| Year |
Citation |
Score |
| 2018 |
Gullapalli S, Roychowdhury A, Khaladkar T, Sawargave S, Janrao R, Kalhapure V, Urunkar G, Kulathingal J, Lekkala RR, Bhadra S, Singh PK, Putta KA, Manwatkar S, Surve P, Gurjar MK. Abstract 1701: EPL-1410, a novel fused heterocycle based orally active dual inhibitor of IDO1/TDO2, as a potential immune-oncology therapeutic Cancer Research. 78: 1701-1701. DOI: 10.1158/1538-7445.Am2018-1701 |
0.335 |
|
| 2014 |
Pramanik C, Bapat K, Chaudhari A, Kulkarni MG, Kolla R, Sompalli S, Tripathy NK, Gurjar MK. An efficient, scalable process for benzphetamine hydrochloride Organic Process Research and Development. 18: 495-500. DOI: 10.1021/Op400313Y |
0.356 |
|
| 2014 |
Pramanik C, Kotharkar S, Patil P, Gotrane D, More Y, Borhade A, Chaugule B, Khaladkar T, Neelakandan K, Chaudhari A, Kulkarni MG, Tripathy NK, Gurjar MK. Commercial manufacturing of propofol: Simplifying the isolation process and control on related substances Organic Process Research and Development. 18: 152-156. DOI: 10.1021/Op400300T |
0.399 |
|
| 2013 |
Pramanik C, Patil P, Kotharkar S, Tripathy NK, Gurjar MK. A new route to cevimeline Tetrahedron Letters. 54: 3043-3045. DOI: 10.1016/J.Tetlet.2013.03.090 |
0.457 |
|
| 2012 |
Pal R, Rahaman H, Gurjar MK. A Carbohydrate Based Total Synthesis of Xestodecalactone B and C: Revision of the Absolute Configuration Current Organic Chemistry. 16: 1159-1168. DOI: 10.2174/138527212800564321 |
0.456 |
|
| 2012 |
Pramanik C, Bapat K, Chaudhari A, Tripathy NK, Gurjar MK. A New Solvent System (Cyclopentyl Methyl Ether–Water) in Process Development of Darifenacin HBr Organic Process Research & Development. 16: 1591-1597. DOI: 10.1021/Op300119S |
0.353 |
|
| 2012 |
Patil GD, Kshirsagar SW, Shinde SB, Patil PS, Deshpande MS, Chaudhari AT, Sonawane SP, Maikap GC, Gurjar MK. Identification, synthesis, and strategy for minimization of potential impurities observed in raltegravir potassium drug substance Organic Process Research and Development. 16: 1422-1429. DOI: 10.1021/Op300077M |
0.424 |
|
| 2012 |
Kshirsagar SW, Deshpande MS, Sonawane SP, Maikap GC, Gurjar MK. Simple Modification To Obtain High Quality Fludarabine Organic Process Research & Development. 16: 840-842. DOI: 10.1021/Op3000509 |
0.393 |
|
| 2012 |
Pramanik C, Hivarekar RR, Deshmukh SS, Tripathy NK, Kotharkar S, Chaudhari A, Gurjar MK. Process development of citalopram/Escitalopram oxalate: Isolation and synthesis of novel impurities Organic Process Research and Development. 16: 824-829. DOI: 10.1021/Op300039C |
0.444 |
|
| 2012 |
Mahale RD, Chaskar SP, Patil KE, Maikap GC, Gurjar MK. Corey–Itsuno Reduction of Ketones: A Development of Safe and Inexpensive Process for Synthesis of Some API Intermediates Organic Process Research & Development. 16: 710-713. DOI: 10.1021/Op300034U |
0.437 |
|
| 2012 |
Pramanik C, Bhumkar R, Karhade G, Khairnar P, Tripathy NK, Gurjar MK. Efficient Synthesis of Impurity-C of Antimigraine Agent Rizatriptan Benzoate Organic Process Research & Development. 16: 507-511. DOI: 10.1021/Op200284M |
0.432 |
|
| 2012 |
Chopade AU, Chopade MU, Chanda BM, Sawaikar DD, Sonawane KB, Gurjar MK. A synthesis of (±)-thia-calanolide A, its resolution and in vitro biological evaluation Arabian Journal of Chemistry. DOI: 10.1016/J.Arabjc.2012.04.027 |
0.417 |
|
| 2012 |
Gurjar MK, Yellol GS, Mohapatra DK. A Carbohydrate-Based Synthesis of the C13-C22 Fragment of Amphidinolide X European Journal of Organic Chemistry. 2012: 1753-1758. DOI: 10.1002/EJOC.201101605 |
0.315 |
|
| 2011 |
Sonawane SP, Patil GD, Gurjar MK. Concise Synthesis of Two β-Adrenergic Blocking Agents in High Stereoselectivity Using the Readily Available Chiral Building Block (2S,2′S,2″S)-Tris-(2,3-epoxypropyl)-isocyanurate Organic Process Research & Development. 15: 1365-1370. DOI: 10.1021/Op2001518 |
0.492 |
|
| 2011 |
Yellol GS, Mohapatra DK, Gurjar MK, Sun C. ChemInform Abstract: Simple and Efficient One Pot Synthetic Protocol to Construct Morpholin-2-ones. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201119155 |
0.337 |
|
| 2011 |
Pal R, Rahaman H, Mohapatra DK, Gurjar MK. ChemInform Abstract: Synthetic Studies of Superstolide A: A Carbohydrate Based Synthesis of the C21-C26 Segment. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201117197 |
0.354 |
|
| 2010 |
Mohapatra DK, Pal R, Rahaman H, Gurjar MK. Stereoselective Formal Total Synthesis Of Novel Antibiotic (-)-Centrolobine Heterocycles. 80: 219-227. DOI: 10.3987/Com-08-S(S)1 |
0.726 |
|
| 2010 |
Pal R, Rahaman H, Mohapatra DK, Gurjar MK. Synthetic Studies of Superstolide A: A Carbohydrate Based Synthesis of the C21-C26 Segment Letters in Organic Chemistry. 7: 657-660. DOI: 10.2174/157017810793811704 |
0.618 |
|
| 2010 |
Joshi S, Maikap GC, Titirmare S, Chaudhari A, Gurjar MK. An Improved Synthesis of Etravirine Organic Process Research & Development. 14: 657-660. DOI: 10.1021/Op9003289 |
0.464 |
|
| 2010 |
Gotrane DM, Deshmukh RD, Ranade PV, Sonawane SP, Bhawal BM, Gharpure MM, Gurjar MK. A novel method for resolution of amlodipine Organic Process Research and Development. 14: 640-643. DOI: 10.1021/Op900283Z |
0.433 |
|
| 2010 |
Chavan AB, Gundecha SS, Kadam PN, Maikap GC, Gurjar MK. Dexmethylphenidate: An efficient process for the racemization of Unwanted (2 S,2 S or l - Threo)-α-Phenyl-α-(2-piperidyl)acetamide Organic Process Research and Development. 14: 1473-1475. DOI: 10.1021/Op100197G |
0.474 |
|
| 2010 |
Mahale RD, Rajput MR, Maikap GC, Gurjar MK. Davis Oxaziridine-Mediated Asymmetric Synthesis of Proton Pump Inhibitors Using DBU Salt of Prochiral Sulfide Organic Process Research & Development. 14: 1264-1268. DOI: 10.1021/Op100075V |
0.472 |
|
| 2010 |
Gurjar MK, Hotha S, Murugaiah AMS. ChemInform Abstract: Role of Asymmetric Catalysts in Chiral Drug Synthesis Cheminform. 33: no-no. DOI: 10.1002/chin.200244259 |
0.646 |
|
| 2010 |
Gurjar MK, Karmakar S, Mohapatra DK, Phalgune UD. ChemInform Abstract: A Novel Application of a [3 + 2] Cycloaddition Reaction for the Synthesis of the Piperazinone Rings of Pseudotheonamides A1 and A2. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200227195 |
0.327 |
|
| 2010 |
Gurjar MK, Maheshwar K. ChemInform Abstract: Stereoselective Synthesis of a Novel Carbocyclic Nucleoside. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200215205 |
0.492 |
|
| 2010 |
Gurjar MK, Reddy R. ChemInform Abstract: Unusual Formation of 2-Butyl-5-alkyloxymethylfuran. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200203119 |
0.299 |
|
| 2010 |
Gurjar MK, Reddy LK, Hotha S. ChemInform Abstract: Synthesis of Oligosaccharides of Motifs D and E of Arabinogalactan Present in Mycobacterium tuberculosis. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200141229 |
0.646 |
|
| 2010 |
Gurjar MK, Ravindranadh SV, Kumar P. ChemInform Abstract: 5-exo-dig, 5-exo-trig Cascade Radical Cyclization on Sugar-Furanose Templates: Entry to Angularly Fused Oxa- and Dioxa-triquinane Skeletons. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200136109 |
0.338 |
|
| 2010 |
Gurjar MK, Krishna LM, Reddy BS, Chorghade MS. ChemInform Abstract: A Versatile Approach to anti-Asthmatic Compound CMI-977 and Its Six-Membered Analogue. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200031116 |
0.289 |
|
| 2010 |
Gurjar MK, Bhaket P. ChemInform Abstract: Total Synthesis of a Novel Cytotoxic Metabolite Gymnastatin A. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200016255 |
0.444 |
|
| 2010 |
Gurjar MK, Pal S, Mohapatra DK. ChemInform Abstract: A New Stereoselective Synthetic Strategy for β-Hydroxy-α-amino Acids of Vancomycin. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199924242 |
0.361 |
|
| 2010 |
MEREYALA HB, HOTHA S, GURJAR MK. ChemInform Abstract: Synthesis of Pentaarabinofuranosyl Structure Motif A of Mycobacterium tuberculosis. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199830236 |
0.638 |
|
| 2010 |
RAO AVR, GURJAR MK, LAKSHMIPATHI P, REDDY MM, NAGARAJAN M, PAL S, SARMA BVNBS, TRIPATHY NK. ChemInform Abstract: SNAr Macrocyclization: A New Approach Towards the Synthesis of D-O-E-Segment of Vancomycin. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199805230 |
