| Year |
Citation |
Score |
| 2019 |
Sarkar D, Bera N, Ghosh S. [2+2] Photochemical Cycloaddition in Organic Synthesis European Journal of Organic Chemistry. 2020: 1310-1326. DOI: 10.1002/Ejoc.201901143 |
0.356 |
|
| 2018 |
Datta R, Ghosh S. Domino ring-opening-ring-closing enyne metathesis vs enyne metathesis of norbornene derivatives with alkynyl side chains. Construction of condensed polycarbocycles. Beilstein Journal of Organic Chemistry. 14: 2708-2714. PMID 30410632 DOI: 10.3762/Bjoc.14.248 |
0.387 |
|
| 2017 |
Datta R, Ghosh S. Total synthesis of the marine polyketide (-)-gracilioether F. The Journal of Organic Chemistry. PMID 28636373 DOI: 10.1021/Acs.Joc.7B01179 |
0.38 |
|
| 2017 |
Datta R, Ghosh S. Influence of alkene substituent in dictating the reaction course to form carbocycles or oxacycles during ring closing metathesis of acyclic trienes Journal of Chemical Sciences. 129: 1873-1881. DOI: 10.1007/S12039-017-1390-3 |
0.372 |
|
| 2016 |
Datta R, Dixon RJ, Ghosh S. A convenient access to the tricyclic core structure of hippolachnin A Tetrahedron Letters. 57: 29-31. DOI: 10.1016/J.Tetlet.2015.11.045 |
0.4 |
|
| 2016 |
Datta R, Sumalatha M, Ghosh S. A simple approach to the construction of the core structure present in bielschowskysin and hippolachnin A Journal of Chemical Sciences. 128: 1019-1023. DOI: 10.1007/S12039-016-1109-X |
0.433 |
|
| 2015 |
Jana A, Mondal S, Ghosh S. Studies towards the synthesis of bielschowskysin. Construction of the highly functionalized bicyclo[3.2.0]heptane segment. Organic & Biomolecular Chemistry. 13: 1846-59. PMID 25502963 DOI: 10.1039/C4Ob02182G |
0.436 |
|
| 2015 |
Ganguly B, Chakraborty I, Ghosh S, Chandar N, Sarkar D, Ghosh M. Unprecedented C-Methylation at the 2-Position of 2-Carboxy- 4-Chromanones – A Case Study with the Corey–Chaykovsky Reagent Synlett. 26: 2472-2472. DOI: 10.1055/S-0035-1560799 |
0.327 |
|
| 2014 |
Ghosh S, Bose S, Jana A, Nijamudheen A, Datta A. Influence of ring fusion stereochemistry on the stereochemical outcome in photo-induced Diels–Alder reaction of fused bicycloheptenone derivatives Tetrahedron. 70: 9783-9790. DOI: 10.1016/J.Tet.2014.11.025 |
0.39 |
|
| 2014 |
Ghosh A, Ghosh S. Asymmetric synthesis of a functionalized tricyclo[6.2.0.02,6]decane ring system present in kelsoene and poduran Journal of Chemical Sciences. 126: 1875-1882. DOI: 10.1007/S12039-014-0739-0 |
0.483 |
|
| 2013 |
Hossain MF, Yadav RN, Mondal S, Jana A, Ghosh S. Intramolecular Diels–Alder route to angularly oxygenated hydrindanes. Synthesis of the functionalized bicylic skeleton present in galiellalactone Tetrahedron. 69: 7956-7963. DOI: 10.1016/J.Tet.2013.07.014 |
0.396 |
|
| 2012 |
Bose S, Ghosh M, Ghosh S. Domino ring-opening metathesis-ring-closing metathesis of bicyclo[2.2.2]octene derivatives: scope and limitations. The Journal of Organic Chemistry. 77: 6345-50. PMID 22731765 DOI: 10.1021/Jo300945B |
0.387 |
|
| 2012 |
Jana A, Mondal S, Firoj Hossain M, Ghosh S. Stereocontrolled approach to the highly functionalized bicyclo[3.2.0] heptane core of bielschowskysin through intramolecular Cu(I)-catalyzed [2+2] photocycloaddition Tetrahedron Letters. 53: 6830-6833. DOI: 10.1016/J.Tetlet.2012.10.018 |
0.427 |
|
| 2011 |
Mondal S, Yadav RN, Ghosh S. Influence of diene substituent position on the stereochemical outcome in IMDA reaction of decatrienones. An asymmetric synthesis of C10-epi-dihydro-epi-deoxy arteannuin B. Organic Letters. 13: 6078-81. PMID 22014357 DOI: 10.1021/Ol202562W |
0.393 |
|
| 2011 |
