Year |
Citation |
Score |
2023 |
Bankar OS, Laha D, Meher KB, Bhat RG. Umpolung Reactivity of Diazo Arylidene Succinimides: Distal C-H Functionalization of α-Thiocarbonyls from the Reactive Carbenoid Center. Chemistry, An Asian Journal. e202300774. PMID 37828837 DOI: 10.1002/asia.202300774 |
0.784 |
|
2023 |
Bhowmick A, Chatterjee A, Pathak SS, Bhat RG. A visible light-driven direct synthesis of industrially relevant glutaric acid diesters from aldehydes. Chemical Communications (Cambridge, England). PMID 37724011 DOI: 10.1039/d3cc02557h |
0.651 |
|
2023 |
Khade VV, Bhowmick A, Thube AS, Bhat RG. Direct Access to Strained Fused Dihalo-Aziridino Quinoxalinones via C3-Alkylation Followed by Tandem Cyclization. The Journal of Organic Chemistry. 88: 8010-8023. PMID 37262098 DOI: 10.1021/acs.joc.3c00033 |
0.801 |
|
2023 |
Dharpure PD, Behera M, Thube AS, Bhat RG. Base Dependent Rearrangement of Dithiane and Dithiolane under Visible-light Photoredox catalysis. Chemistry, An Asian Journal. e202201128. PMID 36630181 DOI: 10.1002/asia.202201128 |
0.802 |
|
2022 |
Navale BS, Laha D, Banerjee S, Vanka K, Bhat RG. Highly Site-Selective Direct C-H Bond Functionalization of Unactivated Arenes with Propargyl α-Aryl-α-diazoacetates via Scandium Catalysis. The Journal of Organic Chemistry. PMID 36181673 DOI: 10.1021/acs.joc.2c01185 |
0.804 |
|
2022 |
Dharpure PD, Behera M, Khade VV, Thube AS, Bhat RG. Direct Access to Thiocyano-Thioesters from Cyclic Thioacetals via Photoredox Catalysis: An Introduction of Two Functional Groups in One Pot. Organic Letters. PMID 36121933 DOI: 10.1021/acs.orglett.2c02601 |
0.776 |
|
2022 |
Khade VV, Thube AS, Dharpure PD, Bhat RG. Direct synthesis of 1,3-dithiolanes from terminal alkynes visible light photoredox catalysis. Organic & Biomolecular Chemistry. PMID 35076051 DOI: 10.1039/d1ob02154k |
0.793 |
|
2021 |
Warghude PK, Sabale AS, Dixit R, Vanka K, Bhat RG. An easy and practical approach to access multifunctional cylcopentadiene- and cyclopentene-spirooxindoles [3 + 2] annulation. Organic & Biomolecular Chemistry. PMID 33908568 DOI: 10.1039/d1ob00514f |
0.793 |
|
2020 |
Reddy C, Shaikh JY, Bhat RG. Access to Hetero-Benzyl Scaffolds via Transient-Ligand-Enabled Direct γ-C(sp3)-H Arylation of 3-Methylheteroarene-2-Carbaldehydes. The Journal of Organic Chemistry. PMID 32348142 DOI: 10.1021/Acs.Joc.0C00154 |
0.84 |
|
2020 |
Warghude PK, Sabale AS, Bhat RG. Access to highly enantioselective and diastereoselective spirooxindole dihydrofuran fused pyrazolones. Organic & Biomolecular Chemistry. PMID 32077889 DOI: 10.1039/D0Ob00007H |
0.819 |
|
2020 |
Dharpure PD, Bhowmick A, Warghude PK, Bhat RG. Visible-light mediated facile dithiane deprotection under metal free conditions Tetrahedron Letters. 61: 151407. DOI: 10.1016/J.Tetlet.2019.151407 |
0.798 |
|
2020 |
Laha D, Bhat RG. Silver‐Catalyzed Epoxidation of Aldehydes Using Donor‐/Acceptor‐type Vinyl Diazosuccinimides to Access Spiro‐Pyrrolidinedioneoxiranes Asian Journal of Organic Chemistry. 9: 918-921. DOI: 10.1002/Ajoc.202000123 |
0.825 |
|
2019 |
Navale BS, Laha D, Bhat RG. Propargyl α-aryl-α-diazoacetates as robust reagents for the effective C-H bond functionalization of 1,3-diketones via scandium catalysis Tetrahedron Letters. 60: 1899-1903. DOI: 10.1016/J.Tetlet.2019.06.026 |
0.809 |
|
2019 |
Khopade TM, Warghude PK, Mete TB, Bhat RG. Acyl/aroyl Meldrum’s acid as an enol surrogate for the direct organocatalytic synthesis of α,β-unsaturated ketones Tetrahedron Letters. 60: 197-200. DOI: 10.1016/J.Tetlet.2018.12.013 |
0.825 |