0.374 |
|
| 2010 |
BOSE DS, SRINIVAS P, GURJAR MK. ChemInform Abstract: Stereospecific Synthesis of a Novel Azetido(2,1-c)(1,4)benzodiazepine ( ABD) Ring System with DNA Recognition Potential. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199746171 |
0.379 |
|
| 2010 |
GURJAR MK, SARMA BVNBS, RAO AVR. ChemInform Abstract: Enantioselective Epoxidation of 2,2-Dialkyl-2H-chromenes with OxoneR and Jacobsen′s (S,S)-Mn(III)(Ph-Salen)Cl Complex: Solvent Effect. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199735112 |
0.239 |
|
| 2010 |
RAO BV, KRISHNA UM, GURJAR MK. ChemInform Abstract: Stereoselective Synthesis of (2S,3R)-β-Hydroxyornithine. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199732168 |
0.387 |
|
| 2010 |
GURJAR MK, TRIPATHY S. ChemInform Abstract: Synthesis of a Unique Tripeptide L-Glu-Gly-4-hydroxystyrylamine. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199713167 |
0.359 |
|
| 2010 |
GURJAR MK, MAINKAR AS, SRINIVAS P. ChemInform Abstract: Stereoselective Synthesis of the C3-C9 Segment of Soraphen A. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199548255 |
0.357 |
|
| 2010 |
RAO AVR, GURJAR MK, PAL S, PARIZA RJ, CHORGHADE MS. ChemInform Abstract: Synthesis of a Novel C2-Symmetrical (2S,5S)-2,5-Bis-((1,1- dimethylethoxy)carbonylamino)-1,6-diphenylhex-3-ene: Applications in the Synthesis of Potential HIV Protease Inhibitors. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199531109 |
0.384 |
|
| 2010 |
GURJAR MK, DEVI NR. ChemInform Abstract: Expedient Approach to (2R,3S)-3-Azido-1,2-epoxy-4-phenylbutane: A Key Intermediate for HIV Protease Inhibitors. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199435128 |
0.293 |
|
| 2010 |
GURJAR MK, MAINKAR AS, SYAMALA M. ChemInform Abstract: Synthesis of C- α-D-Glucosyl-α-amino Acids. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199411254 |
0.4 |
|
| 2010 |
RAO AVR, GURJAR MK, NALLAGANCHU BR, BHANDARI A. ChemInform Abstract: Studies on Cyclodepsipeptides. Part 2. The Total Synthesis of Jaspamide and Geodiamolide-D. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199405253 |
0.405 |
|
| 2010 |
RAO AVR, GURJAR MK, NALLAGANCHU BR, BHANDARI A. ChemInform Abstract: Studies on Cyclodepsipeptides. Part 1. A Stereoselective Synthesis of C12 Polyketide Unit (C1-C8) Present in Jaspamide and Geodiamolide A-F. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199405045 |
0.32 |
|
| 2010 |
GURJAR MK, DEVI TR, REDDY KLN, SHARMA PA, DHAR TGM. ChemInform Abstract: Aureolic Acid Antibiotics: Synthesis of the Cyclohexenone Segment from D-Glucose. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199402284 |
0.361 |
|
| 2010 |
RAO AVR, REDDY KA, SRINIVAS NR, GURJAR MK, PADMAJA N, RAMAKUMAR S, VISWAMITRA MA, SWAPNA GVT, JAGANNADH B, KUNWAR AC. ChemInform Abstract: Chiral Polyhydroxylated Tetrahydrothiophene Derivatives: Novel Synthesis and Structural Elucidation by X-Ray Crystallography, NMR Spectroscopy and Molecular Mechanics Calculations. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199340182 |
0.318 |
|
| 2010 |
GURJAR MK, LALITHA SVS, SHARMA PA, RAO AVR. ChemInform Abstract: First Chemical Synthesis of Deuterated 3′-Azido-3′-deoxythymidine (AZT) . Cheminform. 24: no-no. DOI: 10.1002/CHIN.199317253 |
0.42 |
|
| 2010 |
GURJAR MK, SAHA UK. ChemInform Abstract: Synthesis of the Glycopeptide - O-(3,4-Di-O-methyl-2-O-(3,4-di-O- methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl)-L- alanilol: An Unusual Part Structure in the Glycopeptidolipid of Mycobacterium fortuitum. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199236257 |
0.324 |
|
| 2010 |
GURJAR MK, JOSHI SV, SASTRY BS, RAO AVR. ChemInform Abstract: A New Route to (.+-.)-Metoprolol (I). Cheminform. 22: no-no. DOI: 10.1002/CHIN.199130136 |
0.3 |
|
| 2010 |
RAO AV, GURJAR MK, BOSE DS, DEVI RR. ChemInform Abstract: A Simple Route to (2R,3R,5E)-2-Hydroxy-3-methyl-5-heptenal: A Key Intermediate for MeBmt. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199125116 |
0.31 |
|
| 2010 |
RAO AVR, GURJAR MK, SHARMA PA, KAIWAR V. ChemInform Abstract: Enantioselective Reductions of Ketones with Oxazaborolidines Derived from (R)- and (S)-α,α-Diphenyl-2-piperidinemethanol. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199110090 |
0.355 |
|
| 2010 |
RAO AVR, GURJAR MK, JOSHI SV. ChemInform Abstract: Sharpless Asymmetric Dihydroxylation of Aryloxy Allyl Ethers: A Simple Route to Chiral β-Blockers. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199108077 |
0.382 |
|
| 2010 |
GURJAR MK, REDDY AS. ChemInform Abstract: Stereoselective Synthesis of (9S,12R,13S)-Trihydroxyoctadeca-(10E,15Z)- dienoic Acid (I). Cheminform. 22: no-no. DOI: 10.1002/CHIN.199101348 |
0.389 |
|
| 2009 |
Mohapatra DK, Maity PK, Ghorpade RV, Gurjar MK. Syntheis of new chiral 5,6,7,8-tetrahydrotetrazolo[1,5-a]pyrazines from α-amino acid derivatives following "click" chemistry Heterocycles. 77: 865-872. DOI: 10.3987/COM-08-S(F)121 |
0.373 |
|
| 2009 |
Patil PS, Mahajan US, Sonawane SP, Gurjar MK. Short and Efficient Process for the Synthesis of trans-4-Aminocyclohexanecarboxylic Acid Derivatives Organic Process Research & Development. 13: 1141-1144. DOI: 10.1021/Op900195W |
0.488 |
|
| 2009 |
Chavan AB, Maikap GC, Gurjar MK. An efficient process of racemization of 3-(Carbamoylmethyl)-5- methylhexanoic acid: A pregabalin intermediate Organic Process Research and Development. 13: 812-814. DOI: 10.1021/Op900064X |
0.451 |
|
| 2009 |
Salunke GB, Shivakumar I, Gurjar MK. Total synthesis of verbalactone: an efficient, carbohydrate-based approach Tetrahedron Letters. 50: 2048-2049. DOI: 10.1016/J.Tetlet.2009.02.062 |
0.536 |
|
| 2009 |
Mohapatra DK, Chatterjee B, Gurjar MK. Highly stereoselective approach toward the synthesis of the macrolactone core of amphidinolide W Tetrahedron Letters. 50: 755-758. DOI: 10.1016/J.TETLET.2008.11.088 |
0.407 |
|
| 2009 |
Gurjar MK, Raghupathi N, Chorghade MS. ChemInform Abstract: A Short Total Synthesis of (+)-Cryptocarya Diacetate. Cheminform. 40. DOI: 10.1002/chin.200927196 |
0.441 |
|
| 2009 |
Gurjar MK, Reddy CN, Kalkote UR, Chorghade MS. ChemInform Abstract: Studies Toward the Total Synthesis of Carba Analogue of Motif C of M. TB Cell Wall AG Complex. Cheminform. 40. DOI: 10.1002/CHIN.200927183 |
0.312 |
|
| 2009 |
Mohapatra DK, Maity PK, Ghorpade RV, Gurjar MK. ChemInform Abstract: Synthesis of New Chiral 5,6,7,8-Tetrahydrotetrazolo[1,5-a]pyrazines from α-Amino Acid Derivatives Following “Click” Chemistry. Cheminform. 40. DOI: 10.1002/chin.200927160 |
0.436 |
|
| 2009 |
Mohapatra DK, Chatterjee B, Gurjar MK. ChemInform Abstract: Highly Stereoselective Approach Toward the Synthesis of the Macrolactone Core of Amphidinolide W. Cheminform. 40. DOI: 10.1002/chin.200919197 |
0.423 |
|
| 2009 |
Mohapatra DK, Bhattasali D, Gurjar MK, Khan MI, Shashidhara KS. ChemInform Abstract: First Asymmetric Total Synthesis of Penarolide Sulfate A1. Cheminform. 40. DOI: 10.1002/CHIN.200917173 |
0.342 |
|
| 2009 |
Chorghade MS, Mohapatra DK, Sahoo G, Gurjar MK, Mandlecha MV, Bhoite N, Moghe S, Raines RT. ChemInform Abstract: Practical Synthesis of 4-Fluoroprolines. Cheminform. 40. DOI: 10.1002/chin.200904183 |
0.558 |
|
| 2008 |
Chorghade MS, Mohapatra DK, Sahoo G, Gurjar MK, Mandlecha MV, Bhoite N, Moghe S, Raines RT. Practical syntheses of 4-fluoroprolines. Journal of Fluorine Chemistry. 129: 781-784. PMID 19727323 DOI: 10.1016/J.Jfluchem.2008.06.024 |
0.708 |
|
| 2008 |
Ramana CV, Khaladkar TP, Chatterjee S, Gurjar MK. Total synthesis and determination of relative and absolute configuration of multiplolide A. Journal of Organic Chemistry. 73: 3817-3822. PMID 18410146 DOI: 10.1021/Jo7027568 |
0.43 |
|
| 2008 |
Mohapatra DK, Rahaman H, Pal R, Gurjar MK. Total Synthesis of (S)-(-)-Curvularin: A Ring-Closing-Metathesis-Based Constructionof the Macrocyclic Framework Synlett. 2008: 1801-1804. DOI: 10.1055/S-2008-1078504 |
0.704 |
|
| 2008 |
Mohapatra DK, Sahoo G, Sankar K, Gurjar MK. Carbohydrate templates for the synthesis of prototype renin inhibitors Tetrahedron-Asymmetry. 19: 2123-2129. DOI: 10.1016/J.Tetasy.2008.08.007 |