Mondal S, Yadav RN, Ghosh S. Unprecedented influence of remote substituents on reactivity and stereoselectivity in Cu(I)-catalysed [2 + 2] photocycloaddition. An approach towards the synthesis of tricycloclavulone. Organic & Biomolecular Chemistry. 9: 4903-13. PMID 21573291 DOI: 10.1039/C1Ob05233K |
0.453 |
|
| 2011 |
Firoj Hossain M, Matcha K, Ghosh S. Synthetic studies toward nortriterpenoids of schisandraceae family. Approach to the construction of functionalized C/D and A/B ring units of micrandilactone C and rubrifloradilactone B Tetrahedron Letters. 52: 6473-6476. DOI: 10.1016/J.Tetlet.2011.09.104 |
0.331 |
|
| 2011 |
Yadav RN, Mondal S, Ghosh S. An efficient stereoselective route to the construction of tricyclic core structure towards the synthesis of the sesquiterpenes of the seco-prezizaane family Tetrahedron Letters. 52: 1942-1945. DOI: 10.1016/J.Tetlet.2011.02.054 |
0.394 |
|
| 2010 |
Maity S, Matcha K, Ghosh S. Synthetic studies on schisandra nortriterpenoids. Stereocontrolled synthesis of enantiopure C-5-epi ABC ring systems of micrandilactone A and lancifodilactone G using RCM. The Journal of Organic Chemistry. 75: 4192-200. PMID 20491457 DOI: 10.1021/Jo1006448 |
0.662 |
|
| 2010 |
Matcha K, Ghosh S. An asymmetric route to total synthesis of the furano lignan (+)-veraguensin Tetrahedron Letters. 51: 6924-6927. DOI: 10.1016/J.Tetlet.2010.10.136 |
0.468 |
|
| 2010 |
Mondal S, Yadav RN, Ghosh S. Unprecedented copper(I)-catalyzed photochemical reaction of diethyl ether with vicinal diols and ketals Tetrahedron Letters. 51: 4452-4454. DOI: 10.1016/J.Tetlet.2010.06.080 |
0.401 |
|
| 2010 |
Matcha K, Maity S, Malik CK, Ghosh S. Expedient route to CDE ring system of schintrilactones through tandem ROM–RCM of a norbornene derivative Tetrahedron Letters. 51: 2754-2757. DOI: 10.1016/J.Tetlet.2010.03.074 |
0.661 |
|
| 2010 |
Ghosh S, Hossain MF, Malik CK, Maity S. Effect of ring fusion stereochemistry on double bond geometry. Unexpected formation of nine-membered cyclic ether with E-configurated double bond through RCM Tetrahedron. 66: 9159-9164. DOI: 10.1016/J.Tet.2010.09.084 |
0.596 |
|
| 2010 |
Maity S, Ghosh S. An asymmetric route to 2,3-epoxy-syn-1,4-cyclohexane diol derivatives using ring closing metathesis (RCM) Journal of Chemical Sciences. 122: 791-800. DOI: 10.1007/S12039-010-0066-Z |
0.683 |
|
| 2010 |
Ghatak A, Ghosh S. ChemInform Abstract: Synthesis of 8-(3′-Butenyl)-9,9-dimethyl-2-oxaspiro[4.4]non-7-en-1-one, an Advanced Intermediate for Terpenes of the Marine Sponge Dysidea herbacea. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199940163 |
0.312 |
|
| 2010 |
Haque A, Panda J, Ghosh S. ChemInform Abstract: Facile Annulation of Six-Membered Ether Rings on to Carbohydrate Template Based on Ring Closing Metathesis. Synthesis of Enantiopure Bicyclic Ethers. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199928169 |
0.309 |
|
| 2010 |
SALOMON RG, GHOSH S, RAYCHAUDHURI S. ChemInform Abstract: Homogeneous Metal-Catalyzed Photochemistry in Organic Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199445304 |
0.485 |
|
| 2009 |
Malik CK, Yadav RN, Drew MG, Ghosh S. Synthesis of fused cyclic systems containing medium-sized rings through tandem ROM-RCM of norbornene derivatives embedded in a carbohydrate template. The Journal of Organic Chemistry. 74: 1957-63. PMID 19191710 DOI: 10.1021/Jo802077T |
0.361 |
|
| 2009 |
Ghosh M, Bose S, Maity S, Ghosh S. Enantiodivergent synthesis of (−)-methylenolactocin and (+)-methylenolactocin from d-mannitol Tetrahedron Letters. 50: 7102-7104. DOI: 10.1016/J.Tetlet.2009.10.011 |
