| Year |
Citation |
Score |
| 2024 |
Chintalapudi V, Wilson C, Clark JS. Synthesis of the I-K Fused Polyether Array of CTX3C and Related Ciguatoxins by Use of a Gold-Catalyzed Cyclization Reaction. Organic Letters. PMID 38238251 DOI: 10.1021/acs.orglett.3c03782 |
0.703 |
|
| 2023 |
Triantafyllakis M, Alexander S, Woolford S, Wilson C, Clark JS. Synthesis of the A-F Fragment of the Pacific Ciguatoxin CTX3C by Iterative Ring-Closing Metathesis and Tsuji-Trost Allylation. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303121. PMID 37830907 DOI: 10.1002/chem.202303121 |
0.379 |
|
| 2022 |
Decultot L, Clark JS. Synthetic Studies on Amphidinolide F: Exploration of Macrocycle Construction by Intramolecular Stille Coupling. Organic Letters. 24: 7600-7604. PMID 36223230 DOI: 10.1021/acs.orglett.2c03045 |
0.391 |
|
| 2022 |
Romiti F, Decultot L, Clark JS. Convergent Synthesis of the C1-C29 Framework of Amphidinolide F. The Journal of Organic Chemistry. 87: 8126-8141. PMID 35675580 DOI: 10.1021/acs.joc.2c00850 |
0.34 |
|
| 2020 |
Clark JS, Popadynec M. Stereoselective Synthesis of the I-L Fragment of the Pacific Ciguatoxins. Toxins. 12. PMID 33255410 DOI: 10.3390/toxins12120740 |
0.422 |
|
| 2020 |
Popadynec M, Gibbard H, Clark JS. Bidirectional Synthesis of the IJK Fragment of Ciguatoxin CTX3C by Sequential Double Ring-Closing Metathesis and Tsuji-Trost Allylation. Organic Letters. PMID 32306737 DOI: 10.1021/Acs.Orglett.0C01238 |
0.541 |
|
| 2019 |
Clark JS, Campbell A, Mat Som I, Wilson C. Total Syntheses of 11-Acetoxy-4-deoxyasbestinin D, 4-Deoxyasbestinin C, Asbestinin-10, -20, -21 and -23. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31710141 DOI: 10.1002/Chem.201904998 |
0.379 |
|
| 2019 |
Aimon A, Farrugia LJ, Clark JS. Synthesis of the Core Framework of the Cornexistins by Intramolecular Nozaki-Hiyama-Kishi Coupling. Molecules (Basel, Switzerland). 24. PMID 31336669 DOI: 10.3390/Molecules24142654 |
0.534 |
|
| 2019 |
Elustondo F, Chintalapudi V, Clark JS. A Short Sequence for the Iterative Synthesis of Fused Polyethers Helvetica Chimica Acta. 102. DOI: 10.1002/Hlca.201900161 |
0.538 |
|
| 2019 |
Qin S, Cao Y, Luo Y, Jiang S, Clark JS, Wang X, Yang G. Multi‐Gram Scale Synthesis of Chiral 3‐Methyl‐2,5‐trans‐tetrahydrofurans Helvetica Chimica Acta. 102. DOI: 10.1002/Hlca.201900131 |
0.577 |
|
| 2018 |
Klaus V, Wittmann S, Senn HM, Clark JS. Synthesis of fused tricyclic systems by thermal Cope rearrangement of furan-substituted vinyl cyclopropanes. Organic & Biomolecular Chemistry. PMID 29761822 DOI: 10.1039/C8Ob00924D |
0.51 |
|
| 2018 |
Skardon-Duncan J, Sparenberg M, Bayle A, Alexander S, Clark JS. Stereoselective Synthesis of Medium-Sized Cyclic Ethers by Sequential Ring-Closing Metathesis and Tsuji-Trost Allylation. Organic Letters. PMID 29676923 DOI: 10.1021/Acs.Orglett.8B01082 |
0.498 |
|
| 2017 |
Xu C, Wittmann S, Gemander M, Ruohonen V, Clark JS. Trialkylphosphine-Mediated Synthesis of 2-Acyl Furans from Ynenones. Organic Letters. PMID 28654294 DOI: 10.1021/Acs.Orglett.7B01533 |
