000033073.28111.67 |
0.361 |
|
| 2004 |
Kumar V, Chimni SS, Kumar S. A simple one-step protocol for the olefination of vinylogous formamides Tetrahedron Letters. 45: 3409-3412. DOI: 10.1016/J.Tetlet.2004.03.021 |
0.498 |
|
| 2004 |
Kanwar SS, Kaushal RK, Jawed A, Chimni SS, Punj V. Pretreatment of lipase from Bacillus coagulans BTS-1 with proteases enhances its activity Asian Journal of Microbiology, Biotechnology and Environmental Sciences. 6: 215-219. |
0.219 |
|
| 2003 |
Kapoor M, Anand N, Koul S, Chimni SS, Manhas KS, Raina C, Parshad R, Taneja SC, Qazi GN. Kinetic resolution of 1-chloro-3-(1-naphthyloxy)-2-propanol, an intermediate in the synthesis of β-adrenergic receptor blockers Bioorganic Chemistry. 31: 259-269. PMID 12818235 DOI: 10.1016/S0045-2068(03)00050-6 |
0.654 |
|
| 2003 |
Kumar S, Kumar V, Chimni SS. Novel indium-mediated ternary reactions between indole-3-carboxaldehydes-allyl bromide-enamines: Facile synthesis of bisindolyl- and indolyl-heterocyclic alkanes Tetrahedron Letters. 44: 2101-2104. DOI: 10.1016/S0040-4039(03)00168-0 |
0.581 |
|
| 2002 |
Singh S, Kumar S, Chimni SS. Kinetic resolution of beta- and gamma-hydroxy sulfides by fungal lipase from Humicola lanuginosa. Enantiomer. 7: 231-40. PMID 12206504 DOI: 10.1080/10242430212883 |
0.648 |
|
| 2002 |
Singh S, Kumar S, Chimni SS. First chemoenzymatic synthesis of optically active uracil and chromen-4-one substituted homoallylic alcohols: An entry into chiral pool Synlett. 1277-1280. DOI: 10.1055/S-2002-32966 |
0.581 |
|
| 2002 |
Kumar S, Kaur P, Chimni SS. The efficient allylations of 2-oxocarboxylic acids. Synthesis of 2-allyl derivatives of 2-hydroxycarboxylic acids Synlett. 573-574. DOI: 10.1055/S-2002-22710 |
0.516 |
|
| 2002 |
Singh S, Kumar S, Chimni SS. Chemoenzymatic synthesis of optically active heterocyclic homoallylic and homopropargylic alcohols Tetrahedron Asymmetry. 13: 2679-2687. DOI: 10.1016/S0957-4166(02)00743-7 |
0.681 |
|
| 2002 |
Chimni SS, Singh S, Kumar S, Mahajan S. Kinetic resolution of heteroaryl β-hydroxy sulfides catalyzed by Humicola lanuginosa lipase Tetrahedron Asymmetry. 13: 511-517. DOI: 10.1016/S0957-4166(02)00148-9 |
0.67 |
|
| 2002 |
Kumar S, Kumar V, Chimni SS. Novel indium-mediated deoxygenative α,α-diallylation of indole- and pyrrole-3-carboxaldehydes Tetrahedron Letters. 43: 8029-8031. DOI: 10.1016/S0040-4039(02)01973-1 |
0.449 |
|
| 2001 |
Kumar S, Kaur P, Chimni SS, Singh P. Diastereoselective synthesis of 1-allyl and 1,2-bis(allyl)-1,2- diols: Versatile synthons for substituted tetrahydrofuran derivatives Synlett. 1431-1433. DOI: 10.1055/S-2001-16774 |
0.542 |
|
| 2001 |
Singh S, Kumar S, Chimni SS. Humicola lanuginosa lipase-catalyzed enantioselective resolution of β-hydroxy sulfides: Versatile synthons for enantiopure β-hydroxy sulfoxides Tetrahedron Asymmetry. 12: 2457-2462. DOI: 10.1016/S0957-4166(01)00434-7 |
0.645 |
|
| 2000 |
Kumar S, Kumar V, Chimni SS. Indium-mediated barbier allylations of hydroxyanthraquinones: An expedient synthesis of novel 10-alkenyl-10-hydroxy-9(10H)-anthracenones Journal of Chemical Research - Part S. 314-315. DOI: 10.3184/030823400103167660 |
0.528 |
|
| 2000 |
Singh S, Kumar S, Chimni SS. Enantioselective resolution of 3-phenylthio-2-propanol with Humicola lanuginosa lipase Biotechnology Letters. 22: 1237-1241. DOI: 10.1023/A:1005609332450 |
0.63 |
|
| 2000 |
Kumar S, Kumar V, Chimni SS. ChemInform Abstract: Indium-Mediated Barbier Allylations of Hydroxyanthraquinones: An Expedient Synthesis of Novel 10-Alkenyl-10-hydroxy-9(10H)-anthracenones. Cheminform. 31: no-no. DOI: 10.1002/chin.200050109 |
0.379 |
|
| 1998 |
Singh H, Dolly, Chimni SS, Kumar S. Facile Synthesis of 5-(Substituted vinyl)-uracil Derivatives through Knoevenagel and Stobbe type Condensations of 5-Formyluracils Journal of Chemical Research - Part S. 544-545. DOI: 10.1039/A802515K |