0.649 |
|
| 2009 |
Mondal S, Yadav RN, Ghosh S. Expedient asymmetric synthesis of a functionalized 5-7-6 fused tricyclic skeleton present in caribenol A through ring opening-ring closing metathesis of a norbornene derivative Tetrahedron Letters. 50: 5277-5279. DOI: 10.1016/J.Tetlet.2009.07.012 |
0.426 |
|
| 2009 |
Malik CK, Hossain MF, Ghosh S. A new approach to A/B ring analogue of eleutherobin and sarcodictyns through a sequence of highly diastereofaceselective Diels–Alder reaction and ring opening–ring closing metathesis (RO–RCM) Tetrahedron Letters. 50: 3063-3066. DOI: 10.1016/J.Tetlet.2009.04.033 |
0.39 |
|
| 2009 |
Maity S, Ghosh S. A direct route to angularly substituted hydrindanes. Formal synthesis of bakkenolide-A and synthesis of an advanced intermediate to umbellactal Tetrahedron. 65: 9202-9210. DOI: 10.1016/J.Endend.2010.01.013 |
0.684 |
|
| 2009 |
Nandakumar MV, Ghosh S, Schneider C. Enantioselective Synthesis of a Novel Chiral 2,9-Disubstituted 1,10-Phenanthroline and First Applications in Asymmetric Catalysis European Journal of Organic Chemistry. 2009: 6393-6398. DOI: 10.1002/Ejoc.200901038 |
0.366 |
|
| 2008 |
Mondal S, Malik CK, Ghosh S. A novel asymmetric approach to a densely functionalized lactarane ring system through a domino ring opening–ring closing metathesis of a norbornene derivative Tetrahedron Letters. 49: 5649-5651. DOI: 10.1016/J.Tetlet.2008.07.083 |
0.443 |
|
| 2008 |
Ghosh M, Bose S, Ghosh S. A simple route to the syntheses of both enantiomers of trans-oak lactone and (+)-cis-oak lactone Tetrahedron Letters. 49: 5424-5426. DOI: 10.1016/J.Tetlet.2008.07.026 |
0.333 |
|
| 2008 |
Matcha K, Ghosh S. A stereocontrolled approach for the synthesis of 2,5-diaryl-3,4-disubstituted furano lignans through a highly diastereoselective aldol condensation of an ester enolate with an α-chiral center: total syntheses of (−)-talaumidin and (−)-virgatusin Tetrahedron Letters. 49: 3433-3436. DOI: 10.1016/J.Tetlet.2008.03.105 |
0.417 |
|
| 2008 |
Maity S, Ghosh S. Rapid assembly of the functionalized tricyclic core of umbellactal through domino metathesis involving ROM-RCM of a norbornene derivative Tetrahedron Letters. 49: 1133-1136. DOI: 10.1016/J.Tetlet.2007.12.064 |
0.616 |
|
| 2008 |
Mondal S, Ghosh S. A simple route to enantiopure bis-lactones: synthesis of both enantiomers of epi-nor-canadensolide, nor-canadensolide, and canadensolide Tetrahedron. 64: 2359-2368. DOI: 10.1016/J.Tet.2008.01.009 |
0.43 |
|
| 2007 |
Malik CK, Ghosh S. Domino metathesis involving ROM-RCM of substituted norbornenes. Rapid access to densely functionalized tricyclic bridged and condensed ring systems. Organic Letters. 9: 2537-40. PMID 17536812 DOI: 10.1021/Ol070906A |
0.359 |
|
| 2007 |
Malik CK, Vaultier M, Ghosh S. Copper(I)-catalyzed [2+2] photocycloaddition of nonconjugated alkenes in room-temperature ionic liquids. Synthesis. 2007: 1247-1250. DOI: 10.1055/S-2007-965971 |
0.32 |
|
| 2007 |
Maity S, Ghosh S. The first total synthesis of sequosempervirin A through an orthoester Claisen rearrangement—ring closing metathesis sequence Tetrahedron Letters. 48: 3355-3358. DOI: 10.1016/J.Tetlet.2007.03.084 |
0.631 |
|
| 2007 |
Sarkar N, Ghosh S. Asymmetric Induction in Copper(I)-Catalyzed Intramolecular [2 + 2] Photocycloaddition: Synthesis of Enantiopure Cyclobutane Derivatives. Cheminform. 38. DOI: 10.1002/CHIN.200710030 |
0.406 |
|
| 2006 |