0.541 |
|
| 2017 |
Clark JS, McAulay K. Total Synthesis of 7-epi-Pukalide and 7-Acetylsinumaximol B. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28594456 DOI: 10.1002/Chem.201702591 |
0.478 |
|
| 2017 |
Klaus V, Clark JS. Thioether-Catalysed Tandem Synthesis of Furans and Cyclic Ethers or Lactones Synlett. 28: 1358-1362. DOI: 10.1055/S-0036-1588758 |
0.517 |
|
| 2016 |
Clark JS, Xu C. Total Synthesis of (-)-Nakadomarin A. Angewandte Chemie (International Ed. in English). PMID 26923079 DOI: 10.1002/Anie.201600990 |
0.604 |
|
| 2015 |
Clark JS, Romiti F, Sieng B, Paterson LC, Stewart A, Chaudhury S, Thomas LH. Synthesis of the A-D Ring System of the Gambieric Acids. Organic Letters. 17: 4694-7. PMID 26367818 DOI: 10.1021/Acs.Orglett.5B02093 |
0.533 |
|
| 2015 |
Clark JS, Romiti F, Hogg KF, Hamid MH, Richter SC, Boyer A, Redman JC, Farrugia LJ. Synthesis of cyclopropyl-substituted furans by brønsted Acid promoted cascade reactions. Angewandte Chemie (International Ed. in English). 54: 5744-7. PMID 25782604 DOI: 10.1002/Anie.201500625 |
0.778 |
|
| 2015 |
Clark JS, Delion L, Farrugia LJ. Synthesis of four diastereomers of sclerophytin F and structural reassignment of several sclerophytin natural products. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 4772-80. PMID 25663662 DOI: 10.1002/Chem.201406051 |
0.328 |
|
| 2015 |
Gray ST, Herr MW, Sethi RK, Diercks G, Lee L, Curry W, Chan A, Clark J, Holbrook EH, Rocco J, Sadow PM, Lin DT. Treatment outcomes and prognostic factors, including human papillomavirus, for sinonasal undifferentiated carcinoma: a retrospective review. Head & Neck. 37: 366-74. PMID 24421248 DOI: 10.1002/Hed.23606 |
0.01 |
|
| 2015 |
Mesquita LMM, Pinto RMA, Salvador JAR, Clark JH, Budarin VL. Starbon®400-HSO3: A green mesoporous carbonaceous solid acid catalyst for the Ritter reaction Catalysis Communications. 69: 170-173. DOI: 10.1016/J.Catcom.2015.06.010 |
0.305 |
|
| 2014 |
Clark JS, Delion L, Farrugia LJ. Total synthesis of the purported structure of sclerophytin F. Organic Letters. 16: 4300-3. PMID 25068316 DOI: 10.1021/Ol5020152 |
0.41 |
|
| 2014 |
Clark JS, Hansen KE. Intramolecular reactions of metal carbenoids with allylic ethers: is a free ylide involved in every case? Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 5454-9. PMID 24648216 DOI: 10.1002/Chem.201304054 |
0.463 |
|
| 2013 |
Clark JS, Yang G, Osnowski AP. Synthesis of the C-1-C-17 fragment of amphidinolides C, C2, C3, and F. Organic Letters. 15: 1460-3. PMID 23527702 DOI: 10.1021/Ol4004838 |
0.303 |
|
| 2013 |
Clark JS, Yang G, Osnowski AP. Synthesis of the C-18-C-34 fragment of amphidinolides C, C2, and C3. Organic Letters. 15: 1464-7. PMID 23527614 DOI: 10.1021/Ol400482J |
0.317 |
|
| 2013 |
Clark JS, Berger R, Hayes ST, Senn HM, Farrugia LJ, Thomas LH, Morrison AJ, Gobbi L. Total syntheses of multiple cladiellin natural products by use of a completely general strategy. The Journal of Organic Chemistry. 78: 673-96. PMID 23215006 DOI: 10.1021/Jo302542H |
