| Year |
Citation |
Score |
| 2012 |
Srikrishna A, Mahesh K. Enantiospecific first total synthesis of ent-Allothapsenol Synlett. 23: 1021-1024. DOI: 10.1055/S-0031-1290527 |
0.546 |
|
| 2012 |
Srikrishna A, Nagaraju G. An Enantiospecific Formal Total Synthesis of the 5-8-5 Tricyclic Diterpene ent-Fusicoauritone Synlett. 2012: 123-127. DOI: 10.1055/S-0031-1290095 |
0.595 |
|
| 2012 |
Srikrishna A, Nagaraju G. The substrate dependent competitive formation of cyclobutanones and cyclopentanones in an intramolecular rhodium carbenoid CH insertion reaction: enantiospecific total synthesis of silphiperfol-6-ene Tetrahedron-Asymmetry. 23: 170-175. DOI: 10.1016/J.Tetasy.2012.01.016 |
0.466 |
|
| 2012 |
Srikrishna A, Gowri V. Enantiospecific total synthesis of 15-hydroxy-5-(methoxymethoxy)crinipellin-9-one Tetrahedron. 68: 3046-3055. DOI: 10.1016/J.Tet.2012.02.018 |
0.567 |
|
| 2012 |
Srikrishna A, Nagaraju G, Sheth VM. Enantiospecific first total synthesis of (6S,7R)-silphiperfolan-6-ol Tetrahedron. 68: 2650-2656. DOI: 10.1016/J.Tet.2012.01.063 |
0.51 |
|
| 2011 |
Srikrishna A, Gowri V. An Enantiospecific Approach to Tetraquinane Diterpenes Crinipellins: Synthesis of Norcrinipellins Synlett. 2011: 2652-2656. DOI: 10.1055/S-0031-1289533 |
0.566 |
|
| 2011 |
Srikrishna A, Sheth VM, Nagaraju G. Rhodium Carbenoid MediatedC-H Activation of a Tertiary Methyl Group: An EnantiospecificApproach to the Angular Triquinanes Norsilphiperfolane and Norcameroonanes Synlett. 2011: 2343-2346. DOI: 10.1055/S-0030-1260308 |
0.467 |
|
| 2011 |
Srikrishna A, Gowri V. Enantiospecific synthesis of angular triquinanes Tetrahedron-Asymmetry. 22: 1553-1559. DOI: 10.1016/J.Tetasy.2011.08.016 |
0.596 |
|
| 2011 |
Srikrishna A, Neetu G. Enantiospecific synthesis of the ABC and ABD ring systems of the marine diterpenes aberraranes Tetrahedron. 67: 7581-7585. DOI: 10.1016/J.Tet.2011.07.054 |
0.485 |
|
| 2010 |
Srikrishna A, Nagaraju G, Ravi G. An Enantiospecific Approach to the 5-8-5 Tricyclic System of Basmanes Synlett. 2010: 3015-3018. DOI: 10.1055/S-0030-1259073 |
0.569 |
|
| 2010 |
Srikrishna A, Pardeshi VH, Mahesh K. Enantiospecific synthesis and confirmation of the relative and absolute stereostructure of 11-hydroxyguaiadienes Tetrahedron Asymmetry. 21: 2830-2833. DOI: 10.1016/J.Tetasy.2010.11.018 |
0.506 |
|
| 2010 |
Srikrishna A, Pardeshi VH, Mahesh K. Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone Tetrahedron Asymmetry. 21: 2512-2516. DOI: 10.1016/J.Tetasy.2010.09.008 |
0.506 |
|
| 2010 |
Srikrishna A, Neetu G. Chiral synthons from campholenaldehyde: enantiospecific synthesis of diquinane and linear triquinanes Tetrahedron-Asymmetry. 21: 2067-2071. DOI: 10.1016/J.Tetasy.2010.06.020 |
0.542 |
|
| 2010 |
Srikrishna A, Pardeshi VH, Satyanarayana G. Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction Tetrahedron-Asymmetry. 21: 746-750. DOI: 10.1016/J.Tetasy.2010.04.003 |
0.585 |
|
| 2010 |
Srikrishna A, Babu RR, Beeraiah B. Enantiospecific synthesis of the tricyclic core structure of lippifolianes Tetrahedron-Asymmetry. 21: 719-724. DOI: 10.1016/J.Tetasy.2010.04.001 |
0.538 |
|
| 2010 |
Srikrishna A, Gowri V, Neetu G. Enantioselective syntheses of diquinane and (cis, anti, cis)-linear triquinanes Tetrahedron-Asymmetry. 21: 202-207. DOI: 10.1016/J.Tetasy.2010.01.014 |
0.419 |
|
| 2010 |
Srikrishna A, Pardeshi VH. Enantiospecific total synthesis of aciphyllene Tetrahedron. 66: 8160-8168. DOI: 10.1016/J.Tet.2010.08.045 |
0.578 |
|
| 2010 |
Srikrishna A, Sridharan M, Prasad KR. Reaction of dialkyl 2-butynoate with aniline and formaldehyde: revision of the structure of the product Tetrahedron. 66: 3651-3654. DOI: 10.1016/J.Tet.2010.03.084 |
0.66 |
|
| 2010 |
Srikrishna A, Babu RR, Beeraiah B. Enantiospecific synthesis of ABC-ring system of A-nor and abeo 4(3→2) tetra and pentacyclic triterpenes Tetrahedron. 66: 852-861. DOI: 10.1016/J.Tet.2009.11.114 |
0.543 |
|
| 2010 |
SRIKRISHNA A, REDDY TJ. ChemInform Abstract: Chiral Synthons from Carvone. Part 34. Enantiospecific Synthesis of (+)-(1S,2R,6S)-1,2-Dimethylbicyclo[4.3.0]nonan-8-one and (-)-7-Epibakkenolide-A. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199901187 |
0.382 |
|
| 2010 |
SRIKRISHNA A, REDDY TJ. ChemInform Abstract: Chiral Synthons from Carvone. Part 21. Bridged Systems via Radical Cyclization Reactions. Stereospecific Synthesis of Chiral Tricyclo(6.2. 1.01,5)undecanes. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199701259 |
0.474 |
|
| 2010 |
SRIKRISHNA A, REDDY TJ. ChemInform Abstract: Enantioselective Formal Total Synthesis of (-)-Homogynolide-A. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199552249 |
0.5 |
|
| 2010 |
SRIKRISHNA A, SHARMA GVR. ChemInform Abstract: Chiral Synthons from Carvone. Part 10. Synthesis of (+)-(1S,3S,4S,7S, 8R)-5,7-Dimethyl-10-oxatetracyclo-(5.3.0.03,5,04,8)decan-9-one. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199444196 |
0.327 |
|
| 2010 |
SRIKRISHNA A, SHARMA GVR. ChemInform Abstract: 1,3-Dicarboxybenzannulation of Acyl Systems via a One-Pot Michael- Michael-Intramolecular Aldol-Dehydration Reaction Sequence. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199347079 |
0.383 |
|
| 2010 |
SRIKRISHNA A, NAGARAJU S. ChemInform Abstract: Synthesis of (.+-.)-β-Cuparenone via 3-Oxa-β-cuparenone. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199204250 |
0.295 |
|
| 2009 |
Srikrishna A, Beeraiah B, Gowri V. Enantiospecific approach to the tricyclic core structure of tricycloillicinone, ialibinones, and takaneones via ring-closing metathesis reaction Tetrahedron. 65: 2649-2654. DOI: 10.1016/J.Tet.2009.01.096 |
0.542 |
|
| 2008 |
Srikrishna A, Ravi G, Krishnan HS. The First Total Syntheses of the Sesquiterpenes (±)-1,10;7,10-Bisepoxy-1,10-seco-calamanene and (±)-6,7;7,10-Bisepoxy-6,7-seco-calamanene Synlett. 2008: 1199-1201. DOI: 10.1055/S-2008-1072733 |
0.475 |
|
| 2008 |
Srikrishna A, Ravikumar P, Krishnan H. The First Total Synthesis of (±)-Herbertenones A and B Synthesis. 2008: 1527-1534. DOI: 10.1055/S-2008-1072560 |
0.816 |
|
| 2008 |
Srikrishna A, Pardeshi VH, Satyanarayana G. Enantiospecific approaches to bicyclic vibsanes: a ring-closing metathesis reaction-based strategy to functionalized bicyclo[4.3.1]decanes Tetrahedron-Asymmetry. 19: 1984-1991. DOI: 10.1016/J.Tetasy.2008.08.012 |
0.571 |
|
| 2008 |