Ghosh S, Bhaumik T, Sarkar N, Nayek A. A convenient approach for access to both carbapentofuranoses and carbahexopyranoses. Stereocontrolled synthesis of enantiopure carba-D-ribofuranoses, carba-D-arabinofuranoses and carba-L-gulopyranose. The Journal of Organic Chemistry. 71: 9687-94. PMID 17168586 DOI: 10.1021/Jo061717T |
0.773 |
|
| 2006 |
Ghosh S, Sinha S, Drew MG. Stereodivergent approach to the asymmetric synthesis of bacillariolides: a formal synthesis of ent-bacillariolide II. Organic Letters. 8: 3781-4. PMID 16898816 DOI: 10.1021/Ol061377Y |
0.453 |
|
| 2006 |
Banerjee S, Nayek A, Sinha S, Bhaumik T, Ghosh S. Alkoxy group facilitated ring closing metathesis (RCM) of acyclic 1,6-dienes Journal of Molecular Catalysis a: Chemical. 254: 85-92. DOI: 10.1016/J.Molcata.2006.03.023 |
0.4 |
|
| 2006 |
Ghosh S, Ghosh S, Sarkar N. Factors influencing ring closure through olefin metathesis – A perspective Journal of Chemical Sciences. 118: 223-235. DOI: 10.1007/Bf02708281 |
0.358 |
|
| 2005 |
Banerjee S, Ghosh S, Sinha S, Ghosh S. Convenient route to both enantiomers of a highly functionalized trans-disubstituted cyclopentene. Synthesis of the carbocyclic core of the nucleoside BCA. The Journal of Organic Chemistry. 70: 4199-202. PMID 15876120 DOI: 10.1021/Jo0502504 |
0.44 |
|
| 2005 |
Sarkar N, Nayek A, Ghosh S. Copper(I)-catalyzed intramolecular asymmetric [2 + 2] photocycloaddition. Synthesis of both enantiomers of cyclobutane derivatives. Organic Letters. 6: 1903-5. PMID 15176779 DOI: 10.1021/Ol049696H |
0.446 |
|
| 2004 |
Holt DJ, Barker WD, Ghosh S, Jenkins PR. The synthesis of fused and spiro annulated carbohydrate structures using copper(I) catalysed intramolecular photoannulation of glucose derivatives. Organic & Biomolecular Chemistry. 2: 1093-7. PMID 15034635 DOI: 10.1039/B315623K |
0.336 |
|
| 2004 |
Sinha S, Bhaumik T, Ghosh S. An asymmetric route to the construction of the bicyclic framework of marine eicosanoids Bacillariolides Arkivoc. 2005. DOI: 10.3998/Ark.5550190.0006.B04 |
0.438 |
|
| 2004 |
Nayek A, Banerjee S, Sinha S, Ghosh S. Alkoxy group facilitated ring closing metathesis (RCM) of acyclic 1,6-dienes. Convenient synthesis of non-racemic highly substituted cyclopentenols Tetrahedron Letters. 45: 6457-6460. DOI: 10.1016/J.Tetlet.2004.06.127 |
0.443 |
|
| 2003 |
Banerjee S, Ghosh S. Intramolecular [2 + 2] photocycloaddition of alkenes incorporated in a carbohydrate template. Synthesis of enantiopure bicyclo[3.2.0]heptanes and -[6.3.0]undecanes. The Journal of Organic Chemistry. 68: 3981-9. PMID 12737581 DOI: 10.1021/Jo026920C |
0.408 |
|
| 2003 |
Nayek A, Drew MG, Ghosh S. Convenient route to enantiopure aryl cyclopentanes via Diels–Alder reaction of asymmetric dienes. Total synthesis of (+)-herbertene and (+)-cuparene Tetrahedron. 59: 5175-5181. DOI: 10.1016/S0040-4020(03)00807-X |
0.48 |
|
| 2003 |
Salomon RG, Ghosh S. Copper(I)‐Catalyzed Photocycloaddition: 3,3‐Dimethyl‐cis‐bicyclo[3.2.0]heptan‐2‐one Organic Syntheses. 125-125. DOI: 10.1002/0471264180.Os062.16 |
0.572 |
|
| 2002 |
Ghosh S, Banerjee S. Carbon-carbon bond cleavage in norbornane derivatives. Convenient route to novel carbocyclic rings Arkivoc. 2002. DOI: 10.3998/Ark.5550190.0003.702 |
0.385 |
|
| 2002 |
Nayek A, Ghosh S. Enantiospecific synthesis of (+)-herbertene Tetrahedron Letters. 43: 1313-1315. DOI: 10.1016/S0040-4039(01)02365-6 |
0.45 |
|
| 2001 |
Panda J, Ghosh S, Ghosh S. Synthesis of cyclobutane fused γ-butyro lactones through intramolecular [2+2] photocycloaddition. Application in a formal synthesis of grandisol Arkivoc. 2001. DOI: 10.3998/Ark.5550190.0002.816 |
0.479 |
|
| 2001 |