|
2019 |
Syamala LVB, Khopade TM, Warghude PK, Bhat RG. An access to α, β-unsaturated ketones via dual cooperative catalysis Tetrahedron Letters. 60: 88-91. DOI: 10.1016/J.Tetlet.2018.11.065 |
0.838 |
|
2018 |
Khopade TM, Warghude PK, Sonawane AD, Bhat RG. Multicomponent synthesis of pyroglutamic acid derivatives via Knoevenagel-Michael-hydrolysis-lactamization-decarboxylation (KMHL-D) sequence. Organic & Biomolecular Chemistry. PMID 30574984 DOI: 10.1039/C8Ob02473A |
0.828 |
|
2018 |
Bhat RG, Khopade TM, Mete TB, Arora JS. An Adverse Effect of Higher Catalyst Loading and Longer Reaction Time on Enantioselectivity in Organocatalytic Multicomponent Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29465758 DOI: 10.1002/Chem.201800278 |
0.824 |
|
2018 |
Warghude PK, Dharpure PD, Bhat RG. Cycloaddition of isatin-derived MBH carbonates and 3-methyleneoxindoles to construct diastereoselective cyclopentenyl bis-spirooxindoles and cyclopropyl spirooxindoles: Catalyst controlled [3 + 2] and [2 + 1] annulations Tetrahedron Letters. 59: 4076-4079. DOI: 10.1016/J.Tetlet.2018.10.004 |
0.831 |
|
2018 |
Syamala LVRB, Mete TB, Bhat RG. FeCl3·6H2O-catalyzed selective conjugate reduction of alkylidene-β-keto esters and alkylidene-1,3-diketones Tetrahedron Letters. 59: 3288-3291. DOI: 10.1016/J.Tetlet.2018.07.041 |
0.838 |
|
2018 |
Mete TB, Laha D, Bhat RG. A One Pot Transition‐Metal‐Free Synthesis of Styrenyl Ethers from 2‐Aryloxy/Alkoxy Acetophenones Chemistryselect. 3: 7656-7659. DOI: 10.1002/SLCT.201801522 |
0.831 |
|
2017 |
Syamala LVRB, Bhat RG. FeCl3·6H2O catalyzed diastereoselective synthesis of (L)-menthyl 4-oxo-2-arylpiperidine-3-carboxylates Tetrahedron Letters. 58: 4836-4840. DOI: 10.1016/J.Tetlet.2017.11.026 |
0.527 |
|
2017 |
Mete TB, Singh A, Bhat RG. Transition-Metal-Free Synthesis of Primary to Tertiary Carboxamides: A Quick Access to Prodrug-Pyrazinecarboxamide Tetrahedron Letters. 58: 4709-4712. DOI: 10.1016/J.Tetlet.2017.11.006 |
0.808 |
|
2017 |
Mete TB, Khopade TM, Bhat RG. Oxidative decarboxylation of arylacetic acids in water: One-pot transition-metal-free synthesis of aldehydes and ketones Tetrahedron Letters. 58: 2822-2825. DOI: 10.1016/J.Tetlet.2017.06.013 |
0.803 |
|
2017 |
Mohite AR, Mete TB, Bhat RG. An expedient stereoselective synthesis of (E)-α,β-unsaturated esters and thioesters using FeCl3·6H2O Tetrahedron Letters. 58: 770-774. DOI: 10.1016/J.Tetlet.2017.01.024 |
0.82 |
|
2017 |
Mete TB, Khopade TM, Bhat RG. Transition-metal-free regioselective thiocyanation of phenols, anilines and heterocycles Tetrahedron Letters. 58: 415-418. DOI: 10.1016/J.Tetlet.2016.12.043 |
0.823 |
|
2017 |
Khopade TM, Sonawane AD, Arora JS, Bhat RG. Direct Organocatalytic Multicomponent Synthesis of Enantiopure γ
-Butyrolactones via Tandem Knoevenagel-Michael-Lactonization Sequence Advanced Synthesis & Catalysis. 359: 3905-3910. DOI: 10.1002/Adsc.201701084 |
0.837 |
|
2014 |
Sultane PR, Mete TB, Bhat RG. Chemoselective N-deacetylation under mild conditions. Organic & Biomolecular Chemistry. 12: 261-4. PMID 24281043 DOI: 10.1039/C3Ob41971A |
0.79 |
|
2014 |
Sultane PR, Mete TB, Bhat RG. A convenient protocol for the deprotection of N-benzyloxycarbonyl (Cbz) and benzyl ester groups Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2015.02.131 |
0.805 |
|
2013 |
Mohite AR, Bhat RG. A practical and convenient protocol for the synthesis of (E)-α,β-unsaturated acids. Organic Letters. 15: 4564-7. PMID 23962223 DOI: 10.1021/Ol402130T |
0.838 |
|
2013 |