Srikrishna A, Pardeshi VH, Thriveni P. A rapid and efficient enantiospecific synthesis of the functionalized ABC-ring system of tetranortriterpene dumsins and their analogues Tetrahedron-Asymmetry. 19: 1392-1396. DOI: 10.1016/J.Tetasy.2008.05.015 |
0.599 |
|
| 2008 |
Srikrishna A, Beeraiah B. Enantioselective syntheses of cis, syn, cis- and cis, anti, cis-linear triquinanes Tetrahedron-Asymmetry. 19: 884-890. DOI: 10.1016/J.Tetasy.2008.03.007 |
0.377 |
|
| 2008 |
Srikrishna A, Beeraiah B, Babu RR. Enantioselective total synthesis and assignment of the absolute configuration of (+)-laurokamurene B Tetrahedron-Asymmetry. 19: 624-627. DOI: 10.1016/J.Tetasy.2008.02.010 |
0.51 |
|
| 2008 |
Srikrishna A, Babu RR. Total synthesis of (±)-β-chamigrene and (±)-laurencenone C via Ireland ester Claisen rearrangement and an intramolecular type II carbonyl ene reaction sequence Tetrahedron. 64: 10501-10506. DOI: 10.1016/J.Tet.2008.08.095 |
0.537 |
|
| 2008 |
Srikrishna A, Ravi G. A stereoselective total synthesis of (−)-seychellene Tetrahedron. 64: 2565-2571. DOI: 10.1016/J.Tet.2008.01.035 |
0.556 |
|
| 2007 |
Srikrishna A, Ratna Kumar S, Ravikumar PC. Synthesis of (±)‐12‐Methoxyherbertenediol Dimethyl Ether Synthetic Communications. 37: 4123-4140. DOI: 10.1080/00397910701574577 |
0.817 |
|
| 2007 |
Srikrishna A, Beeraiah B. Synthesis of (±)‐ar‐Macrocarpene Synthetic Communications. 37: 2855-2860. DOI: 10.1080/00397910701470727 |
0.538 |
|
| 2007 |
Srikrishna A, Satyanarayana G, Prasad KR. RCM-based approach to (±)-cuparene Synthetic Communications. 37: 1511-1516. DOI: 10.1080/00397910701229214 |
0.701 |
|
| 2007 |
Srikrishna A, Satyanarayana G, Desai UV. Efficient Approach to 4-Benzyl-5,5-dimethyldihydrofuranones: Total Synthesis of ($\pm$_bold;)-Solafuranone Synthetic Communications. 37: 965-976. DOI: 10.1080/00397910601163919 |
0.501 |
|
| 2007 |
Srikrishna A, Babu R, Ravikumar P. A Regioselective Total Synthesis of the Fungal Sesquiterpene (±)-Lagopodin A Synlett. 2007: 0655-0657. DOI: 10.1055/S-2007-967971 |
0.843 |
|
| 2007 |
Srikrishna A, Ravikumar P. The First Total Synthesis of (±)-γ-Herbertenol, a Herbertene Isolated from a Non-Herbertus Source Synthesis. 2007: 65-74. DOI: 10.1055/S-2006-950355 |
0.809 |
|
| 2007 |
Srikrishna A, Lakshmi BV, Sudhakar AVS. Pyridinium chlorochromate mediated oxidative cyclisation of sterically crowded γ,δ-unsaturated alcohols Tetrahedron Letters. 48: 7610-7613. DOI: 10.1016/J.Tetlet.2007.08.112 |
0.385 |
|
| 2007 |
Srikrishna A, Babu RR. Total syntheses of (±)-α-acorenol, β-acorenol, α-epi-acorenol and β-epi-acorenol via an Ireland ester Claisen rearrangement and RCM reaction sequence Tetrahedron Letters. 48: 6916-6919. DOI: 10.1016/J.Tetlet.2007.07.163 |
0.453 |
|
| 2007 |
Srikrishna A, Pardeshi VH, Satyanarayana G. A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes Tetrahedron Letters. 48: 4087-4090. DOI: 10.1016/J.Tetlet.2007.04.005 |
0.563 |
|
| 2007 |
Srikrishna A, Beeraiah B. Synthetic approaches to komarovispiranes. Enantiospecific synthesis of bicyclo[3.3.0]octanespiro[3.1′]cyclohexanes Tetrahedron Letters. 48: 2291-2294. DOI: 10.1016/J.Tetlet.2007.01.160 |
0.54 |
|
| 2007 |
Srikrishna A, Ravi G, Satyanarayana G. The first enantiospecific total synthesis of (+)-seychellene Tetrahedron Letters. 48: 73-76. DOI: 10.1016/J.Tetlet.2006.11.011 |
0.563 |
|
| 2007 |
Srikrishna A, Beeraiah B. An enantiospecific synthesis of a komarovispirane Tetrahedron-Asymmetry. 18: 2587-2597. DOI: 10.1016/J.Tetasy.2007.10.030 |
0.557 |
|
| 2007 |
Srikrishna A, Gowri V. Synthetic approaches to neorogiolanes: enantiospecific synthesis of 12-methoxyneorogiola-1,3,5,7(17),8-pentaene Tetrahedron-Asymmetry. 18: 1663-1666. DOI: 10.1016/J.Tetasy.2007.07.007 |
0.535 |
|
| 2007 |
Srikrishna A, Khan IA, Babu RR, Sajjanshetty A. The first total synthesis of (±)-laurokamurene B Tetrahedron. 63: 12616-12620. DOI: 10.1016/J.Tet.2007.10.021 |
0.56 |
|
| 2006 |
Srikrishna A, Lakshmi BV, Mathews M. Construction of spiro[5.5]undecanes containing a quaternary carbon atom adjacent to a spirocentre via an Ireland ester Claisen rearrangement and RCM reaction sequence. Total syntheses of (±)-α-chamigrene, (±)-β-chamigrene and (±)-laurencenone C Tetrahedron Letters. 47: 2103-2106. DOI: 10.1016/J.Tetlet.2006.01.131 |
0.509 |
|
| 2006 |
Srikrishna A, Vasantha Lakshmi B, Ravikumar P. The first total synthesis of (±)-lagopodin A Tetrahedron Letters. 47: 1277-1281. DOI: 10.1016/J.Tetlet.2005.12.071 |
0.831 |
|
| 2006 |
Srikrishna A, Ramasastry S. Enantiospecific first total synthesis of (+)-2β-hydroxysolanascone, the aglycone of the phytoalexin isolated from flue-cured tobacco leaves Tetrahedron Letters. 47: 335-339. DOI: 10.1016/J.Tetlet.2005.11.014 |
0.764 |
|
| 2006 |
Srikrishna A, Satyanarayana G. A biogenetically patterned enantiospecific synthesis of allopupukeanones Tetrahedron Letters. 47: 367-370. DOI: 10.1016/J.Tetlet.2005.11.009 |
0.487 |
|
| 2006 |
Srikrishna A, Satyanarayana G, Kumar PR. Enantiospecific synthesis of tricyclo[5.2.1.04,8]decanes via acid catalysed rearrangement of isotwistanes Tetrahedron Letters. 47: 363-366. DOI: 10.1016/J.Tetlet.2005.11.008 |
0.464 |
|
| 2006 |
Srikrishna A, Beeraiah B, Satyanarayana G. Chiral synthons from α-pinene: enantioselective syntheses of bicyclo[3.3.0] and [3.2.1]octanones Tetrahedron-Asymmetry. 17: 1544-1548. DOI: 10.1016/J.Tetasy.2006.05.028 |
0.541 |
|
| 2006 |
Srikrishna A, Ravikumar P. Structure revision of HM-3, an aromatic sesquiterpene isolated from the phytopathogenic fungus Helicobasidium mompa. First total syntheses of HM-3 and HM-4 Tetrahedron. 62: 9393-9402. DOI: 10.1016/J.Tet.2006.07.062 |
0.817 |
|
| 2006 |
Srikrishna A, Satyanarayana G. Total synthesis of (±)-herbertenediol Tetrahedron. 62: 2892-2900. DOI: 10.1016/J.Tet.2006.01.021 |
0.571 |
|
| 2005 |
Sitalakshmi S, Srikrishna A, Devi S, Damodar P, Alexander B. The diagnostic utility of bone marrow trephine biopsies. Indian Journal of Pathology & Microbiology. 48: 173-6. PMID 16758657 |
0.182 |
|
| 2005 |
Sitalakshmi S, Srikrishna A, Damodar P. Plasmodium malariae malaria--a case report. Journal of the Indian Medical Association. 103: 547, 550. PMID 16498762 |
0.177 |
|
| 2005 |
Sitalakshmi S, Srikrishna A, Shanthala DA, Damodar P. Does ISI of thromboplastin affect the INR value? The Journal of the Association of Physicians of India. 53: 493-4. PMID 16124366 |
0.16 |
|
| 2005 |