0.684 |
|
| 2008 |
Mohapatra DK, Chatterjee B, Gurjar MK. Highly selective approach for the total synthesis of (+)-heliconol A Tetrahedron-Asymmetry. 19: 1568-1571. DOI: 10.1016/J.Tetasy.2008.05.031 |
0.688 |
|
| 2008 |
Mohapatra DK, Bhattasali D, Gurjar MK, Khan MI, Shashidhara KS. First Asymmetric Total Synthesis of Penarolide Sulfate A1 European Journal of Organic Chemistry. 2008: 6213-6224. DOI: 10.1002/EJOC.200800680 |
0.323 |
|
| 2008 |
Mohapatra DK, Rahaman H, Pal R, Gurjar MK. ChemInform Abstract: Total Synthesis of (S)-(-)-Curvularin (III): A Ring Closing Metathesis Based Construction of the Macrocyclic Framework. Cheminform. 39. DOI: 10.1002/CHIN.200848202 |
0.416 |
|
| 2008 |
Mohapatra DK, Maity PK, Chorghade MS, Gurjar MK. ChemInform Abstract: Synthesis of Unusual Tricyclic Ring Systems of Biological Interest. Cheminform. 39. DOI: 10.1002/CHIN.200819167 |
0.386 |
|
| 2008 |
Mohapatra DK, Pramanik C, Chorghade MS, Gurjar MK. ChemInform Abstract: A Short and Efficient Synthetic Strategy for the Total Syntheses of (S)-(+)- and (R)-(-)-Plakolide A. Cheminform. 39. DOI: 10.1002/CHIN.200807191 |
0.347 |
|
| 2007 |
Gurjar MK. The future lies in chiral purity: a perspective. Journal of the Indian Medical Association. 105: 177-8. PMID 17822185 |
0.282 |
|
| 2007 |
Gurjar MK, Pramanik C, Bhattasali D, Ramana CV, Mohapatra DK. Total syntheses of schulzeines B and C. The Journal of Organic Chemistry. 72: 6591-4. PMID 17630798 DOI: 10.1021/Jo070560H |
0.638 |
|
| 2007 |
Gurjar MK, Wakharkar RD, Singh AT, Jaggi M, Borate HB, Shinde PD, Verma R, Rajendran P, Dutt S, Singh G, Sanna VK, Singh MK, Srivastava SK, Mahajan VA, Jadhav VH, et al. Synthesis and evaluation of 4/5-hydroxy-2,3-diaryl(substituted)-cyclopent-2-en-1-ones as cis-restricted analogues of combretastatin A-4 as novel anticancer agents. Journal of Medicinal Chemistry. 50: 1744-53. PMID 17373779 DOI: 10.1021/Jm060938O |
0.273 |
|
| 2007 |
Mohapatra DK, Maity PK, Chorghade MS, Gurjar MK. Syntheis of unusual tricyclic ring systems of biological interest Heterocycles. 73: 269-274. DOI: 10.3987/COM-07-S(U)64 |
0.27 |
|
| 2007 |
Mohapatra DK, Maity PK, Gonnade RG, Chorghade MS, Gurjar MK. Synthesis of new chiral 4,5,6,7-tetrahydro[1,2,3]triazolo[1,5-a]pyrazines from α-amino acid derivatives under mild conditions Synlett. 1893-1896. DOI: 10.1055/s-2007-984537 |
0.422 |
|
| 2007 |
Mohapatra DK, Rahaman H, Chorghade MS, Gurjar MK. Synthesis of the C19-C34 segment of amphidinolide C Synlett. 2007: 567-570. DOI: 10.1055/S-2007-967968 |
0.675 |
|
| 2007 |
Ramana CV, Chaudhuri SR, Gurjar MK. Synthesis of L-ido-configured six-and seven-membered carba-sugars Synthesis. 2007: 523-528. DOI: 10.1055/S-2007-965899 |
0.351 |
|
| 2007 |
Ramana CV, Reddy BKK, Reddy CN, Gonnade RG, Gurjar MK. A Double Suzuki Approach for Synthesis of Substituted Diarylmethylidenefluorenes Synlett. 2007: 127-128. DOI: 10.1055/S-2006-958407 |
0.466 |
|
| 2007 |
Ramana CV, Mondal MA, Puranik VG, Gurjar MK. A carbohydrate based approach towards the synthesis of aspercyclide C Tetrahedron Letters. 48: 7524-7527. DOI: 10.1016/J.Tetlet.2007.08.050 |
0.548 |
|
| 2007 |
Mohapatra DK, Nayak S, Mohapatra S, Chorghade MS, Gurjar MK. Double intramolecular oxymercuration : the first stereoselective synthesis of the C10-C34 fragment of asimitrin Tetrahedron Letters. 48: 5197-5200. DOI: 10.1016/J.Tetlet.2007.05.147 |
0.715 |
|
| 2007 |
Mohapatra DK, Ramesh DK, Giardello MA, Chorghade MS, Gurjar MK, Grubbs RH. Protecting group directed ring-closing metathesis (RCM): the first total synthesis of an anti-malarial nonenolide Tetrahedron Letters. 48: 2621-2625. DOI: 10.1016/J.Tetlet.2007.02.040 |
0.729 |
|
| 2007 |
Ramana CV, Salian SR, Gurjar MK. Central core of uprolides D and E: a survey of some ring closing metathesis approaches Tetrahedron Letters. 48: 1013-1016. DOI: 10.1016/J.Tetlet.2006.11.176 |
0.42 |
|
| 2007 |
Mohapatra DK, Mondal D, Gurjar MK. Towards the Enantioselective Synthesis of anti-HIV Agents Litseaverticillols C and K from D-Glucose. Cheminform. 38. DOI: 10.1016/J.Tet.2007.01.037 |
0.697 |
|
| 2007 |
Mohapatra DK, Mondal D, Gurjar MK. Towards the enantioselective synthesis of anti-HIV agents litseaverticillols C and K from d-glucose Tetrahedron. 63: 2613-2621. DOI: 10.1016/J.TET.2007.01.037 |
0.664 |
|
| 2007 |
Mohapatra DK, Pramanik C, Chorghade MS, Gurjar MK. A Short and Efficient Synthetic Strategy for the Total Syntheses of (S)-(+)- and (R)-(–)-Plakolide A European Journal of Organic Chemistry. 2007: 5059-5063. DOI: 10.1002/EJOC.200700401 |
0.337 |
|
| 2007 |
Mohapatra DK, Maity PK, Gonnade RG, Chorghade MS, Gurjar MK. Synthesis of New Chiral 4,5,6,7-Tetrahydro[1,2,3]triazolo[1,5-a]pyrazines from α-Amino Acid Derivatives under Mild Conditions. Cheminform. 38. DOI: 10.1002/CHIN.200748151 |
0.422 |
|
| 2007 |
Ramana CV, Chaudhuri SR, Gurjar MK. Synthesis of L-ido-Configured Six- and Seven-Membered Carba-Sugars. Cheminform. 38. DOI: 10.1002/CHIN.200725190 |
0.363 |
|
| 2007 |
Ramana CV, Reddy BKK, Reddy CN, Gonnade RG, Gurjar MK. A Double Suzuki Approach for Synthesis of Substituted Diarylmethylidenefluorenes. Cheminform. 38. DOI: 10.1002/CHIN.200719106 |
0.432 |
|
| 2007 |
Gurjar MK, Mondal D, Ravindranadh SV, Chorghade MS. Clay-Mediated Selective Hydrolysis of 5′-O-Acetyl-2′,3′-isopropylidene/Cyclohexylidene Nucleosides. Cheminform. 38. DOI: 10.1002/CHIN.200707184 |
0.664 |
|
| 2007 |
Gurjar MK, Borhade RG, Puranik VG, Ramana CV. Total Synthesis of (-)-Radicamine B. Cheminform. 38. DOI: 10.1002/CHIN.200703180 |
0.343 |
|
| 2006 |
Gurjar MK, Mondal D, Ravindranadh SV, Chorghade MS. Clay‐Mediated Selective Hydrolysis of 5′‐O‐Acetyl‐2′,3′‐isopropylidene/Cyclohexylidene Nucleosides Synthetic Communications. 36: 2321-2327. DOI: 10.1080/00397910600639968 |
0.656 |
|
| 2006 |
Mohapatra DK, Mondal D, Chorghade MS, Gurjar MK. General strategy for a short and efficient synthesis of 3-hydroxy-4-methylprolines (HMP) Tetrahedron Letters. 47: 9215-9219. DOI: 10.1016/J.Tetlet.2006.10.137 |
0.8 |
|
| 2006 |
Gurjar MK, Borhade RG, Puranik VG, Ramana CV. Total synthesis of (−)-radicamine B Tetrahedron Letters. 47: 6979-6981. DOI: 10.1016/J.Tetlet.2006.07.120 |
0.355 |
|
| 2006 |
Mohapatra DK, Mondal D, Gonnade RG, Chorghade MS, Gurjar MK. Synthesis of the spiro fused β-lactone-γ-lactam segment of oxazolomycin Tetrahedron Letters. 47: 6031-6035. DOI: 10.1016/J.Tetlet.2006.06.117 |
0.782 |
|
| 2006 |
Mohapatra DK, Mohapatra S, Gurjar MK. Double intramolecular oxymercuration: stereoselective synthesis of highly substituted bis-tetrahydrofuran Tetrahedron Letters. 47: 5943-5947. DOI: 10.1016/J.Tetlet.2006.06.049 |
0.714 |
|
| 2006 |
Ramana CV, Mondal MA, Puranik VG, Gurjar MK. Synthetic studies toward macrocidins: an RCM approach for the construction of the central cyclic core Tetrahedron Letters. 47: 4061-4064. DOI: 10.1016/J.Tetlet.2006.03.192 |
0.451 |
|
| 2006 |
Ramana CV, Mallik R, Gonnade RG, Gurjar MK. Palladium mediated cycloisomerization of sugar alkynols: synthesis of cyclic enol-ethers and spiroketals Tetrahedron Letters. 47: 3649-3652. DOI: 10.1016/J.Tetlet.2006.03.143 |
0.48 |
|
| 2006 |
Yakambram P, Puranik VG, Gurjar MK. Towards the total synthesis of clavosolide A Tetrahedron Letters. 47: 3781-3783. DOI: 10.1016/J.Tetlet.2006.03.107 |
0.508 |
|
| 2006 |
Mohapatra DK, Chaudhuri SR, Sahoo G, Gurjar MK. Stereoselective synthesis of the polyketide chain of nagahamide A Tetrahedron-Asymmetry. 17: 2609-2616. DOI: 10.1016/J.Tetasy.2006.09.025 |
0.715 |
|
| 2006 |
Kalkote UR, Purude AN, Puranik VG, Gurjar MK. A convenient chemoenzymatic synthesis of (1S,7aS)-1-hydroxy-5-oxo-4-(2′-carboxyethyl)-7a-methyltetrahydro-indane—a key intermediate of steroids Journal of Molecular Catalysis B-Enzymatic. 40: 38-43. DOI: 10.1016/J.Molcatb.2006.01.037 |
0.381 |
|
| 2006 |
Kar P, Nagaiah K, Gurjar MK. Radical Opening Reaction of Glucosyl 1,2-Cyclopropane Derivatives: Synthesis of α and β C-Glycosides and Oxepane Derivatives. Cheminform. 37. DOI: 10.1002/CHIN.200611209 |
0.411 |
|
| 2005 |