0.562 |
|
| 2012 |
Clark JS, Boyer A, Aimon A, Engel García P, Lindsay DM, Symington AD, Danoy Y. Organocatalytic synthesis of highly substituted furfuryl alcohols and amines. Angewandte Chemie (International Ed. in English). 51: 12128-31. PMID 23097350 DOI: 10.1002/Anie.201207300 |
0.78 |
|
| 2011 |
Clark JS, Vignard D, Parkin A. Synthesis of the tricyclic core of labiatin A and australin A. Organic Letters. 13: 3980-3. PMID 21732661 DOI: 10.1021/ol201498g |
0.5 |
|
| 2011 |
Clark JS, Labre F, Thomas LH. Concise synthesis of the C-1-C-12 fragment of amphidinolides T1-T5. Organic & Biomolecular Chemistry. 9: 4823-30. PMID 21509362 DOI: 10.1039/C1Ob05130J |
0.461 |
|
| 2010 |
Clark JS, Berger R, Hayes ST, Thomas LH, Morrison AJ, Gobbi L. Enantioselective total syntheses of three cladiellins (eunicellins): a general approach to the entire family of natural products. Angewandte Chemie (International Ed. in English). 49: 9867-70. PMID 21082639 DOI: 10.1002/Anie.201005508 |
0.321 |
|
| 2010 |
Clark JS, Elustondo F, Trevitt GP, Boyall D, Robertson J, Blake AJ, Wilson C, Stammen B. ChemInform Abstract: Preparation of Cyclic Ethers for Polyether Synthesis by Catalytic Ring-Closing Enyne Metathesis of Alkynyl Ethers. Cheminform. 33: no-no. DOI: 10.1002/chin.200230258 |
0.478 |
|
| 2010 |
Clark JS, Hodgson PB, Goldsmith MD, Blake AJ, Cooke PA, Street LJ. ChemInform Abstract: Rearrangement of Ammonium Ylides Produced by Intramolecular Reaction of Catalytically Generated Metal Carbenoids. Part 2. Stereoselective Synthesis of Bicyclic Amines. Cheminform. 33: no-no. DOI: 10.1002/chin.200215124 |
0.425 |
|
| 2010 |
Wilson C, Clark JS, Bate AL, Blake AJ, Grinter T, Teat SJ. ChemInform Abstract: Diels-Alder Adducts of Medium-Ring Carbocyclic Dienes Prepared by Rearrangement of Catalytically Generated Cyclic Oxonium Ylides Cheminform. 33: no-no. DOI: 10.1002/chin.200209022 |
0.42 |
|
| 2010 |
Clark JS, Townsend RJ, Blake AJ, Teat SJ, Johns A. ChemInform Abstract: A Concise Enantioselective Synthesis of the AB Ring System of the Manzamine Alkaloids by Ring-Closing Enyne Metathesis. Cheminform. 32: no-no. DOI: 10.1002/chin.200129189 |
0.425 |
|
| 2010 |
BURTON JW, CLARK JS, DERRER S, STORK TC, BENDALL JG, HOLMES AB. ChemInform Abstract: Synthesis of Medium Ring Ethers. Part 5. The Synthesis of (+)- Laurencin Cheminform. 28: no-no. DOI: 10.1002/chin.199750249 |
0.598 |
|
| 2010 |
CLARK JS, KETTLE JG. ChemInform Abstract: Synthesis of Brevetoxin Sub-Units by Sequential Ring-Closing Metathesis and Hydroboration. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199716270 |
0.362 |
|
| 2010 |
ROBINSON RA, CLARK JS, HOLMES AB. ChemInform Abstract: Synthesis of (+)-Laurencin. Cheminform. 25: no-no. DOI: 10.1002/chin.199407271 |
0.55 |
|
| 2010 |