Srikrishna A, Rao MS. Synthesis of herbertenediol and mastigophorenes A-D Arkivoc. 2005. DOI: 10.3998/Ark.5550190.0006.B16 |
0.428 |
|
| 2005 |
Srikrishna A, Satyanarayana G, Prasad MR. Synthetic approaches to sporochnols A-C Synthetic Communications. 35: 1687-1698. DOI: 10.1081/Scc-200061679 |
0.428 |
|
| 2005 |
Srikrishna A, Lakshmi BV. Formal Total Synthesis of (±)-Herbertene-1,13-diol and (±)-α-Herbertenol via Ireland Ester Claisen Rearrangement and RCM Reaction Sequence Synlett. 2005: 1173-1175. DOI: 10.1055/S-2005-865223 |
0.573 |
|
| 2005 |
Srikrishna A, Ramasastry S. Enantiospecific total synthesis of phytoalexins, (+)-solanascone, (+)-dehydrosolanascone, and (+)-anhydro-β-rotunol Tetrahedron Letters. 46: 7373-7376. DOI: 10.1016/J.Tetlet.2005.08.124 |
0.791 |
|
| 2005 |
Srikrishna A, Lakshmi BV. The first total synthesis of a bioactive metabolite, a spirobenzofuran isolated from the fungi Acremonium sp. HKI 0230 Tetrahedron Letters. 46: 7029-7031. DOI: 10.1016/J.Tetlet.2005.08.049 |
0.503 |
|
| 2005 |
Srikrishna A, Ravikumar P. Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2 Tetrahedron Letters. 46: 6105-6109. DOI: 10.1016/J.Tetlet.2005.06.156 |
0.817 |
|
| 2005 |
Srikrishna A, Lakshmi BV. Construction of vicinal quaternary carbon atoms by Ireland ester Claisen rearrangement: total synthesis of (±)-herbertenolide, (±)-herberteneacetal, (±)-herbertene-1,14-diol and (±)-herbertene-1,15-diol Tetrahedron Letters. 46: 4879-4881. DOI: 10.1016/J.Tetlet.2005.05.065 |
0.502 |
|
| 2005 |
Srikrishna A, Dethe DH. An efficient construction of a C3-symmetric macrocycle by head to tail cyclotrimerization of an unsymmetrical diene via a sequence of highly regio- and stereoselective metathesis reactions Tetrahedron Letters. 46: 3381-3383. DOI: 10.1016/J.Tetlet.2005.03.088 |
0.787 |
|
| 2005 |
Srikrishna A, Satyanarayana G. An enantiospecific total synthesis of (-)-patchouli alcohol Tetrahedron-Asymmetry. 16: 3992-3997. DOI: 10.1016/J.Tetasy.2005.11.012 |
0.52 |
|
| 2005 |
Srikrishna A, Ramasastry SS. A novel boron trifluoride etherate mediated deep-seated rearrangement of an α,β-epoxyketone Tetrahedron: Asymmetry. 16: 2973-2979. DOI: 10.1016/J.Tetasy.2005.07.030 |
0.805 |
|
| 2005 |
Srikrishna A, Dinesh C. Competitive formation of spiro[5.5]undecane in preference to bicyclo[4.3.1]decane via type II carbonyl ene reaction Tetrahedron-Asymmetry. 16: 2393-2395. DOI: 10.1016/J.Tetasy.2005.06.011 |
0.407 |
|
| 2005 |
Srikrishna A, Dinesh C. Stereo- and regioselective construction of vicinal stereogenic quaternary carbon atoms: enantiospecific approach to cyperanes Tetrahedron-Asymmetry. 16: 2203-2207. DOI: 10.1016/J.Tetasy.2005.05.021 |
0.449 |
|
| 2005 |
Srikrishna A, Nagamani SA, Jagadeesh SG. The first enantioselective synthesis of (−)-microbiotol and (+)-β-microbiotene Tetrahedron-Asymmetry. 16: 1569-1571. DOI: 10.1016/J.Tetasy.2005.03.009 |
0.551 |
|
| 2005 |
Srikrishna A, Satyanarayana G. A formal total synthesis of (′)-9-isocyanoneopupukeanane Tetrahedron. 61: 8855-8859. DOI: 10.1016/J.Tet.2005.07.016 |
0.588 |
|
| 2004 |
Srikrishna A, Sitalakshmi S, Devi S, Damodar P, Varghese J, Suresh J, Mathew T. Antiphospholipid antibodies--our experience. Indian Journal of Pathology & Microbiology. 47: 174-7. PMID 16295461 |
0.168 |
|
| 2004 |
Srikrishna A, Satyanarayana G. Enantioselective total synthesis of valeriananoids A-C. Organic Letters. 6: 2337-9. PMID 15228273 DOI: 10.1021/Ol049341Y |
0.569 |
|
| 2004 |
Srikrishna A, Dethe DH. Synthetic approaches to guanacastepenes. Enantiospecific syntheses of BC and AB ring systems of guanacastepenes and rameswaralide. Organic Letters. 6: 165-8. PMID 14723519 DOI: 10.1021/Ol036057I |
0.811 |
|
| 2004 |
Srikrishna A, Satyanarayana G. Total synthesis of (′)-infuscol A and (′)-cuprenenol Synthetic Communications. 34: 3847-3864. DOI: 10.1081/Scc-200034755 |
0.543 |
|
| 2004 |
Srikrishna A, Rao MS. The First Total Synthesis of the Antimicrobial Sesquiterpenes (±)-Enokipodins A and B Synlett. 2004: 374-376. DOI: 10.1055/S-2003-45003 |
0.588 |
|
| 2004 |
Srikrishna A, Kumar PR. Enantiospecific first total synthesis of (+)-trans-α-himachalene Tetrahedron Letters. 45: 6867-6870. DOI: 10.1016/J.Tetlet.2004.07.103 |
0.513 |
|
| 2004 |
Srikrishna A, Dethe DH, Ravi Kumar P. Enantiospecific construction of the BC-ring system of taxanes Tetrahedron Letters. 45: 2939-2942. DOI: 10.1016/J.Tetlet.2004.02.075 |
0.807 |
|
| 2004 |
Srikrishna A, Ravi Kumar P, Ramasastry S. Corrigendum to ‘Carbanion cyclisation of esters. Part 2: Enantiospecific construction of the tricyclic framework of the marine sesquiterpenes, spirodysins’ Tetrahedron Letters. 45: 2261. DOI: 10.1016/J.Tetlet.2004.01.052 |
0.784 |
|
| 2004 |
Srikrishna A, Ravi Kumar P, Ramasastry S. Carbanion cyclisation of esters. Part 2: 1See Reference 1. 1 Enantiospecific construction of the tricyclic framework of the marine sesquiterpenes, spirodysins Tetrahedron Letters. 45: 383-386. DOI: 10.1016/J.Tetlet.2003.10.165 |
0.791 |
|
| 2004 |
Srikrishna A, Ramasastry S. Lithium–liquid ammonia mediated carbocyclisation of δ,ε-unsaturated esters: annulation of cyclopentanones Tetrahedron Letters. 45: 379-382. DOI: 10.1016/J.Tetlet.2003.10.164 |
0.795 |
|
| 2004 |
Srikrishna A, Dethe DH. An Efficient Ring-Closing Metathesis Reaction of Geminally Disubstituted Olefins Using First Generation Grubbs′ Catalyst: Enantiospecific Synthesis of Pacifigorgianes. Cheminform. 35. DOI: 10.1016/J.Tetlet.2003.08.076 |
0.807 |
|
| 2004 |
Srikrishna A, Babu NC, Rao MS. A stereoselective total synthesis of (+)-α-herbertenol Tetrahedron. 60: 2125-2130. DOI: 10.1016/J.Tet.2003.12.055 |
0.55 |
|
| 2003 |
Sitalakshmi S, Srikrishna A, Devi S, Damodar P, Mathew T, Varghese J. Changing trends in malaria--a decade's experience at a referral hospital. Indian Journal of Pathology & Microbiology. 46: 399-401. PMID 15025283 |
0.184 |
|
| 2003 |
Sitalakshmi S, Srikrishna A, Damodar P. Haematological changes in HIV infection. Indian Journal of Pathology & Microbiology. 46: 180-3. PMID 15022904 |
0.172 |
|
| 2003 |
Srikrishna A, Dethe DH. Enantiospecific first total synthesis and assignment of absolute configuration of the sesquiterpene (-)-cucumin H. Organic Letters. 5: 2295-8. PMID 12816432 DOI: 10.1021/Ol034635P |
0.805 |
|
| 2003 |
Srikrishna A, Shaktikumar L, Satyanarayana G. The first synthesis of (±)-secocuparenal, a sesquiterpene isolated from the liverwort Jungermannia infusca Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.909 |