Ramana CV, Srinivas B, Puranik VG, Gurjar MK. A carbohydrate-based approach for the total synthesis of 1,3-polyol/α-pyrone antifungal natural products Journal of Organic Chemistry. 70: 8216-8219. PMID 16277353 DOI: 10.1021/Jo050972V |
0.469 |
|
| 2005 |
Gurjar MK, Karumudi B, Ramana CV. Synthesis of eupomatilone-6 and assignment of its absolute configuration Journal of Organic Chemistry. 70: 9658-9661. PMID 16268656 DOI: 10.1021/Jo0516234 |
0.497 |
|
| 2005 |
Gurjar MK, Nagaprasad R, Ramana CV, Karmakar S, Mohapatra DK. Ring-closing metathesis mediated total synthesis of microcarpalide and herbarumin III Arkivoc. 2005. DOI: 10.3998/Ark.5550190.0006.326 |
0.682 |
|
| 2005 |
Murugan A, Yadav AK, Gurjar MK. Stereoselective syntheses of (+)-proto, (-)-gala quercitols and carba-l-rhamnose from d-(-)-quinic acid Tetrahedron Letters. 46: 6235-6238. DOI: 10.1016/J.Tetlet.2005.07.052 |
0.435 |
|
| 2005 |
Hotha S, Maurya SK, Gurjar MK. Stereoselective synthesis of spiroannulated cyclopentenones by the Pauson-Khand reaction on carbohydrate derived enynes Tetrahedron Letters. 46: 5329-5332. DOI: 10.1016/j.tetlet.2005.06.013 |
0.675 |
|
| 2005 |
Ramana CV, Raghupathi N, Gurjar MK, Chorghade MS. A carbohydrate-based approach for the total synthesis of strictifolione Tetrahedron Letters. 46: 4073-4075. DOI: 10.1016/J.Tetlet.2005.04.031 |
0.44 |
|
| 2005 |
Gurjar MK, Nayak S, Ramana CV. Synthetic studies toward tricyclic cembranoids: A modular approach for the construction of the tricyclic framework of eunicin Tetrahedron Letters. 46: 1881-1884. DOI: 10.1016/J.Tetlet.2005.01.094 |
0.47 |
|
| 2005 |
Joshi RA, Garud DR, Muthukrishnan M, Joshi RR, Gurjar MK. A convenient synthesis of the enantiomerically pure β-blocker (S)-betaxolol using hydrolytic kinetic resolution Tetrahedron-Asymmetry. 16: 3802-3806. DOI: 10.1016/J.Tetasy.2005.10.028 |
0.46 |
|
| 2005 |
Kumar P, Deshmukh AN, Upadhyay RK, Gurjar MK. A simple and practical approach to enantiomerically pure (S)-3-hydroxy-γ-butyrolactone: synthesis of (R)-4-cyano-3-hydroxybutyric acid ethyl ester Tetrahedron-Asymmetry. 16: 2717-2721. DOI: 10.1016/J.Tetasy.2005.07.012 |
0.488 |
|
| 2005 |
Gurjar MK, Rao BV, Krishna LM, Chorghade MS, Ley SV. Stereoselective synthesis of (2S,7S)-7-(4-phenoxymethyl)-2-(1-N-hydroxyureidyl-3-butyn-4-yl)oxepane: a potential anti-asthmatic drug candidate Tetrahedron: Asymmetry. 16: 935-939. DOI: 10.1016/J.Tetasy.2005.01.024 |
0.494 |
|
| 2005 |
Maurya SK, Patil P, Umbarkar SB, Gurjar MK, Dongare M, Rudiger S, Kemnitz E. Vapor phase oxidation of 4-fluorotoluene over vanadia-titania catalyst Journal of Molecular Catalysis a-Chemical. 234: 51-57. DOI: 10.1016/J.Molcata.2005.02.020 |
0.366 |
|
| 2005 |
Hotha S, Maurya SK, Gurjar MK. Stereoselective Synthesis of Spiroannulated Cyclopentenones by the Pauson—Khand Reaction on Carbohydrate-Derived Enynes. Cheminform. 36. DOI: 10.1002/CHIN.200546185 |
0.694 |
|
| 2005 |
Ramana CV, Raghupathi N, Gurjar MK, Chorghade MS. A Carbohydrate-Based Approach for the Total Synthesis of Strictifolione. Cheminform. 36. DOI: 10.1002/CHIN.200540198 |
0.382 |
|
| 2005 |
Gurjar MK, Rao BV, Krishna LM, Chorghade MS, Ley SV. Stereoselective Synthesis of (2S,7S)-7-(4-Phenoxymethyl)-2-(1-N-hydroxyureidyl-3-butyn-4-yl)oxepane: A Potential Antiasthmatic Drug Candidate. Cheminform. 36. DOI: 10.1002/chin.200530155 |
0.316 |
|
| 2005 |
Gurjar MK, Mohapatra S, Phalgune UD, Puranik VG, Mohapatra DK. Towards the Total Synthesis of Amphidinolide E (I): An Enantioselective Synthesis of C12?C29 Fragment (II). Cheminform. 36. DOI: 10.1002/CHIN.200504212 |
0.389 |
|
| 2005 |
Wakharkar RD, Sahasrabuddhe MB, Borate HB, Gurjar MK. Selective Cleavage of 2,3-O-Isopropylidene Group: A Case of Anchimeric Assistance from O-Glycoside. Cheminform. 36. DOI: 10.1002/chin.200501175 |
0.245 |
|
| 2005 |
Kar P, Rao BV, Sarma JARP, Chowdhury B, Nagaiah K, Gurjar MK. A review of synthetic and molecular model study towards fixing up bio-active chiral centre at C28 of Lasonolide-A, an anticancer macrolide: A new chiral pool approach Journal of the Indian Chemical Society. 82: 534-537. |
0.352 |
|
| 2004 |
Gurjar MK, Cherian J, Ramana CV. Synthesis of the putative structure of eupomatilone-6. Organic Letters. 6: 317-9. PMID 14748582 DOI: 10.1021/Ol035908J |
0.406 |
|
| 2004 |
Wakharkar RD, Sahasrabuddhe MB, Borate HB, Gurjar MK. Selective Cleavage of 2,3-O-Isopropylidene Group: A Case of Anchimeric Assistance from O-Glycoside Synthesis. 2004: 1830-1834. DOI: 10.1055/S-2004-829128 |
0.264 |
|
| 2004 |
Gurjar MK, Mohapatra S, Phalgune UD, Puranik VG, Mohapatra DK. Towards the total synthesis of amphidinolide E: an enantioselective synthesis of C12-C29 fragment Tetrahedron Letters. 45: 7899-7902. DOI: 10.1016/J.Tetlet.2004.08.143 |
0.702 |
|
| 2004 |
Dongare MK, Bhagwat VV, Ramana CV, Gurjar MK. Silica supported MoO3: A mild heterogeneous catalyst for the Beckmann rearrangement and its application to some sugar derived ketoximes Tetrahedron Letters. 45: 4759-4762. DOI: 10.1016/J.Tetlet.2004.04.068 |
0.282 |
|
| 2004 |
Gurjar MK, Karmakar S, Mohapatra DK. First total synthesis of herbarumin III Tetrahedron Letters. 45: 4525-4526. DOI: 10.1016/J.TETLET.2004.04.040 |
0.402 |
|
| 2004 |
Ramana CV, Reddy BS, Gurjar MK. Synthesis of differentially protected cyclopentitol: Its application towards the stereoselective synthesis of 5-epi-calditol Tetrahedron Letters. 45: 2817-2819. DOI: 10.1016/J.Tetlet.2004.02.020 |
0.539 |
|
| 2004 |
Gurjar MK, Pedduri Y, Ramana CV, Puranik VG, Gonnade RG. Toward a synthesis of the antitumor macrolide peloruside A: a chiral pool approach for the C(1)-C(11) segment Tetrahedron Letters. 45: 387-390. DOI: 10.1016/J.Tetlet.2003.10.153 |
0.508 |
|
| 2004 |
Joshi RA, Patil PS, Muthukrishnan M, Ramana CV, Gurjar MK. Copper-mediated coupling of aminopurines and aminopyrimidines with arylboronic acids Tetrahedron Letters. 45: 195-197. DOI: 10.1016/J.Tetlet.2003.10.088 |
0.331 |
|
| 2004 |
Gurjar MK, Reddy DS, Bhadbhade MM, Gonnade RG. Diastereoselective Reformatsky reaction of methyl 4-bromocrotonate with 1,2:5,6-di-O-isopropylidene-α-d-ribo-hexofuranos-3-ulose: application to novel bicyclic nucleosides Tetrahedron. 60: 10269-10275. DOI: 10.1016/J.Tet.2004.08.092 |
0.518 |
|
| 2004 |
Gurjar MK, Talukdar A. Synthesis of terminal disaccharide unit of Klebsiella pneumoniae ssp. R20 Tetrahedron. 60: 3267-3271. DOI: 10.1016/J.Tet.2004.02.017 |
0.517 |
|
| 2004 |
Dongare MK, Bhagwat VV, Ramana CV, Gurjar MK. Silica-Supported MoO3: A Mild Heterogeneous Catalyst for the Beckmann Rearrangement and Its Application to Some Sugar-Derived Ketoximes. Cheminform. 35. DOI: 10.1002/CHIN.200438046 |
0.268 |
|
| 2004 |
Gurjar MK, Karmakar S, Mohapatra DK. First Total Synthesis of Herbarumin III. Cheminform. 35. DOI: 10.1002/CHIN.200437216 |
0.402 |
|
| 2004 |
Joshi RA, Patil PS, Muthukrishnan M, Ramana CV, Gurjar MK. Copper-Mediated Coupling of Aminopurines and Aminopyrimidines with Arylboronic Acids. Cheminform. 35. DOI: 10.1002/CHIN.200414060 |
0.273 |
|
| 2003 |
Gurjar MK, Ravindranadh SV, Sankar K, Karmakar S, Cherian J, Chorghade MS. Synthesis of spirocycles via ring closing metathesis of heterocycles carrying gem-diallyl substituents obtained via ring opening of (halomethyl)cyclopropanes with allyltributyltin. Organic & Biomolecular Chemistry. 1: 1366-73. PMID 12929667 |
0.437 |
|
| 2003 |
Gurjar MK, Bera S, Joshi RR, Joshi RA. Synthesis of rigid bicycloheterocyclic scaffolds from Vince's lactam (enzymatic resolution of Vince's lactam) Heterocycles. 60: 2293-2303. DOI: 10.3987/Com-03-9841 |
0.468 |
|
| 2003 |
Maurya SK, Gurjar MK, Malshe KM, Patil PT, Dongare MK, Kemnitz E. Solid acid catalysts for fluorotoluene nitration using nitric acid Green Chemistry. 5: 720-723. DOI: 10.1039/B307146D |
0.402 |
|
| 2003 |
Gurjar MK, Ravindranadh SV, Sankar K, Karmakar S, Cherian J, Chorghade MS. Synthesis of spirocycles via ring closing metathesis of heterocycles carrying gem-diallyl substituents obtained via ring opening of (halomethyl)cyclopropanes with allyltributyltin Organic and Biomolecular Chemistry. 1: 1366-1373. DOI: 10.1039/b300314k |