EVANS DA, NG HP, CLARK JS, RIEGER DL. ChemInform Abstract: Diastereoselective anti Aldol Reactions of Chiral Ethyl Ketones. Enantioselective Processes for the Synthesis of Polypropionate Natural Products. Cheminform. 23: no-no. DOI: 10.1002/chin.199230094 |
0.438 |
|
| 2010 |
CARLING RW, CLARK JS, HOLMES AB, SARTOR D. ChemInform Abstract: Synthesis of Medium Ring Ethers. Part 13. Disproof of the Proposed 2,8- Disubstituted Oxocane Structure for Gloeosporone. Synthesis of pseudo- Gloeosporone. Cheminform. 23: no-no. DOI: 10.1002/chin.199216321 |
0.573 |
|
| 2010 |
CARLING RW, CLARK JS, HOLMES AB. ChemInform Abstract: Synthesis of Medium Ring Ethers. Part 2. Synthesis of the Fully Saturated Carbon Skeleton of Laurencia Non-Terpenoid Ether Metabolites Containing Seven-, Eight- and Nine-Membered Rings. Cheminform. 23: no-no. DOI: 10.1002/chin.199215300 |
0.563 |
|
| 2008 |
Clark JS, Northall JM, Marlin F, Nay B, Wilson C, Blake AJ, Waring MJ. Synthetic studies on the cornexistins: synthesis of (+/-)-5-epi-hydroxycornexistin. Organic & Biomolecular Chemistry. 6: 4012-25. PMID 18931810 DOI: 10.1039/B811245B |
0.5 |
|
| 2008 |
Clark JS, Baxter CA, Dossetter AG, Poigny S, Castro JL, Whittingham WG. Stereoselective construction of the tricyclic core of neoliacinic acid. The Journal of Organic Chemistry. 73: 1040-55. PMID 18171077 DOI: 10.1021/Jo702111U |
0.487 |
|
| 2008 |
Clark JS, Guerot C, Wilson C, Blake AJ. ChemInform Abstract: Rapid Synthesis of Medium-Ring Fused Polycarbocyclic Systems by Rearrangement of Carbenoid-Derived Oxonium Ylides. Cheminform. 39. DOI: 10.1002/chin.200809113 |
0.396 |
|
| 2007 |
Clark JS, Guérot C, Wilson C, Blake AJ. Rapid synthesis of medium-ring fused polycarbocyclic systems by rearrangement of carbenoid-derived oxonium ylides. Chemical Communications (Cambridge, England). 4134-6. PMID 17925953 DOI: 10.1039/B709064A |
0.443 |
|
| 2007 |
Clark JS, Conroy J, Blake AJ. Rapid synthesis of the A-E fragment of ciguatoxin CTX3C. Organic Letters. 9: 2091-4. PMID 17465560 DOI: 10.1021/ol0706096 |
0.422 |
|
| 2007 |
Clark JS, Grainger DM, Ehkirch AA, Blake AJ, Wilson C. Synthesis of the fused polyether core of hemibrevetoxin B by two-directional ring-closing metathesis. Organic Letters. 9: 1033-6. PMID 17311391 DOI: 10.1021/Ol0630651 |
0.548 |
|
| 2007 |
Clark JS, Hayes ST, Wilson C, Gobbi L. A concise total synthesis of (+/-)-vigulariol. Angewandte Chemie (International Ed. in English). 46: 437-40. PMID 17146807 DOI: 10.1002/CHIN.200717177 |
0.422 |
|
| 2007 |
Clark JS, Hayes ST, Blake AJ, Gobbi L. Synthesis of a lactone natural product found in Greek tobacco Tetrahedron Letters. 48: 2501-2503. DOI: 10.1016/J.Tetlet.2007.02.039 |
0.378 |
|
| 2006 |
Clark JS. Construction of fused polycyclic ethers by strategies involving ring-closing metathesis. Chemical Communications (Cambridge, England). 3571-81. PMID 17047770 DOI: 10.1039/B601839D |
0.527 |
|
| 2006 |
Clark J, Winfield L, Wilson C, Blake A. Synthetic Studies on the Cladiellins (Eunicellins): Unexpected Selenoxide Displacement with Concomitant Alcohol Oxidation During Attempted Selenoxide Elimination Synlett. 2006: 2191-2194. DOI: 10.1055/S-2006-949611 |