0.474 |
|
| 2003 |
Srikrishna A, Kumar PP, Reddy TJ. Enantiospecific synthesis of functionalised bicyclo[3.3.1]nonanes from 10-bromocarvones via tandem intermolecular alkylation-intramolecular Michael addition sequence Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.307 |
0.559 |
|
| 2003 |
Singh V, Srikrishna A. A Tribute to Prof. Sukh Dev Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.301 |
0.285 |
|
| 2003 |
Srikrishna A, Jagadeeshwar Reddy T, Palani N, Balasubramanian KK. A Stereospecific Approach tocis-anti-cisTriquinanes Synthetic Communications. 33: 1537-1544. DOI: 10.1081/Scc-120018772 |
0.698 |
|
| 2003 |
Srikrishna A, Viswajanani R, Sattigeri JA. A radical cyclisation based cyclopentenone annulation of allyl alcohols Tetrahedron-Asymmetry. 14: 2975-2983. DOI: 10.1016/S0957-4166(03)00535-4 |
0.52 |
|
| 2003 |
Srikrishna A, Satyanarayana G. Total synthesis of (±)-1,13-herbertenediol, (±)-α-herbertenol and (±)-β-herbertenol Tetrahedron Letters. 44: 1027-1030. DOI: 10.1016/S0040-4039(02)02734-X |
0.514 |
|
| 2003 |
Srikrishna A, Anebouselvy K. Enantiospecific first total synthesis of (+)-cis,anti,cis-3-hydroxy-1,8,12,12-tetramethyl-4-oxatricyclo[6.4.0.02,6]dodecan-9-yl senecioate, the optical antipode of a natural thapsane isolated from Thapsia villosa Tetrahedron Letters. 44: 1031-1034. DOI: 10.1016/S0040-4039(02)02733-8 |
0.467 |
|
| 2002 |
Srikrishna A, Sitalakshmi S, Shantala Devi AM, Damodar P, D'Souza GA. Disseminated histoplasmosis in an AIDS patient diagnosed on bone marrow. Indian Journal of Pathology & Microbiology. 45: 333-4. PMID 12785178 |
0.178 |
|
| 2002 |
Srikrishna A, Gharpure SJ. Enantiospecific synthesis of (-)-4-thiocyanatoneopupukeanane Arkivoc. 2002. DOI: 10.3998/Ark.5550190.0003.707 |
0.806 |
|
| 2002 |
Srikrishna A, Kumar PR, Padmavathi V. An Enantiospecific Approach to 8,9-seco-C-Aromatic Taxanes Synlett. 2002: 1907-1909. DOI: 10.1055/S-2002-34902 |
0.441 |
|
| 2002 |
Srikrishna A, Rao MS. A ring closing metathesis-based approach to(±)-herbertene,(±)-α-herbertenol,(±)-β-herbertenol and (±)-herbertenediol Synlett. 2002: 340-342. DOI: 10.1055/S-2002-19750 |
0.487 |
|
| 2002 |
Srikrishna A, Anebouselvy K. The first enantiospecific synthesis of (+)-10,11-epoxythapsan-10-ol: revision of the absolute stereochemistry of thapsanes Tetrahedron Letters. 43: 5261-5264. DOI: 10.1016/S0040-4039(02)01051-1 |
0.478 |
|
| 2002 |
Srikrishna A, Anebouselvy K. An enantiospecific approach to (+)-thaps-8(11)-en-3-ol Tetrahedron Letters. 43: 2769-2771. DOI: 10.1016/S0040-4039(02)00382-9 |
0.524 |
|
| 2002 |
Srikrishna A, Ramachary DB. Stereospecific construction of three contiguous quaternary carbon atoms. Synthesis of (±)-3-methoxythaps-8-ene Tetrahedron Letters. 43: 2765-2768. DOI: 10.1016/S0040-4039(02)00381-7 |
0.512 |
|
| 2002 |
Srikrishna A, Kumar PR. First enantiospecific synthesis of (−)-9-pupukeanone☆ Tetrahedron Letters. 43: 1109-1111. DOI: 10.1016/S0040-4039(01)02336-X |
0.575 |
|
| 2002 |
Srikrishna A, Rao MS. A simple, ring-closing metathesis reaction based approach to (±)-1,14-herbertenediol and (±)-11-epi-herbertenolide Tetrahedron Letters. 43: 151-154. DOI: 10.1016/S0040-4039(01)02051-2 |
0.58 |
|
| 2001 |
Sitalakshmi S, Tilak P, Srikrishna A, Damodar P, Thomas IM. An unusual case of haemophilia--a case report. Indian Journal of Pathology & Microbiology. 44: 367-8. PMID 12024938 |
0.176 |
|
| 2001 |
Shanthala Devi AM, Srikrishna A, Sitalaksmi S, Damodar P. Clinicohaematological profile of two cases of inhibitors to factor VIII. Indian Journal of Pathology & Microbiology. 44: 365-6. PMID 12024937 |
0.167 |
|
| 2001 |
Srikrishna A, Anebouselvy K. An enantiospecific approach to tricyclic sesquiterpenes mayurone and thujopsenes. The Journal of Organic Chemistry. 66: 7102-6. PMID 11597236 |
0.474 |
|
| 2001 |
Srikrishna A, Gharpure SJ. Enantiospecific total synthesis of (-)-4-thiocyanatoneopupukeanane. The Journal of Organic Chemistry. 66: 4379-85. PMID 11397180 DOI: 10.1021/Jo0102765 |
0.8 |
|
| 2001 |
Srikrishna A, Reddy TJ. Enantiospecific formal total synthesis of homogynolide-A Arkivoc. 2001. DOI: 10.3998/Ark.5550190.0002.802 |
0.571 |
|
| 2001 |
Srikrishna A, Danieldoss S. Radical Cyclisation Based Approach To Lignans. Synthesis Of 4-Arylmethyldihydrofuran-2-Ones Synthetic Communications. 31: 2357-2364. DOI: 10.1081/Scc-100104837 |
0.386 |
|
| 2001 |
Rajalakshmi K, Pattabhi V, Venkatesan CS, Nadamuni G, Srikrishna A. Crystal and molecular structure of synthetic cholesterol compounds vitamin D3-analogues (I) 24(S)-hydroxy coprastan-3-one & (II) 24(R)-hydroxy coprastan-3-one Molecular Crystals and Liquid Crystals. 369: 243-271. DOI: 10.1080/10587250108030021 |
0.402 |
|
| 2001 |
Srikrishna A, Rao MS. Formal total synthesis of (±)-herbertenediol and (±)-mastigophorenes A and B Tetrahedron Letters. 42: 5781-5782. DOI: 10.1016/S0040-4039(01)01109-1 |
0.502 |
|
| 2001 |
Srikrishna A, Babu NC. An enantiospecific formal total synthesis of (−)-aplysin and (−)-debromoaplysin Tetrahedron Letters. 42: 4913-4914. DOI: 10.1016/S0040-4039(01)00842-5 |
0.469 |
|
| 2001 |
Srikrishna A, Kumar PR, Gharpure SJ. An enantiospecific synthesis of (−)-2-pupukeanone via a rhodium carbenoid CH insertion reaction Tetrahedron Letters. 42: 3929-3931. DOI: 10.1016/S0040-4039(01)00585-8 |
0.807 |
|
| 2000 |
Rajalakshmi K, Pattabhi V, Venkatesan CS, Nadamuni G, Srikrishna A. 24(R)-Acetyloxy-1α,2α-epoxycholesta-4,6-dien-3-one hydrate. Erratum Acta Crystallographica Section C-Crystal Structure Communications. 56: 538-538. DOI: 10.1107/S0108270100012993 |
0.408 |
|
| 2000 |
Rajalakshmi K, Pattabhi V, Venkatesan CS, Nadamuni G, Srikrishna A. 24(R)‐Acetyloxy‐1α,2α‐epoxycholesta‐4,6‐dien‐3‐one hydrate Acta Crystallographica Section C-Crystal Structure Communications. 56. DOI: 10.1107/S0108270100007927 |
0.415 |
|
| 2000 |
Srikrishna A, Gharpure SJ. Novel Formation of Chloromethanesulfinates in the Methanesulfonylation Reaction of Hindered Alcohols Synlett. 2000: 1354-1356. DOI: 10.1055/S-2000-7147 |
0.748 |
|
| 2000 |
Srikrishna A, Viswajanani R, Dinesh C. Stereoselective construction of vicinal stereogenic quaternary carbon atoms. Enantiospecific approaches to (+)-valerane Journal of the Chemical Society-Perkin Transactions 1. 4321-4327. DOI: 10.1039/B006757L |
0.534 |
|
| 2000 |