0.437 |
|
| 2003 |
Gurjar MK, Murugaiah AMS, Reddy DS, Chorghade MS. A new route to prepare 6-chloro-5-(2-chloroethyl)oxindole Organic Process Research and Development. 7: 309-312. DOI: 10.1021/Op020095K |
0.502 |
|
| 2003 |
Gurjar MK, Murugaiah AMS, Radhakrishna P, Ramana CV, Chorghade MS. A novel and simple asymmetric synthesis of CMI-977 (LDP-977): A potent anti-asthmatic drug lead Tetrahedron Asymmetry. 14: 1363-1370. DOI: 10.1016/S0957-4166(03)00157-5 |
0.455 |
|
| 2003 |
Gurjar MK, Khaladkar TP, Borhade RG, Murugan A. Carbohydrate-based synthesis of crocacin: Stereoselective Heck reaction of carbohydrate 5,6-ene- and 5,6-yne-derivatives with aromatic halides Tetrahedron Letters. 44: 5183-5187. DOI: 10.1016/S0040-4039(03)01256-5 |
0.494 |
|
| 2003 |
Gurjar MK, Joshi RA, Chaudhuri SR, Joshi SV, Barde AR, Gediya LK, Ranade PV, Kadam SM, Naik SJ. Total synthesis of cis and trans-hydroxyglimepiride: active metabolite of glimepiride Tetrahedron Letters. 44: 4853-4855. DOI: 10.1016/S0040-4039(03)01145-6 |
0.321 |
|
| 2003 |
Gurjar MK, Nagaprasad R, Ramana CV. Total synthesis of microcarpalide Tetrahedron Letters. 44: 2873-2875. DOI: 10.1016/S0040-4039(03)00441-6 |
0.537 |
|
| 2003 |
Sharma GVM, Ilangovan A, Narayanan VL, Gurjar MK. First synthesis of aza-calanolides-a new class of anti-HIV active compounds Tetrahedron. 59: 95-99. DOI: 10.1016/S0040-4020(02)01456-4 |
0.405 |
|
| 2003 |
Gurjar MK, Joshi RA, Chaudhuri SR, Joshi SV, Barde AR, Gediya LK, Ranade PV, Kadam SM, Naik SJ. Total Synthesis of cis and trans-Hydroxyglimepiride: Active Metabolite of Glimepiride. Cheminform. 34. DOI: 10.1002/CHIN.200339078 |
0.321 |
|
| 2003 |
Gurjar MK, Murugaiah AMS, Radhakrishna P, Ramana CV, Chorghade MS. A Novel and Simple Asymmetric Synthesis of CMI-977 (LDP-977): A Potent anti-Asthmatic Drug Lead. Cheminform. 34. DOI: 10.1002/CHIN.200337093 |
0.344 |
|
| 2003 |
Chorghade MS, Gurjar MK, Talukdar A. Fascinating Excursions into Chiral Chemistry: An Insider′s Perspective Cheminform. 34. DOI: 10.1002/CHIN.200336253 |
0.331 |
|
| 2003 |
Sharma GVM, Ilangovan A, Narayanan VL, Gurjar MK. First Synthesis of Aza-Calanolides — A New Class anti-HIV Active Compounds. Cheminform. 34. DOI: 10.1002/CHIN.200320238 |
0.296 |
|
| 2002 |
Gurjar MK, Bera S. Carbohydrate-based synthesis of naturally occurring marine metabolites slagenins B and C. Organic Letters. 4: 3569-70. PMID 12375889 |
0.385 |
|
| 2002 |
Grilli S, Lunazzi L, Mazzanti A, Pinamonti M, Anderson JE, Ramana CV, Koranne PS, Gurjar MK. Conformational studies by dynamic NMR. 91. Conformational stereodynamics of tetraethylmethane and analogous C(CH2X)4 compounds. The Journal of Organic Chemistry. 67: 6387-94. PMID 12201759 DOI: 10.1021/Jo025984K |
0.28 |
|
| 2002 |
Ramana CV, Baquer SM, Gonnade RG, Gurjar MK. An expedient synthesis of tetrakis(cyclopropylmethyl)methane. Chemical Communications. 614-5. PMID 12120149 DOI: 10.1039/B110246J |
0.369 |
|
| 2002 |
Gurjar MK, Maheshwar K. Stereoselective synthesis of a novel carbocyclic nucleoside. The Journal of Organic Chemistry. 66: 7552-4. PMID 11681980 DOI: 10.1021/JO010718C |
0.486 |
|
| 2002 |
Gurjar MK, Talukdar A. Heck reaction of (S)-N-Cbz-allyl glycine t-butyl ester with aromatic halides Synthesis. 2002: 315-316. DOI: 10.1055/S-2002-20046 |
0.411 |
|
| 2002 |
Gurjar MK, Nagaprasad R, Ramana CV. First synthesis of methyl α-C-D-arabinofuranosyl-(1→5)-α-D-arabinofuranoside: The C-disaccharide segment of motif C of Mycobacterium tuberculosis Tetrahedron Letters. 43: 7577-7579. DOI: 10.1016/S0040-4039(02)01760-4 |
0.47 |
|
| 2002 |
Gurjar MK, Chaudhuri SR. A stereoselective synthesis of the C13C19 fragment of sanglifehrin A Tetrahedron Letters. 43: 2435-2438. DOI: 10.1016/S0040-4039(02)00191-0 |
0.488 |
|
| 2002 |
Gurjar MK, Karmakar S, Mohapatra DK, Phalgune UD. A novel application of a [3+2] cycloaddition reaction for the synthesis of the piperazinone rings of pseudotheonamides A 1 and A 2 Tetrahedron Letters. 43: 1897-1900. DOI: 10.1016/S0040-4039(02)00133-8 |
0.427 |
|
| 2002 |
Gurjar MK, Reddy DS. Carbohydrate based formal synthesis of stemoamide using ring-closing metathesis Tetrahedron Letters. 43: 295-298. DOI: 10.1016/S0040-4039(01)02052-4 |
0.506 |
|
| 2001 |
Gurjar MK, Reddy LK, Hotha S. Synthesis of ethyl 5-O-(alpha-D-arabinofuranosyl)-6-O-(beta-D-galactofuranosyl)-beta-D- galactofuranoside present in motif E of the Mycobacterium tuberculosis cell wall. Organic Letters. 3: 321-3. PMID 11428004 DOI: 10.1021/OL0002976 |
0.623 |
|
| 2001 |
Gurjar MK, Reddy LK, Hotha S. Synthesis of oligosaccharides of motifs D and E of arabinogalactan present in Mycobacterium tuberculosis. The Journal of Organic Chemistry. 66: 4657-60. PMID 11421788 DOI: 10.1021/JO010180A |
0.631 |
|
| 2001 |
Gurjar MK, Cherian J. Studies toward Unique Mycolactone Macrolides from Mycobacterium ulcerans Heterocycles. 55: 1095-1103. DOI: 10.3987/Com-01-9199 |
0.321 |
|
| 2001 |
Gurjar Mk, Reddy R. UNUSUAL FORMATION OF 2-BUTYL-5-ALKYLOXYMETHYLFURAN Synthetic Communications. 31: 3481-3484. DOI: 10.1081/SCC-100106208 |
0.254 |
|
| 2001 |
Gurjar MK, Ravindranadh SV, Kumar P. 5-Exo-dig, 5-exo-trig cascade radical cyclisation on sugar-furanose templates: entry to angularly fused oxa- and dioxa-triquinane skeletons Chemical Communications. 917-918. DOI: 10.1039/B101641P |
0.393 |
|
| 2001 |
Gurjar MK, Yakambram P. Temperature-dependent isomerisation versus net fragmentation of secondary allylic alcohols with Grubbs’ catalyst Tetrahedron Letters. 42: 3633-3636. DOI: 10.1016/S0040-4039(01)00449-X |
0.386 |
|
| 2001 |
Gurjar MK, Reddy LK, Hotha S. ChemInform Abstract: Synthesis of Ethyl 5-O-(α-D-Arabinofuranosyl)-6-O- (β-D-galactofuranosyl)-β-D-galactofuranoside Present in Motif E of the Mycobacterium tuberculosis Cell Wall. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200120176 |
0.647 |
|
| 2001 |
Gurjar MK, Ravindranadh SV, Karmakar S. ChemInform Abstract: Mild and Efficient Methodology for Installation of gem-Diallyl Functionality on Carbohydrate Synthons. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200120174 |
0.314 |
|
| 2001 |
Gurjar M, Reddy DS, Murugaiah A, Murugaiah S. ChemInform Abstract: Bis(dealkoxycarbonylation) of Nitroarylmalonates: A Facile Entry to Alkylated Nitroaromatics. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200108113 |
0.367 |
|
| 2001 |
Gurjar MK, Hotha S. ChemInform Abstract: Towards the Synthesis of Scyphostatin. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200106199 |
0.71 |
|
| 2000 |
Gurjar MK, Krishna LM, Reddy BS, Chorghade MS. A Versatile Approach to Anti-Asthmatic Compound CMI-977 and its Six-Membered Analogue Synthesis. 2000: 557-560. DOI: 10.1055/S-2000-6376 |
0.266 |
|
| 2000 |
Gurjar M, Reddy DS, Murugaiah A, Murugaiah S. Bis(dealkoxycarbonylation) of nitroarylmalonates: A facile entry to alkylated nitroaromatics Synthesis. 1659-1661. |
0.423 |
|
| 1999 |
Gurjar MK, Pal S, Mohapatra DK. A New Stereoselective Synthetic Strategy For Beta -Hydroxy-Alpha -Amino Acids Of Vancomycin Heterocycles. 50: 109-116. DOI: 10.3987/Com-98-8204 |
0.62 |
|
| 1999 |
Chorghade MS, Gurjar MK, Adhikari S, Sadalapure K, Lalitha SVS, Murugaiah AMS, Krishna PR. Synthesis of (2S, 5S)- trans-5-(4- fluorophenoxymethyl) -2-(1-N-hydroxy ureidyl-3-butyn-4-yl) -tetrahydrofuran– (CMI-977) Pure and Applied Chemistry. 71: 1071-1074. DOI: 10.1351/Pac199971061071 |
0.39 |
|
| 1999 |
Gurjar MK, Kumar VS, Rao BV. Synthesis of a new type of antitumour agent panaxytriol: Synthesis of its four diastereomers Tetrahedron. 55: 12563-12576. DOI: 10.1016/S0040-4020(99)00732-2 |
0.516 |
|
| 1998 |
Gurjar MK, Sadalapure K, Adhikari S, Sarma BVNBS, Talukdar A, Chorghade MS. Kinetic Resolution Of Aryl Glycidyl Ethers: A Practical Synthesis Of Optically Pure Beta -Blocker - S-Metoprolol Heterocycles. 48: 1471-1476. DOI: 10.3987/Com-98-8169 |
0.409 |
|
| 1998 |
Gurjar MK, Lalitha SVS. Studies directed toward anti-HIV compounds Pure and Applied Chemistry. 70: 303-306. DOI: 10.1351/pac199870020303 |
0.219 |
|
| 1998 |