Panda J, Ghosh S, Ghosh S. A new stereoselective route to the carbocyclic nucleoside cyclobut-A Journal of the Chemical Society-Perkin Transactions 1. 3013-3016. DOI: 10.1039/B106542B |
0.453 |
|
| 2001 |
Ghosh S, Banerjee S, Chowdhury K, Mukherjee M, Howard JA. Intramolecular [2+2] photocycloaddition of 1,6-dienes incorporated in a furanose ring. Unusual formation of cis-syn-cis 6-oxatricyclo[6.2.0.03,7]decanes Tetrahedron Letters. 42: 5997-6000. DOI: 10.1016/S0040-4039(01)01167-4 |
0.338 |
|
| 2001 |
Samajdar S, Ghatak A, Banerjee S, Ghosh S. High diastereoselectivity in Claisen rearrangement in a sterically congested cyclopentane system. Total synthesis of (±)-β-necrodol Tetrahedron. 57: 2011-2014. DOI: 10.1016/S0040-4020(01)00019-9 |
0.38 |
|
| 2000 |
Holt DJ, Barker WD, Jenkins PR, Panda J, Ghosh S. Stereoselective preparation of enantiomerically pure annulated carbohydrates using ring-closing metathesis Journal of Organic Chemistry. 65: 482-493. DOI: 10.1021/Jo991392Z |
0.383 |
|
| 1999 |
Panda J, Ghosh S. Intramolecular [2+2] photocycloaddition for the direct stereoselective synthesis of cyclobutane fused γ-lactols Tetrahedron Letters. 40: 6693-6694. DOI: 10.1016/S0040-4039(99)01379-9 |
0.464 |
|
| 1999 |
Samajdar S, Ghatak A, Ghosh S. Stereocontrolled total synthesis of (±)-β-necrodol Tetrahedron Letters. 40: 4401-4402. DOI: 10.1016/S0040-4039(99)00737-6 |
0.395 |
|
| 1998 |
Samajdar S, Patra D, Ghosh S. Stereocontrolled approach to highly substituted cyclopentanones. Application in a formal synthesis of Δ9(12)-capnellene Tetrahedron. 54: 1789-1800. DOI: 10.1016/S0040-4020(97)10387-8 |
0.391 |
|
| 1997 |
Haque A, Ghatak A, Ghosh S, Ghoshal N. A facile access to densely functionalized substituted cyclopentanes and spiro cyclopentanes. Carbocation stabilization directed bond migration in rearrangement of cyclobutanes Journal of Organic Chemistry. 62: 5211-5214. DOI: 10.1021/Jo970283M |
0.399 |
|
| 1997 |
Ghatak A, Sarkar S, Ghosh S. Strategic use of retro Diels-Alder reaction in the construction of β-carboxy-α-methylene-γ-lactones. Total synthesis of methylenolactocin and protolichesterinic acid Tetrahedron. 53: 17335-17342. DOI: 10.1016/S0040-4020(97)10157-0 |
0.378 |
|
| 1996 |
Ghosh S, Patra D. Synthesis of cyclopentanoids - a never ending challenge Pure and Applied Chemistry. 68: 597-600. DOI: 10.1351/Pac199668030597 |
0.426 |
|
| 1996 |
Sarkar S, Ghosh S. A short synthesis of (±) - methylenolactocin Tetrahedron Letters. 37: 4809-4810. DOI: 10.1016/0040-4039(96)00942-2 |
0.41 |
|
| 1996 |
Ghosh S, Patra D, Samajdar S. Intramolecular [2+2] photocycloaddition — cyclobutane rearrangement. A novel stereocontrolled approach to highly substituted cyclopentanones Tetrahedron Letters. 37: 2073-2076. DOI: 10.1016/0040-4039(96)00195-5 |
0.457 |
|
| 1995 |
Sarkar S, Ghosh S. Reaction of bis-Lactone in Rigid Polycycles with Alkyl Lithiums. Synthesis of Novel Oxa-Cace Compounds Synthetic Communications. 25: 3723-3728. DOI: 10.1080/00397919508011445 |
0.379 |
|
| 1995 |
Sarkar S, Ghosh S. Synthesis of Methyl-6-methyl Tricyclo[5.2.1.02,6]decan-9-one-2-carboxylate: Potential Intermediate to Isocomene and Cuprenolide Synthetic Communications. 25: 3713-3722. DOI: 10.1080/00397919508011444 |
0.34 |
|
| 1995 |
Patra D, Ghosh S. Photocycloaddition-cyclobutane rearrangement to spiro cyclopentanones: application in a formal synthesis of (±)-α-cedrene Journal of the Chemical Society-Perkin Transactions 1. 2635-2641. DOI: 10.1039/P19950002635 |
0.496 |
|
| 1995 |