0.384 |
|
| 2006 |
Clark JS, Fessard TC, Whitlock GA. A concise enantioselective synthesis of the fungal metabolite (+)-decarestrictine L Tetrahedron. 62: 73-78. DOI: 10.1016/J.Tet.2005.09.144 |
0.43 |
|
| 2006 |
Clark JS, Walls SB, Wilson C, East SP, Drysdale MJ. Construction of fused medium-ring carbocycles by catalytic generation and rearrangement of oxonium ylides European Journal of Organic Chemistry. 323-327. DOI: 10.1002/Ejoc.200500830 |
0.508 |
|
| 2005 |
Clark JS, Roche C. Tuneable asymmetric copper-catalysed allylic amination and oxidation reactions. Chemical Communications (Cambridge, England). 5175-7. PMID 16228026 DOI: 10.1039/B509678B |
0.444 |
|
| 2005 |
Clark JS, Kimber MC, Robertson J, McErlean CS, Wilson C. Rapid two-directional synthesis of the F-J fragment of the gambieric acids by iterative double ring-closing metathesis. Angewandte Chemie (International Ed. in English). 44: 6157-62. PMID 16134189 DOI: 10.1002/Anie.200501925 |
0.438 |
|
| 2005 |
Clark J, Roche C. Asymmetric Copper-Catalyzed Allylic Amination and Oxidation Reactions Synfacts. 2006: 0037-0037. DOI: 10.1055/S-2005-921742 |
0.327 |
|
| 2005 |
Clark JS, Baxter CA, Castro JL. Synthesis of the Tricyclic Core of the Marine Natural Product Labiatin A Synthesis. 2005: 3398-3404. DOI: 10.1055/S-2005-918485 |
0.5 |
|
| 2005 |
Clark JS, Myatt J, Roberts L, Walshe N. Investigation of the biomimetic synthesis of emindole SB using a fluorinated polyene cyclisation precursor Synlett. 2005: 697-699. DOI: 10.1055/S-2005-863721 |
0.51 |
|
| 2004 |
Clark JS, Elustondo F, Kimber MC. Construction of building-blocks for polyether synthesis using sequential catalytic ring-closing enyne and cross metathesis. Chemical Communications (Cambridge, England). 2470-1. PMID 15514820 DOI: 10.1039/B409067E |
0.463 |
|
| 2004 |
Clark JS, Dossetter AG, Wong YS, Townsend RJ, Whittingham WG, Russell CA. Anomalous intramolecular C-H insertion reactions of rhodium carbenoids: factors influencing the reaction course and mechanistic implications. The Journal of Organic Chemistry. 69: 3886-98. PMID 15153022 DOI: 10.1021/Jo049900E |
0.371 |
|
| 2004 |
Clark JS, Fessard TC, Wilson C. A concise and stereoselective synthesis of the A-ring fragment of the gambieric acids. Organic Letters. 6: 1773-6. PMID 15151411 DOI: 10.1021/Ol049483S |
0.572 |
|
| 2004 |
Clark JS, Clarke M, Clough J, Blake AJ, Wilson C. Asymmetric allylic oxidation of bridged-bicyclic alkenes using a copper-catalysed symmetrising–desymmetrising Kharasch–Sosnovsky reaction Tetrahedron Letters. 45: 9447-9450. DOI: 10.1016/J.Tetlet.2004.10.093 |
0.463 |
|
| 2004 |
Clark JS, Freeman RP, Cacho M, Thomas AW, Swallow S, Wilson C. Stereoselective synthesis of the cyclic ether core of (+)-laurenyne Tetrahedron Letters. 45: 8639-8642. DOI: 10.1016/J.Tetlet.2004.09.160 |
0.548 |
|
| 2003 |