Srikrishna A, Gharpure SJ. Enantiospecific total synthesis of both enantiomers of 2-thiocyanatoneopupukeanane from (R)-carvone Journal of the Chemical Society-Perkin Transactions 1. 3191-3193. DOI: 10.1039/B005943I |
0.806 |
|
| 2000 |
Srikrishna A, Vijaykumar D. An enantiospecific approach to pinguisanes from (R)-carvone. Total synthesis of (+)-pinguisenol Journal of the Chemical Society-Perkin Transactions 1. 2583-2589. DOI: 10.1039/B004770H |
0.557 |
|
| 2000 |
Srikrishna A, Anebouselvy K, Reddy TJ. An enantiospecific approach to thapsanes from R-carvone: synthesis of (−)-thaps-8-en-5-ol Tetrahedron Letters. 41: 6643-6647. DOI: 10.1016/S0040-4039(00)01107-2 |
0.522 |
|
| 2000 |
Srikrishna A, Gharpure SJ, Praveen Kumar P. A simple, enantiospecific approach to both enantiomers of 1α,25-dihydroxyvitamin D3 A-ring precursors from R-carvone Tetrahedron Letters. 41: 3177-3180. DOI: 10.1016/S0040-4039(00)00325-7 |
0.77 |
|
| 2000 |
Srikrishna A, Ramachary DB. The first total synthesis of (±)-grimaldone Tetrahedron Letters. 41: 2231-2233. DOI: 10.1016/S0040-4039(00)00136-2 |
0.478 |
|
| 2000 |
Srikrishna A, Praveen Kumar P. Claisen Rearrangement Based Methodology for the Spiroannulation of a Cyclopentane Ring. Formal Total Synthesis of (±)-Acorone and Isoacorones Tetrahedron. 56: 8189-8195. DOI: 10.1016/S0040-4020(00)00743-2 |
0.595 |
|
| 2000 |
Rajalakshmi K, Pattabhi V, Venkatesan CS, Nadamuni G, Srikrishna A. Crystal structure analysis of synthetic cholesterol compounds-vitamin D3-analogues Crystal Research and Technology. 35: 1383-1394. DOI: 10.1002/1521-4079(200011)35:11/12<1383::Aid-Crat1383>3.0.Co;2-P |
0.405 |
|
| 1999 |
Srikrishna A, Sitalakshmi S, Damodar P. How safe are our safe donors? Indian Journal of Pathology & Microbiology. 42: 411-6. PMID 11127370 |
0.153 |
|
| 1999 |
Yelamaggad CV, Srikrishna A, Rao DSS, Prasad SK. Synthesis and characterization of some new dimesogenic compounds Liquid Crystals. 26: 1547-1554. DOI: 10.1080/026782999203887 |
0.411 |
|
| 1999 |
Srikrishna A, Nagamani AS. A short and efficient regioselective approach to the C-6 to C-19 segment of bifurcaranes and a formal total synthesis of β-microbiotene, microbiotol and cyclocuparanol Journal of the Chemical Society-Perkin Transactions 1. 3393-3394. DOI: 10.1039/A908033C |
0.513 |
|
| 1999 |
Srikrishna A, Yelamaggad CV, Kumar PP. Rearrangement approaches to sesquiterpenes containing multiple contiguous quaternary carbon atoms. Total synthesis of (±)-myltayl-8(12)-ene and (±)-6-epijunicedranol Journal of the Chemical Society-Perkin Transactions 1. 2877-2881. DOI: 10.1039/A906706J |
0.501 |
|
| 1999 |
Srikrishna A, Nagaraju S, Venkateswarlu S, Hiremath US, Reddy TJ, Venugopalan P. A formal total synthesis of (±)-homogynolide-B Journal of the Chemical Society-Perkin Transactions 1. 2069-2076. DOI: 10.1039/A903866C |
0.498 |
|
| 1999 |
Srikrishna A, Vijaykumar D. A formal total synthesis of (±)-α-pinguisene and (±)-pinguisenol Journal of the Chemical Society-Perkin Transactions 1. 1265-1272. DOI: 10.1039/A901519A |
0.534 |
|
| 1999 |
Srikrishna A, Ramachary DB. First total synthesis of (±)-β-microbiotene, (±)-microbiotol and (±)-cyclocuparenol Tetrahedron Letters. 40: 6669-6670. DOI: 10.1016/S0040-4039(99)01342-8 |
0.462 |
|
| 1999 |
Srikrishna A, Ramachary DB. Regioselective synthesis of bicyclo[4.2.1]nonane-2,8-diones via BF3.Et2O mediated intramolecular diazo ketone insertion reaction Tetrahedron Letters. 40: 1605-1606. DOI: 10.1016/S0040-4039(98)02656-2 |
0.447 |
|
| 1999 |
Srikrishna A, Gharpure SJ. Enantiospecific first total synthesis of (−)-4-thiocyanatoneopupukeanane Tetrahedron Letters. 40: 1035-1038. DOI: 10.1016/S0040-4039(98)02522-2 |
0.79 |
|
| 1999 |
Srikrishna A, Dinesh C, Anebouselvy K. Synthesis of chiral bicyclo[4.3.1]decanes via an intramolecular carbonyl ene-reaction Tetrahedron Letters. 40: 1031-1034. DOI: 10.1016/S0040-4039(98)02518-0 |
0.554 |
|
| 1998 |
Srikrishna A, Reddy TJ, Kumar PP. Carvone based approaches to chiral functionalised B-seco-taxanes † Journal of the Chemical Society-Perkin Transactions 1. 3143-3144. DOI: 10.1039/A805862H |
0.508 |
|
| 1998 |
Srikrishna A, Gharpure SJ. An intramolecular rhodium carbenoid C–H insertion approach to chiral isotwistanes. Synthesis of (–)-neopupukean-4,10-dione and (–)-neopupukean-10-one Chemical Communications. 1589-1590. DOI: 10.1039/A804001J |
0.824 |
|
| 1998 |
Srikrishna A, Vijaykumar D. Facile formation of chiral bicyclo[3.3.1]nonenes via regioselective cyclopropane cleavage of 1-methyltricyclo[4.3.0.02,9]nonan-8-ols Tetrahedron Letters. 39: 5833-5834. DOI: 10.1016/S0040-4039(98)01153-8 |
0.544 |
|
| 1998 |
Srikrishna A, Kumar P, Reddy T. Carvone based approaches to chiral functionalised C-ring derivatives of taxanes Tetrahedron Letters. 39: 5815-5818. DOI: 10.1016/S0040-4039(98)01148-4 |
0.535 |
|
| 1998 |
Srikrishna A, Vijaykumar D. Enantiospecific synthesis of (+)-pinguisenol, (+)-pinguisen-10-one and (−)-pinguisen-8,10-dione Tetrahedron Letters. 39: 4901-4904. DOI: 10.1016/S0040-4039(98)00891-0 |
0.516 |
|
| 1998 |
Srikrishna A, Reddy TJ. Enantiospecific synthesis of (+)-(1S,2R,6S)-1,2-dimethylbicyclo[4.3.0]nonan-8-one and (-)-7-epibakkenolide-A Tetrahedron. 54: 11517-11524. DOI: 10.1016/S0040-4020(98)00672-3 |
0.567 |
|
| 1998 |
Srikrishna A, Reddy TJ. Stereoselective total synthesis of (±)-tochuinyl acetate and (±)-dihydrotochuinyl acetates Tetrahedron. 54: 8133-8140. DOI: 10.1016/S0040-4020(98)00436-0 |
0.514 |
|
| 1997 |
Mehta G, Srikrishna A. Synthesis of Polyquinane Natural Products: An Update. Chemical Reviews. 97: 671-720. PMID 11848885 DOI: 10.1021/Cr9403650 |
0.639 |
|
| 1997 |
Srikrishna A, Danieldoss S. Photochemical Rearrangements of Chiral Bicyclo[2.2.2]oct-5-en-2-Ones1 Synthetic Communications. 27: 655-661. DOI: 10.1080/00397919708003339 |
0.486 |
|
| 1997 |
Srikrishna A, Danieldoss S, Sharma GVR. Synthesis of chiral bicyclo[2.2.2]octa-5,7-dien-2-$ones^1$ Synthetic Communications. 27: 601-608. DOI: 10.1080/00397919708003331 |
0.561 |
|
| 1997 |
Srikrishna A, Reddy T, Kumar P. Synthesis of Chiral Bicyclo[3.3.1]nonanes via a Tandem Intermolecular Alkylation-Intramolecular Michael Reaction Sequence Synlett. 1997: 663-664. DOI: 10.1055/S-1997-3247 |
0.566 |
|
| 1997 |
Srikrishna A, Reddy TJ. Enantiospecific total synthesis of (+)-2-pupukeanone Journal of the Chemical Society-Perkin Transactions 1. 3293-3294. DOI: 10.1039/A706321K |
0.592 |
|
| 1997 |