Gurjar MK, Sharma BVNBS, Rao BV. Synthesis and Application of 3,3-Spirocyclopropane Derivatives Obtained from 1,2:5,6-Di-O-Isopropylidene-α-D-Glucofuranose Journal of Carbohydrate Chemistry. 17: 1107-1115. DOI: 10.1080/07328309808001887 |
0.536 |
|
| 1998 |
Gurjar MK, Sarma BVNBS, Sadalapure K, Adhikari S. A Practical Synthesis of (R)- and (S)-Benzylglycidols by Hydrolytic Kinetic Resolution Synthesis. 1998: 1424-1424. DOI: 10.1055/S-1998-2179 |
0.436 |
|
| 1998 |
Mereyala HB, Hotha S, Gurjar MK. Synthesis of pentaarabinofuranosyl structure motif A of Mycobacterium tuberculosis Chemical Communications. 685-686. DOI: 10.1039/A707796C |
0.657 |
|
| 1998 |
Gurjar MK, Krishna LM, Sarma aBVNBS, Chorghade MS. A Practical Synthesis of (R)-(−)-Phenylephrine Hydrochloride Organic Process Research & Development. 2: 422-424. DOI: 10.1021/Op970128+ |
0.431 |
|
| 1998 |
Gurjar MK, Rajendran V, Rao BV. Chiron approach towards a potent toxin fumonisin B1 backbone: Synthesis of its hexaacetate derivative Tetrahedron Letters. 39: 3803-3806. DOI: 10.1016/S0040-4039(98)00588-7 |
0.469 |
|
| 1997 |
Gurjar MK, Pal S, Rao AVR. Studies Directed toward the Synthesis of Martinellines : One Pot Synthesis of Pyrroloquinolone Ring System Heterocycles. 45: 231-234. DOI: 10.3987/Com-96-7638 |
0.537 |
|
| 1997 |
Gurjar MK, Chakrabarti A, Rao AVR. A Stereocontrolled Synthesis Of Pironetin Heterocycles. 45: 7-10. DOI: 10.3987/Com-96-7631 |
0.547 |
|
| 1997 |
Rao BV, Krishna UM, Gurjar MK. Stereoselective Synthesis of [2S,3R]-β-Hydroxy Ornithine Synthetic Communications. 27: 1335-1345. DOI: 10.1080/00397919708006062 |
0.467 |
|
| 1997 |
Rao AVR, Gurjar MK, Lakshmipathi P, Reddy MM, Nagarajan M, Pal S, Sarma BVNBS, Tripathy NK. SNAr Macrocyclisation : A New Approach Towards the Synthesis of D-O-E- Segment of Vancomycin Tetrahedron Letters. 38: 7433-7436. DOI: 10.1016/S0040-4039(97)01749-8 |
0.463 |
|
| 1997 |
Gurjar MK, Chakrabarti A, Rao BV, Kumar P. Preparation of 4,5-cyclopropylsugar derivatives : application to the stereocontrolled synthesis of bottom half (C7-C16) segment of lasonolide A Tetrahedron Letters. 38: 6885-6888. DOI: 10.1016/S0040-4039(97)01586-4 |
0.484 |
|
| 1997 |
Bose DS, Srinivas P, Gurjar MK. Stereospecific synthesis of a novel azetido[2,1-c][1,4]-benzodiazepine (ABD) ring system with DNA recognition potential Tetrahedron Letters. 38: 5839-5842. DOI: 10.1016/S0040-4039(97)01297-5 |
0.471 |
|
| 1997 |
Gurjar MK, Tripathy NK. Synthesis of CC biaryl segment of complestatin and chloropeptin: Approach to the right hand CEF-ring system of complestatin Tetrahedron Letters. 38: 2163-2166. DOI: 10.1016/S0040-4039(97)00272-4 |
0.416 |
|
| 1997 |
Gurjar MK, Adhikari S. Synthesis of the unique terminal branched tetrasaccharide of Mycobacterium gordonae strain 990 Tetrahedron. 53: 8629-8634. DOI: 10.1016/S0040-4020(97)00532-2 |
0.452 |
|
| 1997 |
Gurjar MK, Pal S, Rao AVR, Pariza RJ, Chorghade MS. Synthesis of novel C2-symmetric and pseudo C2-symmetric based diols, epoxides and dideoxy derivatives of HIV protease inhibitors Tetrahedron. 53: 4769-4778. DOI: 10.1016/S0040-4020(97)00160-9 |
0.491 |
|
| 1996 |
Rao AVR, Gurjar MK, Ramana DV, Chheda AK. Synthesis Of Optically Active O,O,O-Trimethylkorupen-Samines A And B Heterocycles. 43: 1-6. DOI: 10.3987/Com-95-7243 |
0.378 |
|
| 1996 |
Gurjar MK, Kumar P, Rao BV. Stereocontrolled synthesis of spirocyclopropane sugars and their application to asymmetric formation of tertiary chiral centres: A route to 2,2′-dialkylated pyranose subunit (C18C23) of lasonolide A Tetrahedron Letters. 37: 8617-8620. DOI: 10.1016/0040-4039(96)01991-0 |
0.532 |
|
| 1996 |
Gurjar MK, Henri JT, Bose DS, Rao AVR. Total synthesis of a potent immunosuppressant pironetin Tetrahedron Letters. 37: 6615-6618. DOI: 10.1016/0040-4039(96)01413-X |
0.526 |
|
| 1995 |
Swamy GYSK, Ravikumar K, Rama Rao AV, Gurjar MK, Ramadevi T. An Oxazolidinone Derivative of D-Furanose Acta Crystallographica Section C Crystal Structure Communications. 51: 426-428. DOI: 10.1107/S0108270194003732 |
0.29 |
|
| 1995 |
Rama Rao AV, Gurjar MK, Vasudevan J. An enantiospecific synthesis of the tricyclic guanidine segment of the anti-HIV marine alkaloid batzelladine A Journal of the Chemical Society - Series Chemical Communications. 1369-1370. DOI: 10.1039/C39950001369 |
0.424 |
|
| 1995 |
Rao AVR, Gurjar MK, Reddy KL, Rao AS. Studies directed toward the synthesis of vancomycin and related cyclic peptides Chemical Reviews. 95: 2135-2167. DOI: 10.1021/Cr00038A014 |
0.399 |
|
| 1995 |
Gurjar MK, Mainkar AS, Srinivas P. Stereoselective synthesis of C3C9 segment of soraphen A Tetrahedron Letters. 36: 5967-5968. DOI: 10.1016/0040-4039(95)01154-A |
0.465 |
|
| 1995 |
Rao AR, Gurjar MK, Pal S, Pariza RJ, Chorghade MS. Synthesis of a novel C2-symmetrical (2S,5S)-2,5-bis-[(1,1-dimethylethoxy)carbonylamino]-1,6-diphenylhex-3-ene: Applications in the synthesis of potential HIV protease inhibitors Tetrahedron Letters. 36: 2505-2508. DOI: 10.1016/0040-4039(95)00255-B |
0.467 |
|
| 1995 |
Gurjar MK, Das SK, Kunwar AC. Studies towards the synthesis of the highly oxygenated bicyclic core of zaragozic acid1: Incorporation of three quaternary chiral carbon centres☆ Tetrahedron Letters. 36: 1937-1940. DOI: 10.1016/0040-4039(95)00161-5 |
0.459 |
|
| 1995 |
Gurjar MK, Das SK, Sadalapure KS. Zaragozic acid: Unusual stereochemical dependence in anhydride formation of carbohydrate templates Tetrahedron Letters. 36: 1933-1936. DOI: 10.1016/0040-4039(95)00160-E |
0.467 |
|
| 1995 |
GURJAR MK, GHOSH L, SYAMALA M, JAYASREE V. ChemInform Abstract: Stereoselective Synthesis of (+)- and (-)-Lentiginosine. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199516306 |
0.486 |
|
| 1994 |
Gurjar MK, Das SK, Mainkar PS. Synthesis of Terminal Oligosaccharides from Type Specific Lipooligosaccharide of Mycobacterium Tuberculosis Journal of Carbohydrate Chemistry. 13: 899-907. DOI: 10.1080/07328309408011690 |
0.445 |
|
| 1994 |
Rao AVR, Gurjar MK, Lalitha SVS. Discovery of a novel route to β-thymidine: a precursor for anti-AIDS compounds Journal of the Chemical Society, Chemical Communications. 1255-1256. DOI: 10.1039/C39940001255 |
0.399 |
|
| 1994 |
Gurjar M, Ghosh L, Syamala M, Jayasree V. Stereoselective synthesis of (+)- and (-)-lentiginosine Tetrahedron Letters. 35: 8871-8872. DOI: 10.1016/S0040-4039(00)78520-0 |
0.341 |
|
| 1994 |
Gurjar MK, Das SK, Saha UK. Zaragozic acid A : interesting observations in anhydro-ring formation of densely functionalised carbohydrate templates Tetrahedron Letters. 35: 2241-2244. DOI: 10.1016/S0040-4039(00)76809-2 |
0.47 |
|
| 1994 |
Gurjar MK, Devi NR. An expedient approach to (2R,3S)-3-azido-1,2-epoxy-4-phenyl butane : a key intermediate for HIV protease inhibitors Tetrahedron-Asymmetry. 5: 755-758. DOI: 10.1016/0957-4166(94)80039-1 |
0.505 |
|
| 1993 |
Gurjar MK, Mainkar PS. Synthesis of methyl 3-O-(2-O-methyl-α-l-fucopyranosyl)-α-l-rhamnopyranoside, methyl 3-O-α-l-rhamnopyranosyl-α-d-glucopyranoside, and methyl 3-O-[3-O-(2-O-methyl-α-l-fucopyranosyl)-α-l-rhamnopyranosyl]-α-l-rhamnopyranoside: di- and tri-saccharide segments of a lipo-oligosaccharide (LOS-1) of Mycobacterium szulgai Carbohydrate Research. 239: 297-304. PMID 8457999 DOI: 10.1016/0008-6215(93)84227-W |
0.42 |
|
| 1993 |
Gurjar MK, Srinivas NR. Synthesis of the terminal trisaccharide unit of the lipo-oligosaccharide from Mycobacterium linda Carbohydrate Research. 247: 309-313. PMID 8221724 DOI: 10.1016/0008-6215(93)84264-7 |
0.478 |
|
| 1993 |
Gurjar MK, Reddy KR. Synthesis of the oligosaccharide segment of a novel phenolic glycolipid antigen from Mycobacterium haemophilum Journal of the Chemical Society-Perkin Transactions 1. 1269-1272. DOI: 10.1039/P19930001269 |
0.511 |
|
| 1993 |
Rao AVR, Reddy KA, Srinivas NR, Gurjar MK, Padmaja N, Ramakumar S, Viswamitra MA, Swapna GVT, Jagannadh B, Kunwar AC. Chiral polyhydroxylated tetrahydrothiophene derivatives: novel synthesis and structural elucidation by X-ray crystallography, NMR spectroscopy and molecular mechanics calculations Journal of the Chemical Society-Perkin Transactions 1. 1255-1259. DOI: 10.1039/P19930001255 |
0.426 |
|
| 1993 |