Clark JS, Whitlock G, Jiang S, Onyia N. Stereoselective synthesis of tetrahydropyran-3-ones by rearrangement of oxonium ylides generated from metal carbenoids. Chemical Communications (Cambridge, England). 2578-9. PMID 14594289 DOI: 10.1039/B307858M |
0.471 |
|
| 2003 |
Clark JS, Myatt J, Wilson C, Roberts L, Walshe N. Exploration of the biomimetic synthesis of indole-diterpene mycotoxins: an unexpected cascade reaction during the attempted synthesis of emindole SB. Chemical Communications (Cambridge, England). 1546-7. PMID 12868746 DOI: 10.1039/B302105J |
0.561 |
|
| 2003 |
Clark JS, Marlin F, Nay B, Wilson C. Synthesis of the carbocyclic core of the cornexistins by ring-closing metathesis. Organic Letters. 5: 89-92. PMID 12509898 DOI: 10.1021/ol027265y |
0.466 |
|
| 2003 |
Clark JS, Middleton MD. Direct peptide coupling of novel amino acid derivatives produced by rearrangement of catalytically generated ammonium ylides Tetrahedron Letters. 44: 7031-7034. DOI: 10.1016/S0040-4039(03)01778-7 |
0.417 |
|
| 2001 |
Clark JS, Hodgson PB, Goldsmith MD, Blake AJ, Cooke PA, Street LJ. Rearrangement of ammonium ylides produced by intramolecular reaction of catalytically generated metal carbenoids. Part 2. Stereoselective synthesis of bicyclic amines Journal of the Chemical Society-Perkin Transactions 1. 3325-3337. DOI: 10.1039/B108182A |
0.538 |
|
| 2001 |
Clark JS, Hodgson PB, Goldsmith MD, Street LJ. Rearrangement of ammonium ylides produced by intramolecular reaction of catalytically generated metal carbenoids. Part 1. Synthesis of cyclic amines Journal of the Chemical Society-Perkin Transactions 1. 3312-3324. DOI: 10.1039/B108179A |
0.576 |
|
| 2001 |
Clark JS, Bate AL, Grinter T. A novel approach to the construction of medium-ring carbocycles utilising the rearrangement of oxonium ylides generated from metal carbenoids Chemical Communications. 459-460. DOI: 10.1039/B100292I |
0.466 |
|
| 2001 |
Clark JS, Wong Y, Townsend RJ. Probing the mechanism of the anomalous intramolecular C-H insertion reaction of rhodium carbenoids by analysis of kinetic isotope effects Tetrahedron Letters. 42: 6187-6190. DOI: 10.1016/S0040-4039(01)01173-X |
0.423 |
|
| 2001 |
Clark J, Townsend RJ, Blake AJ, Teat SJ, Johns A. A concise enantioselective synthesis of the AB ring system of the manzamine alkaloids by ring-closing enyne metathesis Tetrahedron Letters. 42: 3235-3238. DOI: 10.1016/S0040-4039(01)00404-X |
0.531 |
|
| 2000 |
Clark JS, Hamelin O. Synthesis of Polycyclic Ethers by Two-Directional Double Ring-Closing Metathesis. Angewandte Chemie. 39: 372-374. PMID 10649414 DOI: 10.1002/(Sici)1521-3773(20000117)39:2<372::Aid-Anie372>3.0.Co;2-Y |
0.547 |
|
| 2000 |
Clark JS, Wong Y. Construction of the 11-oxabicyclo[6.2.1]undecane core of the cladiellins by a novel rearrangement reaction Chemical Communications. 1079-1080. DOI: 10.1039/B002511I |
0.499 |
|
| 1999 |
Clark JS, Dossetter AG, Blake AJ, Li W, Whittingham WG. Synthesis of the functionalised core of neoliacinic acid Chemical Communications. 749-750. DOI: 10.1039/A901711I |