Srikrishna A, Vijaykumar D. Stereocontrolled synthesis of (±)-α-pinguisene and (±)-pinguisenol Journal of the Chemical Society-Perkin Transactions 1. 3295-3296. DOI: 10.1039/A705600A |
0.504 |
|
| 1997 |
Srikrishna A, Sharma GVR. Synthesis of chiral tricyclo[3.2.1.02,7]octanes by anefficient 3-exo-trig radical cyclisationreaction1 Journal of the Chemical Society-Perkin Transactions 1. 177-182. DOI: 10.1039/A601315E |
0.506 |
|
| 1997 |
Srikrishna A, Danieldoss S. Radical Annulation Vs The 3-Exo-Trig Cyclization Via Fine Tuning Of The Substrate Structure Journal of Organic Chemistry. 62: 7863-7865. DOI: 10.1021/Jo9703360 |
0.416 |
|
| 1997 |
Srikrishna A, Viswajanani R, Reddy TJ, Vijaykumar D, Kumar PP. Cyclopropane formation vs the homoallyl homoallyl radical rearrangement in 7-oxygen-substituted norborn-5-en-2-yl radicals Journal of Organic Chemistry. 62: 5232-5234. DOI: 10.1021/Jo970246V |
0.383 |
|
| 1997 |
Srikrishna A, Kumar P. A biogenetically patterned first total synthesis of (±)-6-epijunicedranol (or junicedran-11-ol) Tetrahedron Letters. 38: 2005-2006. DOI: 10.1016/S0040-4039(97)00216-5 |
0.489 |
|
| 1997 |
Srikrishna A, Vijaykumar D, Sharma GVR. A short, vinyl radical cyclisation approach to (±)-2-pupukeanone Tetrahedron Letters. 38: 2003-2004. DOI: 10.1016/S0040-4039(97)00210-4 |
0.431 |
|
| 1997 |
Srikrishna A, Viswajanani R, Yelamaggad CV. Tributyltin chloride-sodium cyanoborohydride mediated tandem radical cyclisation-reductive demethoxylation sequence Tetrahedron. 53: 10479-10488. DOI: 10.1016/S0040-4020(97)00658-3 |
0.416 |
|
| 1997 |
Srikrishna A, Vijaykumar D, Reddy TJ. Enantiospecific synthesis of (+)-dihydroerythrodiene, (+)-dihydrospirojatamol and (+)-dihydroepispirojatamol Tetrahedron. 53: 1439-1446. DOI: 10.1016/S0040-4020(96)01055-1 |
0.552 |
|
| 1997 |
Srikrishna A, Danieldoss S. Variable‐temperature NMR studies of 6‐(o‐tolyl)‐8‐methoxy‐1,8‐dimethylbicyclo[2.2.2]oct‐5‐en‐2‐ones Magnetic Resonance in Chemistry. 35: 829-831. DOI: 10.1002/(Sici)1097-458X(199712)35:12<829::Aid-Omr179>3.0.Co;2-Y |
0.382 |
|
| 1996 |
Srikrishna A, Reddy TJ. Bridged Systems via Radical Cyclization Reactions. Stereospecific Synthesis of Chiral Tricyclo[6.2.1.0(1,5)]undecanes(1). The Journal of Organic Chemistry. 61: 6422-6424. PMID 11667486 DOI: 10.1021/Jo960423C |
0.425 |
|
| 1996 |
Srikrishna A, Reddy TJ, Kumar PP, Vijaykumar D. A methodology for spirocyclopentannulation. Stereoselective total synthesis of (±)-tochuinyl acetate and (±)-dihydrotochuinyl acetate Synlett. 1996: 67-68. DOI: 10.1055/S-1996-5318 |
0.538 |
|
| 1996 |
Srikrishna A, Sharma GVR, Danieldoss S, Hemamalini P. Synthesis of chiral bicyclo[2.2.2]oct-5-en-2-ones via an intramolecular alkylation reaction Journal of the Chemical Society-Perkin Transactions 1. 1305-1311. DOI: 10.1039/P19960001305 |
0.551 |
|
| 1996 |
Srikrishna A, Reddy TJ, Kumar PP. Synthesis of taxanes—the carvone approach; a simple, efficient stereo- and enantio-selective synthesis of the functionalised A ring Chemical Communications. 1369-1370. DOI: 10.1039/Cc9960001369 |
0.549 |
|
| 1996 |
Srikrishna A. A rapid way of computing the number of rings present in a polycyclic organic compound Journal of Chemical Education. 73: 428-428. DOI: 10.1021/Ed073P428 |
0.389 |
|
| 1996 |
Srikrishna A, Viswajanani R. Stereospecific construction of stereogenic vicinal quaternary carbon atoms. Enantiospecific synthesis of (+)-valerane☆ Tetrahedron Letters. 37: 2863-2864. DOI: 10.1016/0040-4039(96)00407-8 |
0.514 |
|
| 1996 |
Srikrishna A, Praveen Kumar P, Viswajanani R. A simple strategy for spirocyclopentannulation of cyclic ketones. Formal total synthesis of (±)-acorone Tetrahedron Letters. 37: 1683-1686. DOI: 10.1016/0040-4039(96)00109-8 |
0.594 |
|
| 1996 |
Srikrishna A, Reddy TJ, Nagaraju S. Enantioselective synthesis of both (+)- and (-)-derivatives of bicyclo[4.3.0]nonan-8-one and 3,8-diones from R-carvone Tetrahedron Letters. 37: 1679-1682. DOI: 10.1016/0040-4039(96)00106-2 |
0.557 |
|
| 1996 |
Srikrishna A, Reddy TJ, Viswajanani R. Reduction of quinolines to 1,2,3,4-tetrahydro derivatives employing a combination of NaCNBH3 and BF3.OEt2 Tetrahedron. 52: 1631-1636. DOI: 10.1016/0040-4020(95)00991-4 |
0.439 |
|
| 1995 |
Srikrishna A, Sattigeri JA, Viswajanani R, Yelamaggad CV. A Simple and Convenient One Step Method for the Reductive Deoxygenation of Aryl Ketones to Hydrocarbons Synlett. 1995: 93-94. DOI: 10.1055/S-1995-4866 |
0.495 |
|
| 1995 |
Srikrishna A, Viswajanani R. Tributylchlorostannane as Lewis Acid in the Regioselective Reductive Cleavage of Ketals Synlett. 1995: 95-96. DOI: 10.1055/S-1995-4863 |
0.432 |
|
| 1995 |
Srikrishna A, Krishnan K, Venkateswarlu S, Kumar PP. Isomerisation of 4-aryl-4-methylhex-5-en-2-ones to 5-aryl-4-methylhex-5-en-2-ones by an intramolecular ene-retro ene reaction sequence Journal of the Chemical Society-Perkin Transactions 1. 2033-2037. DOI: 10.1039/P19950002033 |
0.536 |
|
| 1995 |
Srikrishna A, Viswajanani R, Sattigeri JA. Cyclopentaannulation of allyl alcohols via a radical cyclisation reaction. Total synthesis of 4-epibakkenolide-A Journal of the Chemical Society, Chemical Communications. 469-470. DOI: 10.1039/C39950000469 |
0.518 |
|
| 1995 |
Srikrishna A, Viswajanani R, Sattigeri J, Vijaykumar D. A new, convenient reductive procedure for the deprotection of 4-methoxybenzyl (MPM) ethers to alcohols Journal of Organic Chemistry. 60: 5961-5962. DOI: 10.1021/Jo00123A038 |
0.43 |
|
| 1995 |
Srikrishna A, Sattigeri J, Viswajanani R, Yelamaggad C. Simple and Regioselective Reductive Cleavage of Tetrahydropyranyl Ethers to Alcohols Journal of Organic Chemistry. 60: 2260-2260. DOI: 10.1021/Jo00112A056 |
0.376 |
|
| 1995 |
Srikrishna A, Kumar P. Naphthalenes microwave irradiation induced rearrangement on montmorillonite K-10 Tetrahedron Letters. 36: 6313-6316. DOI: 10.1016/0040-4039(95)01219-8 |
0.337 |
|
| 1995 |
Srikrishna A, Viswajanani R, Sattigeri JA, Yelamaggad CV. Chemoselective reductive deoxygenation of α,β-unsaturated ketones and allyl alcohols Tetrahedron Letters. 36: 2347-2350. DOI: 10.1016/0040-4039(95)00252-8 |
0.434 |
|
| 1995 |
Srikrishna A, Viswajanani R, Yelamaggad CV. A new tetrahydrofurannulation via tandem radical cyclisation reaction-reductive deoxygenation sequence Tetrahedron Letters. 36: 1127-1128. DOI: 10.1016/0040-4039(94)02412-5 |
0.477 |
|
| 1995 |