Gurjar M, Saha U. Synthesis of the complete glycotetrapeptide core of structurally variant glycopeptidolipid Bioorganic & Medicinal Chemistry Letters. 3: 697-702. DOI: 10.1016/S0960-894X(01)81257-9 |
0.346 |
|
| 1993 |
Gurjar MK, Mainkar AS, Syamala M. Synthesis of C- α-D-glucosyl-α-amino acids Tetrahedron-Asymmetry. 4: 2343-2346. DOI: 10.1016/S0957-4166(00)80099-3 |
0.473 |
|
| 1993 |
Rao AVR, Gurjar MK, Islam A. Synthesis of a new bicyclic guanidine heterocycle as a potential anti HIV agent Tetrahedron Letters. 34: 4993-4996. DOI: 10.1016/S0040-4039(00)74066-4 |
0.429 |
|
| 1993 |
Rao AR, Gurjar MK, Nallaganchu BR, Bhandari A. Studies on cyclodepsipeptides - part II : The total synthesis of jaspamide and geodiamolide-D Tetrahedron Letters. 34: 7085-7088. DOI: 10.1016/S0040-4039(00)61605-2 |
0.461 |
|
| 1993 |
Rao AVR, Gurjar MK, Nallaganchu BR, Bhandari A. Studies on cyclodepsipeptides - Part I : A stereoselective synthesis of C12 polyketide unit (C1–C8) present in Jaspamide and Geodiamolide A–F Tetrahedron Letters. 34: 7081-7084. DOI: 10.1016/S0040-4039(00)61604-0 |
0.466 |
|
| 1993 |
Gurjar MK, Saha UK. A stereocontrolled synthesis of the left hand (C1–C12) segment of eurylene Tetrahedron Letters. 34: 1833-1836. DOI: 10.1016/S0040-4039(00)60792-X |
0.457 |
|
| 1993 |
Gurjar MK, Kunwar AC, Reddy DV, Islam A, Lalitha SVS, Jagannadh B, Rao AVR. Syntheses and conformational studies on AZT and its deuterated analogues Tetrahedron. 49: 4373-4382. DOI: 10.1016/S0040-4020(01)85754-9 |
0.469 |
|
| 1993 |
Rao AVR, Gurjar MK, Kaiwar V, Khare VB. An expedient approach to the diphenyl ether cross-linked amino acids of glycopeptide antibiotics Tetrahedron Letters. 34: 1661-1664. DOI: 10.1016/0040-4039(93)85035-U |
0.476 |
|
| 1993 |
Rao AVR, Gurjar MK, Reddy AB, Khare VB. A new route to isodityrosine-derived cyclic peptides: Application to K-13 Tetrahedron Letters. 34: 1657-1660. DOI: 10.1016/0040-4039(93)85034-T |
0.364 |
|
| 1993 |
Rao AVR, Gurjar MK, Devi TR, Kumar KR. A formal synthesis of a novel immunosuppressant ISP-1 : Stereocontrolled Pd(O) catalysed -hydroxyamination of carbohydrate derived vinyl epoxide Tetrahedron Letters. 34: 1653-1656. DOI: 10.1016/0040-4039(93)85033-S |
0.509 |
|
| 1992 |
Gurjar MK, Reddy KR. Synthesis of methyl 2,4-di-O-methyl-3-O-(2-O-methyl-α-l-rhamnopyranosyl)-α-l-rhamnopyranoside and methyl 2,4-di-O-methyl-3-O-[2-O-methyl-3-O-(2-O-methyl-α-l-fucopyranosyl)-α-l-rhamnopyranosyl]-α-l- rhamnopyranoside: di- and tri-saccharide segments of a phenolic glycolipid of Mycobacterium kansasii Carbohydrate Research. 226: 233-238. PMID 1617686 DOI: 10.1016/0008-6215(92)84070-9 |
0.422 |
|
| 1992 |
Gurjar MK, Mainkar AS. Catalytic osmylation of allyl D-glucopyranoside Tetrahedron-Asymmetry. 3: 21-24. DOI: 10.1016/S0957-4166(00)82306-X |
0.458 |
|
| 1992 |
Rao AVR, Gurjar MK, Kaiwar V. Enantioselective catalytic reductions of ketones with new four membered oxazaborolidines: Application to (S)-tetramisole Tetrahedron-Asymmetry. 3: 859-862. DOI: 10.1016/S0957-4166(00)82184-9 |
0.466 |
|
| 1992 |
Gurjar MK, Lalitha SVS, Sharma PA, Rao AVR. First chemical synthesis of deuterated 3′-azido-3′-deoxythymidine (AZT) Tetrahedron Letters. 33: 7945-7948. DOI: 10.1016/S0040-4039(00)74785-X |
0.517 |
|
| 1992 |
Gurjar MK, Saha UK. Synthesis of a new serine containing glycotetrapeptide from Mycobacterium xenopi glycopeptidolipid : An unusual structural variant in mycobacterium genus Tetrahedron Letters. 33: 4979-4982. DOI: 10.1016/S0040-4039(00)61250-9 |
0.498 |
|
| 1992 |
Gurjar MK, Saha UK. Synthesis of the glycopeptide - O-(3,4-di-O-methyl-2-O-[3,4-di-O-methyl-α-L-rhamnopyranosyl]-α-L-rhamnopyranosyl)-L-alanilol: An unusual part structure in the glycopeptidolipid of Tetrahedron. 48: 4039-4044. DOI: 10.1016/S0040-4020(01)88483-0 |
0.456 |
|
| 1992 |
Gurjar MK, Mainkar AS. Synthesis of methyl 3-O-[3-O-(2,3,4-tri-O-methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside : The outer trisaccharide unit of a unique mycobacterium xenopi glycopeptidolipid Tetrahedron. 48: 6729-6738. DOI: 10.1016/S0040-4020(01)80018-1 |
0.443 |
|
| 1991 |
Gurjar MK, Viswanadham G. Communication: Synthesis of Me α-L-Rhap-(1↠3)-2-O-Me-α-L-Rhap And Me 2,3,4-Tri-O-Me-α-L-Fucp-(1↠3)-α-L-Rhap-(1↠3)-2-O-Me-α-L-Rhap : Oligosaccha-Ride Segments of Phenolic Glycolipids inMycobacterium Bovis BcgandTuberculosis Strain Canetti Journal of Carbohydrate Chemistry. 10: 481-485. DOI: 10.1080/07328309108543923 |
0.306 |
|
| 1991 |
Rao AVR, Gurjar MK, Bose DS, Devi RR. A simple route to (2R,3R,5E)-2-hydroxy-3-methyl-5-heptenal: a key intermediate for (4R)-4-[(E)-2-butenyl]-4,N-dimethyl-L-threonine (MeBmt) Journal of Organic Chemistry. 56: 1320-1321. DOI: 10.1021/Jo00003A078 |
0.398 |
|
| 1991 |
Gurjar MK, Srinivas NR. An ehantiospecific approach towards the C10 side-chain of bengamides Tetrahedron Letters. 32: 3409-3412. DOI: 10.1016/S0040-4039(00)92722-9 |
0.437 |
|
| 1991 |
Gurjar MK, Bhanu MN, Khare VB, Bhandari A, Deshmukh MN, Rao AVR. 1β-Methylthienamycin: Some stereocontrolled approaches towards the key intermediate Tetrahedron. 47: 7117-7128. DOI: 10.1016/S0040-4020(01)96165-4 |
0.449 |
|
| 1991 |
Gurjar MK, Viswanadham G. A stereoconvergent synthesis of the oligosaccharide segment of glyco- peptidolipid antigen of mycobacterium avium serotype 4 : a dominant serovariant observed in patients with acquired immune deficiency syndrome Tetrahedron Letters. 32: 6191-6194. DOI: 10.1016/0040-4039(91)80786-6 |
0.416 |
|
| 1991 |
Gurjar MK, Saha UK. Synthetic studies on the basic glycopeptide structure of c-mycosides Tetrahedron Letters. 32: 6621-6624. DOI: 10.1016/0040-4039(91)80238-2 |
0.436 |
|
| 1991 |
Rama Rao AV, Gurjar MK, Sharma PA. Studies directed towards the total synthesis of aranorosin Tetrahedron Letters. 32: 6613-6616. DOI: 10.1016/0040-4039(91)80236-Y |
0.47 |
|
| 1990 |
Gurjar MK, Srinivas NR. A novel synthesis of methyl 2-O-methyl-α,β-l-fucofuranoside Carbohydrate Research. 205: 398-401. PMID 2276146 DOI: 10.1016/0008-6215(90)80157-X |
0.452 |
|
| 1990 |
Gurjar MK, Mainkar PS. A formal total synthesis of (6S,7S,9R,10R)-6,9-epoxynonadec-18-ene-7,10-diol from D-glucose Heterocycles. 31: 407-410. DOI: 10.3987/Com-89-5239 |
0.478 |
|
| 1990 |
Gurjar MK. Synthesis of enantiomerically pure compounds of biological interest Pure and Applied Chemistry. 62: 1293-1298. DOI: 10.1351/pac199062071293 |
0.37 |
|
| 1990 |
Yadav JS, Mysorekar SV, Pawar SM, Gurjar MK. Synthesis of (3R, 4R)-1, 2-Divinylglycol and its Unsymmetrical Derivatives : An Application to the Synthesis of R-(+)-α-Lipoic Acid Journal of Carbohydrate Chemistry. 9: 307-316. DOI: 10.1080/07328309008543834 |
0.457 |
|
| 1990 |
Gurjar MK, Joshi SV, Sastry BS, Rama Rao AV. A New Route To (±) Metoprolol Synthetic Communications. 20: 3489-3496. DOI: 10.1080/00397919008051592 |
0.392 |
|
| 1990 |
Rama Rao AV, Gurjar MK, Khare VB, Ashok B, Deshmukh MN. Stereocontrolled approaches to the key intermediate of 1β-methylthienamycin Tetrahedron Letters. 31: 271-274. DOI: 10.1016/S0040-4039(00)94390-9 |
0.403 |
|
| 1990 |
Gurjar MK, Reddy AS. Stereoselective synthesis of (9s, 12r, 13s)-trihydroxyoctadeca(10e, 15z)dienoic acid Tetrahedron Letters. 31: 1783-1784. DOI: 10.1016/S0040-4039(00)88880-2 |
0.464 |
|
| 1990 |
Rama Rao AV, Gurjar MK, Sharma PA, Kaiwar V. Enantioselective reductions of ketones with oxazaborolidines derived from (R and (S-α-α-diphenyl-2-piperdine methanol Tetrahedron Letters. 31: 2341-2344. DOI: 10.1016/0040-4039(90)80223-9 |
0.44 |
|
| 1990 |
GURJAR MK. ChemInform Abstract: Synthesis of Enantiomerically Pure Compounds of Biological Interest Cheminform. 21. DOI: 10.1002/CHIN.199047328 |
0.388 |
|
| 1990 |
RAO AVR, DHAR TGM, BOSE DS, CHAKRABORTY TK, GURJAR MK. ChemInform Abstract: A Versatile Protocol for β-Hydroxy-α-amino Acids: An Application to (4R)-4-((E)-2-Butenyl)-4,N-dimethyl-L-threonine (MeBmt). Cheminform. 21. DOI: 10.1002/chin.199015264 |
0.563 |
|
| 1989 |
Swapna GV, Jagannadh B, Gurjar MK, Kunwar AC. NMR investigation on the structure and conformation of 3'-azido-2',3'-dideoxyribosylthymine (AZT), an inhibitor of the HIV (AIDS virus). Biochemical and Biophysical Research Communications. 164: 1086-92. PMID 2590188 DOI: 10.1016/0006-291X(89)91780-4 |