0.485 |
|
| 1998 |
Singh H, Dolly, Chimni SS, Kumar S. Enamine-induced Ring Transformations of 6-Substituted 5-Formyl-1,3-dimethyluracils† Journal of Chemical Research-S. 352-353. DOI: 10.1039/A708683K |
0.434 |
|
| 1998 |
Chimni SS, Singh RJ. Bioreduction of a carbon-nitrogen double bond using immobilized baker's yeast - A first report World Journal of Microbiology and Biotechnology. 14: 247-250. DOI: 10.1023/A:1008894416058 |
0.395 |
|
| 1998 |
Singh H, Dolly, Hundal MS, Hundal G, Singh P, Chimni SS, Kumar S. Acid catalysed reactions of 5-formyluracils with enamines. A facile synthesis of 5-acylvinyluracils Tetrahedron. 54: 7563-7572. DOI: 10.1016/S0040-4020(98)00390-1 |
0.538 |
|
| 1996 |
Singh H, Dolly, Chimni SS, Singh P, Kumar S. A facile single pot synthesis of 5-vinyl-1,3-dimethyluracil from 5-formyl-1,3-dimethyluracil Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 35: 1123-1124. |
0.388 |
|
| 1996 |
Singh H, Singh P, Chimni SS, Kumar S. Variable reactivity pattern of 6-cyano-1, 3-dimethyluracil in PTC reactions with carbanions Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 35: 359-362. |
0.335 |
|
| 1995 |
Kumar S, Chimni SS, Cannoo D, Arora JS. Reactions of diazines with nucleophiles--IV. The reactivity of 5-bromo-1,3,6-trimethyluracil with thiolate ions--substitution versus X-philic versus single electron transfer reactions. Bioorganic & Medicinal Chemistry. 3: 891-7. PMID 7582965 DOI: 10.1016/0968-0896(95)00085-U |
0.456 |
|
| 1995 |
Singh H, Singh P, Chimni SS, Kumar S. Heterocyclic transformations. Part 7. Unprecedented transformations of 1,3-dialkyl-5-formyluracils to 1,3-dialkyl-7-hydroxyquinazolines Journal of the Chemical Society, Perkin Transactions 1. 2363-2367. DOI: 10.1039/P19950002363 |
0.524 |
|
| 1992 |
Kumaar S, Chimni SS, Cannoo D. Phase transfer catalysed oxidative arylthiolation of 1,3,6-trimethyluracil and its 5-bromo derivative Heterocycles. 34: 425-428. DOI: 10.3987/Com-91-5869 |
0.451 |
|
| 1992 |
Kumar S, Chimni SS. Umpolung of reactivity at the c-5 position of uracil:1,2 Facile nucleophilic reactions of thiolate ions at C-5 of 6-cyano-1,3-dimethyluracil to procure 5-alkyl or 5-aryl-thio-1,3-dimethyluracils Journal of the Chemical Society, Perkin Transactions 1. 449-451. DOI: 10.1039/P19920000449 |
0.46 |
|
| 1991 |
Kumar S, Chimni SS, Singh H. Heterocyclic transformations. Part 3. Thiolate ion-induced transformations of 6-methyl-1,3-oxazine-2,4(3H)-diones to 3-(alkyl/arylthio)but-2-enamides Journal of the Chemical Society, Perkin Transactions 1. 1391-1395. DOI: 10.1039/P19910001391 |
0.449 |
|
| 1989 |
SINGH H, CHIMNI SS, KUMAR S. ChemInform Abstract: Heterocyclic Transformations. Part 2. A Facile Synthesis of 3-Alkylthiobuten-2-amide Derivatives. Cheminform. 20. DOI: 10.1002/chin.198942096 |
0.388 |
|
| 1989 |
Kumar S, Chimni SS. Reactions of diazenes with nucleophiles: Part II- Facile one step conversion of 5-bromo-1,3-dimethyluracil to 5-alkyl/aryl-thio-and 6-alkylthio-1,3-dimethyluracil derivatives Indian Journal of Chemistry - Section B Organic Chemistry Including Medicinal Chemistry. 28: 1079-1081. |
0.459 |
|
| 1988 |
Kumar S, Chimni SS. 'Umpolung' of reactivity at C-5 position of uracil: An unprecedented nucleophilic reaction of thiolate ion at C-5 of 6-cyano-1,3-dimethyluracil Heterocycles. 27: 2523-2526. DOI: 10.3987/Com-88-4672 |
0.404 |
|
| 1988 |
SINGH P, CHIMNI SS, SINGH H. ChemInform Abstract: Reactions of Carbenes with Heterocycles. Part 2. Reactions of 1,2,3,4-Tetrahydrocarbazole with Di- and Monochlorocarbenes Under Phase-Transfer Catalytic Conditions. Cheminform. 19. DOI: 10.1002/chin.198844158 |
0.412 |
|
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