0.413 |
|
| 1999 |
Clark JS, Kettle JG. Synthesis of Sub-units of Marine Polycyclic Ethers by Ring-closing Metathesis and Hydroboration of Enol Ethers Tetrahedron. 55: 8231-8248. DOI: 10.1016/S0040-4020(99)00303-8 |
0.523 |
|
| 1998 |
Clark JS. Book Review, Named Organic Reaction Synthesis. 1998: 1558. DOI: 10.1055/S-1998-4524 |
0.313 |
|
| 1998 |
Clark JS, Trevitt GP, Boyall D, Stammen B. Synthesis of alkenyl-substituted cyclic enol ethers by catalytic ring-closing metathesis of alkynyl ethers Chemical Communications. 2629-2630. DOI: 10.1039/A807667G |
0.561 |
|
| 1998 |
Clark JS, Tolhurst KF, Taylor M, Swallow S. Enantioselective allylic acyloxylation catalysed by copper–oxazoline† complexes Journal of the Chemical Society-Perkin Transactions 1. 1167-1170. DOI: 10.1039/A801238E |
0.393 |
|
| 1998 |
Clark JS, Hamelin O, Hufton R. Synthesis of medium-sized cyclic allylic ethers by ring-closing metathesis and subsequent elaboration to sub-units found in the brevetoxins and ciguatoxins Tetrahedron Letters. 39: 8321-8324. DOI: 10.1016/S0040-4039(98)01825-5 |
0.551 |
|
| 1998 |
Clark JS, Tolhurst KF, Taylor M, Swallow S. Enantioselective propargylic oxidation Tetrahedron Letters. 39: 4913-4916. DOI: 10.1016/S0040-4039(98)00894-6 |
0.383 |
|
| 1998 |
Clark JS, Fretwell M, Whitlock GA, Burns CJ, Fox DNA. Asymmetric synthesis of cyclic ethers by rearrangement of oxonium ylides generated from chiral copper carbenoids Tetrahedron Letters. 39: 97-100. DOI: 10.1016/S0040-4039(97)10441-5 |
0.463 |
|
| 1997 |
Burton JW, Clark JS, Derrer S, Stork TC, Bendall JG, Holmes AB. Synthesis of medium ring ethers. 5. The synthesis of (±)-laurencin Journal of the American Chemical Society. 119: 7483-7498. DOI: 10.1021/Ja9709132 |
0.672 |
|
| 1997 |
Clark JS, Kettle JG. Enantioselective synthesis of medium-ring sub-units of brevetoxin A by ring-closing metathesis Tetrahedron Letters. 38: 127-130. DOI: 10.1016/S0040-4039(96)02233-2 |
0.531 |
|
| 1997 |
Clark JS, Kettle JG. Synthesis of brevetoxin sub-units by sequential ring-closing metathesis and hydroboration Tetrahedron Letters. 38: 123-126. DOI: 10.1016/S0040-4039(96)02232-0 |
0.401 |
|
| 1996 |
JWBRA, Clark JS, Bendall J, Derrer S, Stork aT, Holmes AB. Synthesis of (+)-LaurencinA Retraction J. Am. Chem. Soc. 1993, 115, 10400−10401 Journal of the American Chemical Society. 118: 6806-6806. DOI: 10.1021/Ja965406J |
0.5 |
|
| 1996 |
Clark JS, Dossetter AG, Whittingham WG. Stereoselective synthesis of the bicyclic core structure of the highly oxidised sesquiterpene neoliacinic acid Tetrahedron Letters. 37: 5605-5608. DOI: 10.1016/0040-4039(96)01136-7 |
0.494 |
|
| 1995 |
Clark JS, Hodgson PB. An enantioselective synthesis of the CE ring system of the alkaloids manzamine A, E and F, and ircinal a Tetrahedron Letters. 36: 2519-2522. DOI: 10.1016/0040-4039(95)00296-O |
0.478 |
|
| 1994 |