0.368 |
|
| 1989 |
Gurjar MK, Pawar SM, Mainkar PS. A Novel Strategy for 2,6-Dideoxy-L-Hexoses: An Application to 3-Amino-2,3,6-Trideoxy-L-Lyxo-Hexopyranose (L-Daunosamine) Journal of Carbohydrate Chemistry. 8: 785-791. DOI: 10.1080/07328308908048040 |
0.399 |
|
| 1989 |
Bose DS, Gurjar MK. Synthesis of (R)-(-)-γ-amino β-hydroxy Butyric Acid (GABOB) Synthetic Communications. 19: 3313-3321. DOI: 10.1080/00397918908052734 |
0.479 |
|
| 1989 |
Rao A, Dhar T, Subhas Bose D, Chakraborty T, Gurjar M. A versatile protocol for β-hydroxy-α-amino acids: an application to (4R)-4-[(e)-2-butenyl]-4n-dimethyl-l-threonine (MeBmt) Tetrahedron. 45: 7361-7370. DOI: 10.1016/S0040-4020(01)89197-3 |
0.629 |
|
| 1989 |
Rao AR, Bose DS, Gurjar MK, Ravindranathan T. 3-Butene-1,2-diol: An attractive precursor for the synthesis of enantiomerically pure organic compounds Tetrahedron. 45: 7031-7040. DOI: 10.1016/S0040-4020(01)89171-7 |
0.457 |
|
| 1989 |
Yadav JS, Krishna PR, Gurjar MK. Novel synthesis of 1,7-dihydrohept-4-yne derivatives: Application to the total synthesis of (±) patulolide A Tetrahedron. 45: 6263-6270. DOI: 10.1016/S0040-4020(01)85136-X |
0.486 |
|
| 1989 |
GURJAR MK, GHOSH PK. ChemInform Abstract: An Efficient Approach for the Synthesis of 2-Deoxy-β-D-glycosides. Cheminform. 20. DOI: 10.1002/CHIN.198923294 |
0.399 |
|
| 1988 |
Gurjar MK, Ghosh PK. methyl 2, 6-dideoxy-4-O-methyl-α-D-arabino-hexopyranoside Journal of Carbohydrate Chemistry. 7: 799-804. DOI: 10.1080/07328308808058946 |
0.363 |
|
| 1988 |
Gurjar MK, Pawar SM, Rao AVR. A Synthesis of 1,5-DI-O-Acetyl-3-Azido-2,3-Dideoxy-D-Ribofuranose Journal of Carbohydrate Chemistry. 7: 271-275. DOI: 10.1080/07328308808058920 |
0.512 |
|
| 1988 |
Rao AVR, Reddy KA, Gurjar MK, Kunwar AC. Radical dideoxygenation reaction of a 1,4-bis-dithiocarbonate: a strategy for the synthesis of chiral polyhydroxylated thiolane derivatives Journal of the Chemical Society, Chemical Communications. 1273-1274. DOI: 10.1039/C39880001273 |
0.487 |
|
| 1988 |
Rao A, Dhar T, Chakraborty T, Gurjar M. A stereospecific synthesis of (4R)-4-[(E)-2-butenyl]-4, N-dimethyl-L-threonine (MeBmt) Tetrahedron Letters. 29: 2069-2072. DOI: 10.1016/S0040-4039(00)87837-5 |
0.635 |
|
| 1988 |
GURJAR MK, PURANDARE AV. ChemInform Abstract: An Efficient Route for γ-Alkyl-γ-butyrolactones. Cheminform. 19. DOI: 10.1002/chin.198847150 |
0.354 |
|
| 1988 |
GURJAR MK, PATIL VJ, PAWAR SM. ChemInform Abstract: Synthesis of N-Acetyl Derivatives of (1R,5R)-6-Aza-2-oxabicyclo(3.3.0)octan-3-one and (1S,5R,8R)-8-O-Benzyl-6-aza-2-oxabicyclo(3.3.0)octan-3-one from D-Glucose. Cheminform. 19. DOI: 10.1002/CHIN.198826323 |
0.325 |
|
| 1988 |
GURJAR MK, PATIL VJ, PAWAR SM. ChemInform Abstract: L-Daunosamine: Its Synthesis from Carbohydrate Precursors Cheminform. 19. DOI: 10.1002/CHIN.198814384 |
0.378 |
|
| 1987 |
Rao AVR, Purandare AV, Reddy ER, Gurjar MK. Synthesis of R(+)-α-lipoic acid Synthetic Communications. 17: 1095-1102. DOI: 10.1080/00397918708078791 |
0.488 |
|
| 1987 |
Rao AVR, Mysorekar SV, Gurjar MK, Yadav JS. Synthesis of (3R,4R)-1,5-hexadien-3,4-diol and its unsymmetricalderivatives: application to (R)-(+)-∝-lipoic acid Tetrahedron Letters. 28: 2183-2186. DOI: 10.1016/S0040-4039(00)96076-3 |
0.419 |
|
| 1987 |
Gurjar M, Pawar S. Synthesis of L-daunosamine from D-glucurono-6,3-lactone Tetrahedron Letters. 28: 1327-1328. DOI: 10.1016/S0040-4039(00)95361-9 |
0.364 |
|
| 1987 |
Gurjar MK, Pawar SM. Synthesis of some derivatives of 2-O-allyl-d-glucose Carbohydrate Research. 159: 325-327. DOI: 10.1016/S0008-6215(00)90225-8 |
0.459 |
|
| 1987 |
Gurjar MK, Patil VJ, Pawar SM. Synthesis of (1R,5R)-2,6-dioxabicyclo[3.3.0]octan-3-one from d-glucose Carbohydrate Research. 165: 313-317. DOI: 10.1016/0008-6215(87)80108-8 |
0.412 |
|
| 1987 |
Yadav JS, Joshi BV, Gurjar MK. An enantiospecific synthesis of (4R,5R)-5-hydroxy-4-decanolide from D-glucose Carbohydrate Research. 165: 116-119. DOI: 10.1016/0008-6215(87)80084-8 |
0.419 |
|
| 1987 |
GURJAR MK, DHAR TGM. ChemInform Abstract: Novel Synthesis of Hex-2-enopyranosides. Cheminform. 18. DOI: 10.1002/CHIN.198751335 |
0.475 |
|
| 1987 |
GURJAR MK, PAWAR SM. ChemInform Abstract: Synthesis of L-Daunosamine (II) from D-Glucurono-6,3-lactone (I). Cheminform. 18. DOI: 10.1002/CHIN.198735336 |
0.353 |
|
| 1987 |
GURJAR MK, PAWAR SM. ChemInform Abstract: A Simple Synthesis of R,R-3,4-Dibenzyloxy-threo-hexa-1,5-diene (R,R-Divinylglycol) from D-Mannitol. Cheminform. 18. DOI: 10.1002/CHIN.198730159 |
0.295 |
|
| 1987 |
GURJAR MK, PATIL VJ. ChemInform Abstract: Synthesis of 3-Acetamido- and 3-Azido-3-deoxy-1,2-O-isopropylidene-α-D-xylohexofuran-5-ulose. Cheminform. 18. DOI: 10.1002/chin.198717334 |
0.401 |
|
| 1987 |
GURJAR MK, HOUGH L, RICHARDSON AC, SINCHAROENKUL LV. ChemInform Abstract: Sucrochemistry. Part 36. Preparation and Ring-Opening Reactions of a 2,3-Anhydride Derived from Sucrose. Cheminform. 18. DOI: 10.1002/CHIN.198712351 |
0.388 |
|
| 1986 |
Rama Rao AV, Gurjar MK, Garyali K, Ravindranathan T. Enantiospecific synthesis of (R-(+)-α-lipoic acid from d-glucose Carbohydrate Research. 148: 51-55. DOI: 10.1016/0008-6215(86)80035-0 |
0.488 |
|
| 1986 |
Gurjar MK, Hough L, Richardson AC, Sincharoenkul LV. Preparation and ring-opening reactions of a 2,3-anhydride derived from sucrose Carbohydrate Research. 150: 53-61. DOI: 10.1016/0008-6215(86)80005-2 |
0.421 |
|
| 1986 |
Rao AVR, Gurjar MK, Garyali K, Ravindranathan T. Enantiospecific Synthesis of (R)-(+)-α-Lipoic Acid from D-Glucose. Cheminform. 17. DOI: 10.1002/Chin.198652160 |
0.468 |
|
| 1986 |
GURJAR MK, PATIL VJ. ChemInform Abstract: Synthesis of (S)-Hydroxyethyl-y-butyrolactone and Its Application to the Synthesis of R(+)-γ-Caprolactone. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198644335 |
0.432 |
|
| 1986 |
GURJAR MK, PATIL VJ. ChemInform Abstract: Synthesis of N-Acetyl-(1R,5R)-6-aza-2-oxabicyclo[3.3.0]octan-3-one. Chemischer Informationsdienst. 17. DOI: 10.1002/CHIN.198620325 |
0.316 |
|
| 1985 |
Aspinall GO, Gurjar MK. 8-Methoxycarbonyloctyl 2-O-α-d-glucopyranosyl-α-d-glucopyranoside Carbohydrate Research. 143: 266-270. DOI: 10.1016/S0008-6215(00)90718-3 |
0.311 |
|
| 1985 |
Gurjar MK, Patil VJ, Yadav JS, Rao AVR. METHYL 3-BENZAMIDO-4-O-BENZOYL-2,3,6-TRIDEOXY-2-FLUORO-β-L-GALACTOPYRANOSIDE Cheminform. 16. DOI: 10.1002/Chin.198523330 |
0.394 |
|
| 1984 |
Gurjar MK, Patil VJ, Yadav JS, Rao AVR. Synthesis of methyl 3-N-benzoyl-4-O-benzoyl-β-l-daunosaminide☆ Carbohydrate Research. 129: 267-270. DOI: 10.1016/0008-6215(84)85317-3 |
0.442 |
|
| 1984 |
Gurjar MK, Patil VJ, Yadav JS, Rao AVR. Methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-2-fluoro-β-l-galactopyranoside Carbohydrate Research. 135: 174-177. DOI: 10.1016/0008-6215(84)85015-6 |
0.432 |
|
| 1984 |
Gurjar MK, Patil VJ, Yadav JS, Rao AVR. SYNTHESIS OF METHYL 3-N-BENZOYL-4-O-BENZOYL-β-L-DAUNOSAMINIDE Cheminform. 15. DOI: 10.1002/Chin.198451325 |
0.442 |
|
| 1984 |
GURJAR MK, YADAV JS, RAO AVR. ChemInform Abstract: SYNTHESIS OF L-DAUNOSAMINE Chemischer Informationsdienst. 15. DOI: 10.1002/CHIN.198426329 |
0.362 |
|
| 1982 |
Chiu AKB, Gurjar MK, Hough L, Sincharoenkul LV, Richardson AC. The synthesis of 2,1′-anhydro-,2,1′:3,6-dianhydro-, and 2,1′:3,6: 3′,6′-trianhydro-sucrose Carbohydrate Research. 100: 247-261. DOI: 10.1016/S0008-6215(00)81039-3 |
0.378 |
|
| 1982 |
Chiu AKB, Gurjar MK, Hough L, Sincharoenkul LV, Richardson AC. The Synthesis of 2,1′-Anhydro-, 2,1′:3,6-Dianhydro-, and 2,1′:3,6:3′,6′-Trianhydro-sucrose. Sucrochemistry. Part 32. Cheminform. 13. DOI: 10.1002/Chin.198238348 |
0.378 |
|
| 1980 |
Gurjar MK, Hough L, Richardson AC. The formation of a 2,1′-anhydro linkage in sucrose Carbohydrate Research. 78: C21-C23. DOI: 10.1016/0008-6215(80)90019-1 |
0.293 |
|
| 1976 |
GURJAR MK, BAGAVANT G. ChemInform Abstract: CLAISEN STOBBE REACTION OF ETHYL β-NAPHTHOXYACETATE AND AROMATIC ALDEHYDES Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/CHIN.197646126 |
0.34 |
|
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