Srikrishna A, Viswajanani R. A mild and simple procedure for the reductive cleavage of acetals and ketals Tetrahedron. 51: 3339-3344. DOI: 10.1016/0040-4020(95)00055-D |
0.46 |
|
| 1995 |
Srikrishna A, Nagaraju S, Kondaiah P. Application of microwave heating technique for rapid synthesis of γ,δ-unsaturated esters Tetrahedron. 51: 1809-1816. DOI: 10.1016/0040-4020(94)01058-8 |
0.453 |
|
| 1995 |
Srikrishna A, Nagaraju S. Regio-and stereospecific construction of vicinal quaternary carbons: Total synthesis of (±)-albene Phytochemistry. 40: 1699-1704. DOI: 10.1016/0031-9422(95)00592-U |
0.585 |
|
| 1994 |
Shankar MV, Varma KBR, Sharma GVR, Srikrishna A, Prasad BR, Subramaniam CK, Narayanan PS. Microstructural and non-linear optical properties of hot-pressed ethoxy methoxy chalcone (EMC) Ferroelectrics. 156: 141-146. DOI: 10.1080/00150199408215941 |
0.349 |
|
| 1994 |
Srikrishna A, Yelamaggad CV, Krishnan K, Nethaji M. First total synthesis of (±)-myltayl-4(12)-ene and single-crystal X-ray structure of exo-12-normyltaylan-4-yl 4-nitrobenzoate Journal of the Chemical Society, Chemical Communications. 2259-2260. DOI: 10.1039/C39940002259 |
0.432 |
|
| 1994 |
Srikrishna A, Hemamalini P, Venkateswarlu S. A regiospecific radical annulation strategy to functionalised chiral bicyclo[3.3.l]nonanes Tetrahedron. 50: 8781-8792. DOI: 10.1016/S0040-4020(01)85352-7 |
0.482 |
|
| 1994 |
Srikrishna A, Venkateswarlu S, Nagaraju S, Krishnan K. Isomerisation of 1-methylene-2-methyl-2-(2-oxopropyl)-cyclohexanes to 2-methylene-1-methyl-1-(2-oxopropyl)-cyclohexanes by ene and retro-ene reaction Tetrahedron. 50: 8765-8772. DOI: 10.1016/S0040-4020(01)85350-3 |
0.484 |
|
| 1994 |
Srikrishna A, Nagaraju S, Venkateswarlu S. A stereoselective synthesis of (±)-homogynolide-B Tetrahedron Letters. 35: 429-432. DOI: 10.1016/0040-4039(94)85072-0 |
0.51 |
|
| 1994 |
Srikrishna A, Reddy TJ, Nagaraju S, Sattigeri JA. A stereoselective total synthesis of bakkenolide-A (fukinanolide) Tetrahedron Letters. 35: 7841-7844. DOI: 10.1016/0040-4039(94)80132-0 |
0.54 |
|
| 1993 |
Srikrishna A, Krishnan K. Synthesis of (±)-thaps-7(15)-ene and (±)-thaps-6-enes Journal of the Chemical Society-Perkin Transactions 1. 667-673. DOI: 10.1039/P19930000667 |
0.532 |
|
| 1993 |
Srikrishna A, Nagaraju S, Sharma GVR. A radical cyclisation strategy to α-spiro-β-methylene-γ-butyrolactones. Total synthesis of (±)-norbakkenolide-A Journal of the Chemical Society, Chemical Communications. 285-288. DOI: 10.1039/C39930000285 |
0.482 |
|
| 1993 |
Srikrishna A, Krishnan K, Vankateswarlu S. Acid-catalysed thermal rearrangement of γ,δ-unsaturated ketones Journal of the Chemical Society, Chemical Communications. 143-145. DOI: 10.1039/C39930000143 |
0.464 |
|
| 1993 |
Srikrishna A, Hemamalini P, Sharma GVR. Chiral synthons from carvone. 9. Radical annulation strategy to chiral pupukeanones: total synthesis of (+)-10-exo-(1-naphthyl)pupukean-9-one and (+)-10-exo-(1-naphthyl)-5-epipupukean-9-ones Journal of Organic Chemistry. 58: 2509-2516. DOI: 10.1021/Jo00061A026 |
0.539 |
|
| 1992 |
Srikrishna A, Nagaraju S, Sharma GVR. Sonochemical Acceleration of Conversion of 2-Alkoxytetrahydrofurans to γ-Butyrolactones Synthesis of (±)-Quercus Lactone-A Synthetic Communications. 22: 1127-1135. DOI: 10.1080/00397919208021096 |
0.543 |
|
| 1992 |
Srikrishna A, Sharma GV, Nagaraju S. Chiral Synthons from Monoterpenes.1Stereoselective Syntheses of (-)5S, 6S, 9R-6-Isopropyl-9-Methyl-2-Oxaspiro[4.4]Nonan-3-One and (-) 3aR, 6R, 7aR-3a-Methyl-6-Isopropenylhexahydrobenzofuran-2-One Synthetic Communications. 22: 1221-1230. DOI: 10.1080/00397919208019303 |
0.478 |
|
| 1992 |
Srikrishna A, Nagaraju S. Acceleration of ortho ester Claisen rearrangement by a commercial microwave oven Journal of the Chemical Society-Perkin Transactions 1. 311-312. DOI: 10.1039/P19920000311 |
0.449 |
|
| 1992 |
Srikrishna A, Hemmalini P. Radical cyclisation strategies to bridged systems. Regioselective construction of chiral bicyclo [2.2.2] and [3.2.1] octanes via 6-exo trig and 5-exo trig radical cyclisation reactions Tetrahedron. 48: 9337-9354. DOI: 10.1016/S0040-4020(01)85623-4 |
0.489 |
|
| 1992 |
Srikrishna A, Krishnan K, Yelamaggad CV. Regiocontrol in the cyclopropane ring cleavage of tricyclo[4.4.0.01,3]decanes to hydrindane and decalin systems Tetrahedron. 48: 9725-9734. DOI: 10.1016/S0040-4020(01)81189-3 |
0.411 |
|
| 1992 |
Srikrishna A, Krishnan K. Total synthese of (±)-cyclolaurene, (±)-epicylolaurene and (±)-β-cuparenones Tetrahedron. 48: 3429-3436. DOI: 10.1016/0040-4020(92)85016-8 |
0.476 |
|
| 1991 |
Srikrishna A, Nagaraju S. Stereospecific total synthesis of (±)-albene via a prochiral precursor Journal of the Chemical Society-Perkin Transactions 1. 657-658. DOI: 10.1039/P19910000657 |
0.61 |
|
| 1991 |
Srikrishna A, Krishnan K. First total synthesis of a natural thapsane Journal of the Chemical Society, Chemical Communications. 1693-1694. DOI: 10.1039/C39910001693 |
0.55 |
|
| 1991 |
Srikrishna A, Sundarababu G. Radical cyclization strategies to terpenoids; syntheses of (±)-β-cuparenone, (±)-laurene and epilaurenes Tetrahedron. 47: 481-496. DOI: 10.1016/S0040-4020(01)90504-6 |
0.536 |
|
| 1991 |
Srikrishna A, Hemamalini P, Sharma GVR. A regio and stereospecific radical annulation route to chiral tricyclo[4.3.1.o3,7]decane (isotwistane) system1 synthesis of (+)-10-α-Naphthyl-5-epi-Pupukean-9-one Tetrahedron Letters. 32: 6609-6610. DOI: 10.1016/0040-4039(91)80234-W |
0.478 |
|
| 1990 |
Srikrishna A. Synthesis of Hexacyclo [6.5.1.02,7.03,11.04,9.010,14] Tetradeca-5, 12-diene Synthetic Communications. 20: 279-284. DOI: 10.1080/00397919008052295 |
0.545 |
|
| 1990 |
Srikrishna A, Sharma GVR, Hemamalini P. Cyclopropanes via an efficient 3-exo trig radical cyclisation reaction Journal of the Chemical Society, Chemical Communications. 1681-1683. DOI: 10.1039/C39900001681 |
0.474 |
|
| 1990 |
Srikrishna A, Hemamalini P. Chiral synthons from carvone. Part 4. Radical cyclization strategies to bridged systems. Synthesis of bicyclo[3.2.1]octan-3-ones from (S)-carvone Journal of Organic Chemistry. 55: 4883-4887. DOI: 10.1021/Jo00303A023 |
0.43 |
|
| 1990 |
Srikrishna A, Sundarababu G. A radical cyclisation reaction based strategy to 2,3,5-tri- and tetrasubstituted furans Tetrahedron. 46: 7901-7910. DOI: 10.1016/S0040-4020(01)90088-2 |
0.469 |
|
| 1990 |