Clark JS, Hodgson PB. Intramolecular generation and rearrangement of ammonium ylides from copper carbenoids: A general method for the synthesis of cyclic amines Journal of the Chemical Society, Chemical Communications. 2701-2702. DOI: 10.1039/C39940002701 |
0.447 |
|
| 1994 |
Clark JS, Whitlock GA. A short synthesis of (±)-decarestrictine L Tetrahedron Letters. 35: 6381-6382. DOI: 10.1016/S0040-4039(00)73438-1 |
0.396 |
|
| 1993 |
Robinson RA, Clark JS, Holmes AB. Synthesis of (+)-laurencin Journal of the American Chemical Society. 115: 10400-10401. DOI: 10.1021/Ja00075A082 |
0.604 |
|
| 1993 |
Clark JS, Krowiak SA, Street LJ. Synthesis of cyclic ethers from copper carbenoids by formation and rearrangement of oxonium ylides Tetrahedron Letters. 34: 4385-4388. DOI: 10.1016/S0040-4039(00)79359-2 |
0.501 |
|
| 1992 |
Carling RW, Clark JS, Holmes AB, Sartor D. Synthesis of medium ring ethers. Part 3. Disproof of the proposed 2,8-disubstituted oxocane structure for gloeosporone. Synthesis of pseudo-gloeosporone Journal of the Chemical Society-Perkin Transactions 1. 95-101. DOI: 10.1039/P19920000095 |
0.625 |
|
| 1992 |
Carling RW, Clark JS, Holmes AB. Synthesis of medium ring ethers. Part 2. Synthesis of the fully saturated carbon skeleton of Laurencia non-terpenoid ether metabolites containing seven-, eight- and nine-membered rings Journal of the Chemical Society-Perkin Transactions 1. 83-94. DOI: 10.1039/P19920000083 |
0.604 |
|
| 1992 |
Clark JS. Diastereoselective synthesis of 2,5-dialkyl tetrahydrofuran-3-ones by a copper-catalysed tandem carbenoid insertion and ylide rearrangement reaction Tetrahedron Letters. 33: 6193-6196. DOI: 10.1016/S0040-4039(00)60041-2 |
0.47 |
|
| 1992 |
Evans DA, Ng HP, Clark JS, Rieger DL. Diastereoselective Anti Aldol Reactions of Chiral Ethyl Ketones. Enantioselective Processes for the Synthesis of Polypropionate Natural Products. Tetrahedron. 48: 2127-2142. DOI: 10.1016/S0040-4020(01)88879-7 |
0.486 |
|
| 1990 |
Evans DA, Urpi F, Somers TC, Clark JS, Bilodeau MT. New procedure for the direct generation of titanium enolates. Diastereoselective bond constructions with representative electrophiles Journal of the American Chemical Society. 112: 8215-8216. DOI: 10.1021/Ja00178A082 |
0.317 |
|
| 1990 |
Evans DA, Clark JS, Metternich R, Novack VJ, Sheppard GS. Diastereoselective aldol reactions using .beta.-keto imide derived enolates. A versatile approach to the assemblage of polypropionate systems Journal of the American Chemical Society. 112: 866-868. DOI: 10.1021/Ja00158A056 |
0.37 |
|
| 1989 |
CLARK JS, HOLMES AB. ChemInform Abstract: A Strategy for the Asymmetric Synthesis of Medium Ring Oxygen Heterocycles: Enantioselective Total Synthesis of (+)-Octahydrodeacetyldebromolaurencin. Cheminform. 20. DOI: 10.1002/chin.198908212 |
0.575 |
|
| 1988 |
Clark JS, Holmes AB. A strategy for the asymmetric synthesis of medium ring oxygen heterocycles: Enantioselective total synthesis of (+)-octahydrodeacetyldebromolaurencin Tetrahedron Letters. 29: 4333-4336. DOI: 10.1016/S0040-4039(00)80490-6 |
0.638 |
|
| Show low-probability matches. |