Patra D, Ghosh S. Regioselectivity and Stereospecificity in a Contrastereoelectronically Controlled Pinacol Rearrangement of Alkoxycyclobutane Derivatives. A Novel Route to Vicinally Substituted Cyclopentanones Journal of Organic Chemistry. 60: 2526-2531. DOI: 10.1021/Jo00113A036 |
0.386 |
|
| 1994 |
Sarkar S, Ghosh S. Carbon-carbon bond cleavage via carbon centred radical in strained tricyclo[5.2.1.02,6]decenes. A facile route to bridged eight membered rings related to taxanes Tetrahedron. 50: 921-930. DOI: 10.1016/S0040-4020(01)80806-1 |
0.312 |
|
| 1993 |
Ghosh S, Sarkar S, Saha G. Strain-assisted reductive ring cleavage: convenient route to bridged eight-membered rings present in taxanes Journal of the Chemical Society-Perkin Transactions 1. 2281-2286. DOI: 10.1039/P19930002281 |
0.345 |
|
| 1993 |
Ghosh S, Patra D, Saha G. A novel route to usefully functionalised spiro[n.4] systems; Application to a formal synthesis of (±)-α-cedrene Journal of the Chemical Society, Chemical Communications. 783-784. DOI: 10.1039/C39930000783 |
0.361 |
|
| 1993 |
Sarkar S, Ghosh S. Strain assisted carbon-carbon bond cleavage via carbon centred radical. A facile route to bridged eight membered rings Tetrahedron Letters. 34: 2987-2988. DOI: 10.1016/S0040-4039(00)60501-4 |
0.305 |
|
| 1993 |
Ghosh S, Patra D. A convenient route to vicinally substituted cyclopentanones via pinacol type rearrangement of cyclobutanes Tetrahedron Letters. 34: 4565-4566. DOI: 10.1016/0040-4039(93)88087-Y |
0.434 |
|
| 1992 |
Saha G, Karpha A, Roy SS, Ghosh S. A simple approach to the bicyclo[5.3.1]undecane system present in taxanes Journal of the Chemical Society-Perkin Transactions 1. 1587-1591. DOI: 10.1039/P19920001587 |
0.453 |
|
| 1992 |
Ghosh S, Saha G, Mostafa G, Ray S. Halogen-assisted alkylation of ester enolates. Facile synthesis of C10-functionalized tricyclo[5.2.1.02,6]decenes Journal of Organic Chemistry. 57: 7344-7346. DOI: 10.1021/Jo00052A062 |
0.406 |
|
| 1992 |
Sarkar S, Saha G, Ghosh S. Exclusive peri-selective and regio- and stereoselective cycloaddition reactions of benzocycloheptadienones Journal of Organic Chemistry. 57: 5771-5773. DOI: 10.1021/Jo00047A038 |
0.318 |
|
| 1991 |
Saha G, Ghosh S. A New Route to the Synthesis of 7-Functionalised Bicyclo[2.2.1 ]Heptane Derivatives Synthetic Communications. 21: 2129-2136. DOI: 10.1080/00397919108055445 |
0.369 |
|
| 1990 |
Saha G, Bhattacharya A, Saha Roy S, Ghosh S. A simple approach to the construction of bicyclo[5.2.1] and [5.3.1] ring systems from bicyclo[2.2.1]Heptane precursors Tetrahedron Letters. 31: 1483-1484. DOI: 10.1016/S0040-4039(00)88838-3 |
0.358 |
|
| 1990 |
Saha G, Saha Roy S, Ghosh S. Biyclo[2.2.1]heptane as cyclopentane precursor. Part 41 Stereocontrolled syhthesis of a potential intermediate to chromophycane dolastane and clavularane Tetrahedron. 46: 8229-8236. DOI: 10.1016/S0040-4020(01)81478-2 |
0.451 |
|
| 1989 |
Iyer RS, Ghosh S, Salomon RG. Levuglandin E2 crosslinks proteins Prostaglandins. 37: 471-480. PMID 2762557 DOI: 10.1016/0090-6980(89)90096-8 |
0.456 |
|
| 1989 |
Ghosh S, Roy SS, Bhattacharya A. Bicyclo[2.2.1]Heptane as Cyclopentane Precursor. Part 31. A Convenient Route to [3.3.3]Propellanes Synthetic Communications. 19: 3191-3197. DOI: 10.1080/00397918908052719 |
0.377 |
|
| 1988 |
Ghosh S, Saha Roy S, Saha G. An expeditious route to trans fused 5-7-6 and 6-7-6 carbocycles through photoisomerisation-cycloaddition of benzocycloheptenone Tetrahedron. 44: 6235-6240. DOI: 10.1016/S0040-4020(01)89814-8 |
0.351 |
|
| 1988 |
ROY SS, GHOSH S. ChemInform Abstract: Bicyclo(2.2.1)heptane as Cyclopentane Precursor. Synthesis of Benzhydropentalenes en Route to Terpenoids. Cheminform. 19. DOI: 10.1002/chin.198815332 |