Navale BS, Bhat RG. Copper(I) iodide–DMAP catalyzed homo- and heterocoupling of terminal alkynes Rsc Advances. 3: 5220-5226. DOI: 10.1039/C3Ra23478A |
0.798 |
|
2012 |
Sultane PR, Bhat RG. Stereoselective approach to cis-2,3-disubstituted piperidines via reduction of N-acyliminium ion intermediate: enantioselective synthesis of (+)-(2S,3S)-CP-99,994. The Journal of Organic Chemistry. 77: 11349-54. PMID 23186126 DOI: 10.1021/Jo302181K |
0.797 |
|
2012 |
Mohite AR, Bhat RG. Enantiopure synthesis of side chain-modified α-amino acids and 5-cis-alkylprolines. The Journal of Organic Chemistry. 77: 5423-8. PMID 22616793 DOI: 10.1021/Jo300653U |
0.819 |
|
2012 |
Sultane PR, Mohite AR, Bhat RG. Total synthesis of 1-deoxy-7,8a-di-epi-castanospermine and formal synthesis of pumiliotoxin-251D Tetrahedron Letters. 53: 5856-5858. DOI: 10.1016/J.Tetlet.2012.08.061 |
0.79 |
|
2012 |
Mohite AR, Sultane PR, Bhat RG. BF3·Et2O and trifluoroacetic acid/triethyl amine-mediated synthesis of functionalized piperidines Tetrahedron Letters. 53: 30-35. DOI: 10.1016/J.Tetlet.2011.10.072 |
0.842 |
|
2012 |
Mohite AR, Sultane PR, Bhat RG. ChemInform Abstract: BF3·Et2O and Trifluoroacetic Acid/Triethyl Amine Mediated Synthesis of Functionalized Piperidines. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201217154 |
0.812 |
|
2008 |
Choubdar N, Bhat RG, Stubbs KA, Yuzwa S, Pinto BM. Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analogue of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against O-GlcNAcase and NagZ enzymes. Carbohydrate Research. 343: 1766-77. PMID 18358456 DOI: 10.1016/J.Carres.2008.02.027 |
0.617 |
|
2007 |
Bhat RG, Kumar NS, Pinto BM. Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol. Carbohydrate Research. 342: 1934-42. PMID 17572396 DOI: 10.1016/J.Carres.2007.05.030 |
0.588 |
|
2007 |
Choudhury AR, Bhat RG, Guru Row TN, Chandrasekaran S. Weak Csp3−H···F−C Interaction Overshadows the Strong C⋮C−H···OC Hydrogen Bond: Structure of Pentafluorophenyl Prop-2-ynyl Carbonate Crystal Growth & Design. 7: 844-846. DOI: 10.1021/Cg060489T |
0.647 |
|
2005 |
Ramesh R, Bhat RG, Chandrasekaran S. Highly selective deblocking of propargyl carbonates in the presence of propargyl carbamates with tetrathiomolybdate. The Journal of Organic Chemistry. 70: 837-40. PMID 15675840 DOI: 10.1021/Jo048777O |
0.723 |
|
2005 |
Bhat RG, Ghosh Y, Chandrasekaran S. A Mild and Selective Method for N-Dealkylation of Tertiary Amines. Cheminform. 36. DOI: 10.1002/CHIN.200505057 |
0.296 |
|
2004 |
Bhat RG, Ghosh Y, Chandrasekaran S. A mild and selective method for N-dealkylation of tertiary amines Tetrahedron Letters. 45: 7983-7985. DOI: 10.1016/J.Tetlet.2004.09.018 |
0.738 |
|
2003 |
Bhat RG, Porhiel E, Saravanan V, Chandrasekaran S. Utility of tetrathiomolybdate and tetraselenotungstate: efficient synthesis of cystine, selenocystine, and their higher homologues Tetrahedron Letters. 44: 5251-5253. DOI: 10.1016/S0040-4039(03)01222-X |
0.746 |
|
2002 |
Bhat RG, Sinha S, Chandrasekaran S. Propargyloxycarbonyl (Poc) amino acid chlorides as efficient coupling reagents for the synthesis of 100% diastereopure peptides and resin bound tetrathiomolybdate as an effective deblocking agent for the Poc group. Chemical Communications (Cambridge, England). 812-3. PMID 12122992 DOI: 10.1039/B200155A |
0.784 |
|
2002 |
Bhat RG, Kérourédan E, Porhiel E, Chandrasekaran S. Synthesis and applications of propargyl pentafluorophenyl carbonate for peptide synthesis Tetrahedron Letters. 43: 2467-2469. DOI: 10.1016/S0040-4039(02)00287-3 |
0.739 |
|
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