Srikrishna A, Sundarababu G. A radical cyclisation based strategy to cuparenoids; synthesis of (±)-α-cuparenone, (±)-epilaurene and laurenes Tetrahedron. 46: 3601-3606. DOI: 10.1016/S0040-4020(01)81528-3 |
0.489 |
|
| 1990 |
SRIKRISHNA A, SHARMA GVR. ChemInform Abstract: A Simple, One Pot, Regiospecific 1,3-Dicarboxy Benzannulation of Active Acyl Systems. Cheminform. 21. DOI: 10.1002/CHIN.199007176 |
0.276 |
|
| 1990 |
SRIKRISHNA A, SHARMA GVR. ChemInform Abstract: A Simple Synthesis of (.+-.)-Evodone Cheminform. 21. DOI: 10.1002/chin.199006275 |
0.484 |
|
| 1989 |
Srikrishna A, Hemamalini P. Bridged systems via radical cyclisations: synthesis of chiral bicyclo[3.3.1]nonanes by sequential inter- and intra-molecular radical Michael addition Journal of the Chemical Society-Perkin Transactions 1. 2511-2513. DOI: 10.1039/P19890002511 |
0.507 |
|
| 1989 |
Srikrishna A, Krishnan K. Synthesis of (.+-.)-marmelo oxides by a radical cyclization reaction Journal of Organic Chemistry. 54: 3981-3983. DOI: 10.1021/Jo00277A043 |
0.492 |
|
| 1989 |
Srikrishna A, Krishnan K. Stereospecific Synthesis of Thaps-7(15)-ene and thaps-6-ene, Probable Biogenetic Precursors of Thapsanes Tetrahedron Letters. 30: 6577-6580. DOI: 10.1016/S0040-4039(01)89026-2 |
0.575 |
|
| 1989 |
Srikrishna A, Sunderbabu G. Total synthesis of (±)-laurene and epilaurene by radical cyclisation reaction Tetrahedron Letters. 30: 3561-3562. DOI: 10.1016/S0040-4039(00)99440-1 |
0.532 |
|
| 1989 |
SRIKRISHNA A, SHARMA GVR. ChemInform Abstract: A Radical Cyclization Route to (.+-.)-Andirolactone (VIII), a Spiro-γ-butyrolactone. Cheminform. 20. DOI: 10.1002/CHIN.198924154 |
0.369 |
|
| 1988 |
Srikrishna A, Sunderbabu G. A radical cyclisation route to 3-alkyl furans. Synthesis of perillene and dendrolasin. Chemistry Letters. 17: 371-372. DOI: 10.1246/Cl.1988.371 |
0.547 |
|
| 1988 |
Srikrishna A, Krishnan K. A strategy to 3-acyl-4-methyl furans. Synthesis of (±)-evodone Tetrahedron Letters. 29: 4995-4996. DOI: 10.1016/S0040-4039(00)80662-0 |
0.555 |
|
| 1987 |
Srikrishna A. A radical cyclisation route to α-methylene-γ-butyrolactones Journal of the Chemical Society, Chemical Communications. 587-588. DOI: 10.1039/C39870000587 |
0.466 |
|
| 1987 |
Mehta G, Srikrishna A, Rao KS, Reddy KR, Acharya KA, Puranik VG, Tavale SS, Row TNG. Novel polyquinanes from a caged hexacyclic [4.4.2]propellane system Journal of Organic Chemistry. 52: 457-460. DOI: 10.1021/Jo00379A031 |
0.582 |
|
| 1987 |
Srikrishna A, Sunderbabu G. Hexacyclo[6.6.1.02,7.03,12.06,11.09,14]pentadecane and pentacyclo[8.4.0.03,8.03,14.07,11]tetradecane systems from decahydro[1,4;5,8]dimethanoanthracene-11,12-dione Journal of Organic Chemistry. 52: 5037-5039. DOI: 10.1021/Jo00231A041 |
0.31 |
|
| 1987 |
Srikrishna A, Sunderbabu G. A simple synthesis of 2,3-disubstituted purans Tetrahedron Letters. 28: 6393-6394. DOI: 10.1016/S0040-4039(01)91383-8 |
0.576 |
|
| 1987 |
Srikrishna A, Pullaiah KC. Furannulation via radical cyclisation Tetrahedron Letters. 28: 5203-5204. DOI: 10.1016/S0040-4039(00)95629-6 |
0.44 |
|
| 1986 |
Mehta G, Reddy AV, Srikrishna A. Synthesis and rearrangements of the pentacyclo[5.4.0.0.0.0]undecane [1,2,4-trishomocubane] ring system Journal of the Chemical Society-Perkin Transactions 1. 17: 291-297. DOI: 10.1039/P19860000291 |
0.608 |
|
| 1984 |
Eaton PE, Srikrishna A, Uggeri F. Cyclopentannulation of bicyclo[3.3.0]octane-3,7-dione. A more convenient synthesis of the [5]peristylane system Journal of Organic Chemistry. 49: 1728-1732. DOI: 10.1021/Jo00184A012 |
0.523 |
|
| 1984 |
Eaton PE, Srikrishna A, Uggeri F. Cyclopentannulation Of Bicyclo(3.3.0)Octane-3,7-Dione. A More Convenient Synthesis Of The (5)Peristylane System Cheminform. 15. DOI: 10.1002/Chin.198448145 |
0.695 |
|
| 1984 |
Mehta G, Nair MS, Srikrishna A. A Synthetic Approach To Pentacyclo(6.4.0.03,11.06,10.09,12)Dodecane System Cheminform. 15. DOI: 10.1002/Chin.198410102 |
0.575 |
|
| 1983 |
Mehta G, Srikrishna A, Suri SC, Nair MS. Tetracyclo[5.4.0.03,10.04,8]undecane (2,9-ethanonoradamantane) and 12-oxapentacyclo[6.4.0.02,6.03,11.04,9]dodecane system The Journal of Organic Chemistry. 48: 5107-5109. DOI: 10.1021/Jo00173A060 |
0.544 |
|
| 1982 |
Mehta G, Srikrishna A. Decahydro-1,3,5-methenocyclopenta[cd]pentalene (trishomocubane) framework: novel photochemical synthesis, acid-catalysed cyclo-reversion, and possible role as a solar energy storage system Journal of the Chemical Society, Chemical Communications. 218-219. DOI: 10.1039/C39820000218 |
0.62 |
|
| 1981 |
Mehta G, Srikrishna A. A novel rearrangement of tricyclo[4.2.2.02,5]deca-3,7-dien-9-ones to functionalized bicyclo[3.2.1]octa-2,6-dienes Journal of Organic Chemistry. 46: 1730-1732. DOI: 10.1021/Jo00321A043 |
0.618 |
|
| 1981 |
Mehta G, Srikrishna A, Reddy AV, Nair MS. A novel, versatile synthetic approach to linearly fused tricyclopentanoids via photo-thermal olefin metathesis Tetrahedron. 37: 4543-4559. DOI: 10.1016/0040-4020(81)80021-X |
0.6 |
|
| 1981 |
MEHTA G, SRIKRISHNA A. ChemInform Abstract: A NOVEL REARRANGEMENT OF TRICYCLO(4.2.2.02,5)DECA-3,7-DIEN-9-ONES TO FUNCTIONALIZED BICYCLO(3.2.1)OCTA-2,6-DIENES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198138257 |
0.634 |
|
| 1981 |
MEHTA G, SRIKRISHNA A, SURI SC. ChemInform Abstract: CONVENIENT PREPARATIVE ROUTES TO 1,8-BISHOMOCUBANE, 1,8-BISHOMOCUBANONE, SNOUTANONE, AND HOMOCUBANONE Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198119159 |
0.633 |
|
| 1980 |
Mehta G, Srikrishna A, Suri SC. Convenient preparative routes to 1,8-bishomocubane, 1,8-bishomocubanone, snoutanone, and homocubanone Journal of Organic Chemistry. 45: 5375-5377. DOI: 10.1021/Jo01314A035 |
0.625 |
|
| 1979 |
Mehta G, Srikrishna A. Photochemistry of tricyclo [4.2.2.02,5] deca-3,7-dien-9-one: a source of many interesting polycycles Tetrahedron Letters. 20: 3187-3190. DOI: 10.1016/S0040-4039(01)95358-4 |
0.67 |
|
| 1979 |
Mehta G, Reddy AV, Srikrishna A. Olefin metathesis in polycyclic frames 1. A new way to , , - tricyclopentanoids (acs-C11-triquinanes) Tetrahedron Letters. 20: 4863-4866. DOI: 10.1016/S0040-4039(01)86734-4 |
0.618 |
|
| 1979 |
Mehta G, Singh V, Srikrishna A, Stanley Cameron T, Chan C. Polycyclic rearrangements. A novel, carbonium ion mediated, bicyclo (4.2.0) octa-2,4-diene→1,3,5-cyclooctatriene isomerisation in a propellane framework Tetrahedron Letters. 20: 4595-4598. DOI: 10.1016/S0040-4039(01)86659-4 |
0.716 |
|
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