0.346 |
|
| 1987 |
Salomon RG, Jirousek MR, Ghosh S, Sharma RB. Prostaglandin endoperoxidase 21. Covalent binding of levuglandin E2 with proteins Prostaglandins. 34: 643-656. PMID 3481092 DOI: 10.1016/0090-6980(87)90289-9 |
0.684 |
|
| 1987 |
Lal K, Ghosh S, Salomon RG. Hydroxyl-directed regioselective monodemethylation of polymethoxyarenes Journal of Organic Chemistry. 52: 1072-1078. DOI: 10.1021/Jo00382A018 |
0.689 |
|
| 1987 |
Ghosh S, Raychaudhuri SR, Salomon RG. Copper(I) catalysis of olefin photoreactions. 15. Synthesis of cyclobutanated butyrolactones via copper(I)-catalyzed intermolecular photocycloadditions of homoallyl vinyl or diallyl ethers The Journal of Organic Chemistry. 52: 83-90. DOI: 10.1021/Jo00377A015 |
0.79 |
|
| 1987 |
Saha Roy (nee Saha) S, Ghosh S. Bicyclo [2.2.1]heptane as cyclopentane precursor. synthesis of benzhydropentalenes enroute to terpenoids Tetrahedron. 43: 5995-6000. DOI: 10.1016/S0040-4020(01)87805-4 |
0.417 |
|
| 1987 |
Ghosh S, Raychaudhuri SR, Salomon RG. Synthesis of cyclobutanated butyrolactones via copper(I)-catalyzed intermolecular photocycloadditions of homoallyl vinyl or diallyl ethers Journal of Organic Chemistry. 52: 83-90. |
0.591 |
|
| 1986 |
Bhide RS, Levison BS, Sharma RB, Ghosh S, Salomon RG. Di-tert-butylmethylsilyl (DTBMS) trifluoromethanesulfonate. Preparation and synthetic applications of DTBMS esters and enol ethers Tetrahedron Letters. 27: 671-674. DOI: 10.1016/S0040-4039(00)84069-1 |
0.773 |
|
| 1985 |
Ghosh S, Saha S. Photo-Induced diels-alder reaction. A novel route to trans fused benzobicyclo-[5.3.O]decanes and [5.4.O]undecanes Tetrahedron Letters. 26: 5325-5326. DOI: 10.1016/S0040-4039(00)95029-9 |
0.329 |
|
| 1985 |
Ghosh S, Saha S. Benzocycloenones as dienophiles. Stereocontrolled synthesis of benzohydropentalene and benzohydroazulene Tetrahedron. 41: 349-355. DOI: 10.1016/S0040-4020(01)96426-9 |
0.444 |
|
| 1985 |
Kanjilal PR, Sarkar M, Patra SK, Ghosh S, Ghatak UR. Synthetic studies toward complex diterpenoids. 16. A novel synthetic route to the carbocyclic skeleta of stemodin and stemarin by acid-catalyzed intramolecular C-alkylation and rearrangement reactions The Journal of Organic Chemistry. 50: 857-863. DOI: 10.1002/Chin.198533323 |
0.611 |
|
| 1984 |
Salomon RG, Ghosh S, Raychaudhuri SR, Miranti TS. Synthesis of multicyclic pyrrolidines via copper(I) catalyzed photobicyclization of ethyl N,N-diallyl carbamates Tetrahedron Letters. 25: 3167-3170. DOI: 10.1016/S0040-4039(01)90999-2 |
0.76 |
|
| 1984 |
SALOMON RG, GHOSH S, RAYCHAUDHURI SR, MIRANTI TS. ChemInform Abstract: COPPER(I) CATALYSIS OF OLEFIN PHOTOREACTIONS. 12. SYNTHESIS OF MULTICYCLIC PYRROLIDINES VIA COPPER(I)-CATALYZED PHOTOBICYCLIZATION OF ETHYL N,N-DIALLYLCARBAMATES Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198447185 |
0.78 |
|
| 1982 |
Salomon RG, Ghosh S, Zagorski MG, Reitz M. Copper (I) catalysis of olefin photoreactions. 10. Synthesis of multicyclic carbon networks by photobicyclization Journal of Organic Chemistry. 47: 829-836. DOI: 10.1021/Jo00344A016 |
0.713 |
|
| 1982 |
Ghatak U, Sanyal B, Ghosh S, Sarkar M, Raju M, Wenkert E. Additions and Corrections - A Formylation-Cyclization Method of Synthesis of Cycloalkenones from Unsaturated Ketones The Journal of Organic Chemistry. 47: 5426-5426. DOI: 10.1021/Jo00148A603 |
0.642 |
|
| 1982 |
Ghosh S, Pardo SN, Salomon RG. Ester enolates from .alpha.-acetoxy esters. Synthesis of arylmalonic and .alpha.-arylalkanoic esters from aryl nucleophiles and .alpha.-keto esters The Journal of Organic Chemistry. 47: 4692-4702. DOI: 10.1021/Jo00145A017 |
0.562 |
|
| 1982 |
Salomon RG, Coughlin DJ, Ghosh S, Zagorski MG. Copper(I) catalysis of olefin photoreactions. 9. Photobicyclization of .alpha.-, .beta.-, and .gamma.-alkenylallyl alcohols Journal of the American Chemical Society. 104: 998-1007. DOI: 10.1021/Ja00368A014 |
0.674 |
|
| 1982 |
Ghosh S, Pardo SN, Salomon RG. Ester enolates from α-acetoxy esters. Synthesis of aryl malonic and α-aryl alkanoic esters from aryl nucleophiles and α-keto esters Journal of Organic Chemistry. 47: 4692-4702. DOI: 10.1002/Chin.198313187 |
0.55 |
|
| 1982 |
Raychaudhuri SR, Ghosh S, Salomon RG. Copper(I) catalysis of olefin photoreactions. 11. Synthesis of multicyclic furans and butyrolactones via photobicyclization of homoallyl vinyl and diallyl ethers Journal of the American Chemical Society. 104: 6841-6842. DOI: 10.1002/Chin.198310206 |
0.801 |
|
| 1982 |
SALOMON RG, COUGHLIN DJ, GHOSH S, ZAGORSKI MG. ChemInform Abstract: COPPER(I) CATALYSIS OF OLEFIN PHOTOREACTIONS. 9. PHOTOBICYCLIZATION OF α-, β-, AND Γ-ALKENYLALLYL ALCOHOLS Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198223129 |
0.693 |
|
| 1981 |
Ghatak UR, Sanyal B, Satyanarayana GOSV, Ghosh S. Acid-catalysed intramolecular C-alkylation in βγ-unsaturated diazomethyl ketones. A new synthetic route to angularly fused cyclobutanones, bridged cyclopentanones, and γ-lactones Journal of the Chemical Society-Perkin Transactions 1. 12: 1203-1212. DOI: 10.1039/P19810001203 |
0.545 |
|
| 1981 |
Ghosh S, Ghatak UR. Novel synthetic route to angularly functionalized hydrofluorene derivatives by a regio- and stereospecific metalation-carbonation reaction The Journal of Organic Chemistry. 46: 1486-1490. DOI: 10.1021/Jo00320A051 |
0.568 |
|
| 1981 |
Pardo SN, Ghosh S, Salomon RG. Generation of ester enolates by reductive a-deacetoxylation Tetrahedron Letters. 22: 1885-1888. DOI: 10.1016/S0040-4039(01)90468-X |
0.576 |
|
| 1980 |
Ghatak UR, Ghosh S, Sanyal B. Synthetic studies towards complex diterpenoids. Part 13. Stereo-specific synthesis of intermediates to the diterpene alkaloids and the C20-gibberellins by a novel rearrangement of angularly fused cyclo-butanones Journal of the Chemical Society-Perkin Transactions 1. 12: 2881-2886. DOI: 10.1039/P19800002881 |
0.557 |
|
| 1980 |
Ghosh S, Dasgupta R, Chakravarty J, Ghatak UR. Synthetic studies towards complex diterpenoids. Part 11. Stereochemically defined synthesis of the racemates of 1,2,3,4,4a,9a-hexahydro-7-methoxy-1-methylfluorene-1-carboxylic acid Journal of the Chemical Society-Perkin Transactions 1. 11: 804-808. DOI: 10.1039/P19800000804 |
0.558 |
|
| 1980 |
Ghatak UR, Sanyal B, Ghosh S, Sarkar M, Raju MS, Wenkert E. A formylation-cyclization method of synthesis of cycloalkenones from unsaturated ketones The Journal of Organic Chemistry. 45: 1081-1085. DOI: 10.1021/jo01294a031 |
0.609 |
|
| 1980 |
Ghatak UR, Sanyal B, Ghosh S, Sarkar M, Raju MS, Wenkert E. A formylation-cyclization method of synthesis of cycloalkenones from unsaturated ketones Journal of Organic Chemistry. 45: 1081-1085. DOI: 10.1021/Jo01294A031 |
0.646 |
|
| 1976 |
Ghatak UR, Sanyal B, Ghosh S. A novel rearrangement of angularly fused cyclobutanone. Stereospecific syntheses of intermediates to the diterpene alkaloids and the C20 gibberellins Journal of the American Chemical Society. 98: 3721-3722. DOI: 10.1021/Ja00428A063 |
0.585 |
|
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