| Year |
Citation |
Score |
| 2019 |
Mears PR, Hoekman S, Rye CE, Bailey FP, Byrne DP, Eyers PA, Thomas EJ. Towards 20,20-difluorinated bryostatin: synthesis and biological evaluation of C17,C27-fragments. Organic & Biomolecular Chemistry. PMID 30681118 DOI: 10.1039/C8Ob03152E |
0.465 |
|
| 2019 |
Thomas EJ, Tray DR. 1,5-Stereocontrol in reactions of 2,4-disubstituted alk-2-enylstannanes with aldehydes; an approach to the stereoselective synthesis of branched triols Tetrahedron. 75: 130734. DOI: 10.1016/J.Tet.2019.130734 |
0.503 |
|
| 2018 |
Butler E, Florentino L, Cornut D, Gomez-Campillos G, Liu H, Regan AC, Thomas EJ. Synthesis of macrocyclic precursors of the vioprolides. Organic & Biomolecular Chemistry. PMID 30226509 DOI: 10.1039/C8Ob01756E |
0.438 |
|
| 2018 |
Burnell ES, Irshad A, Lee ATL, Thomas EJ. Synthetic approaches to phomactins: Late stage stereochemical and reactivity issues Tetrahedron. 74: 6737-6748. DOI: 10.1016/J.Tet.2018.10.004 |
0.432 |
|
| 2018 |
Blackburn TJ, Thomas EJ. Synthetic approaches to phomactins: Novel oxidation of homoallylic alcohols using tetra- n -propylammonium perruthenate Tetrahedron. 74: 5399-5407. DOI: 10.1016/J.Tet.2018.05.068 |
0.39 |
|
| 2017 |
Green AP, Hardy S, Lee ATL, Thomas EJ. Total synthesis of 7-des-O-pivaloyl-7-O-benzylbryostatin 10. Organic & Biomolecular Chemistry. PMID 29109995 DOI: 10.1039/C7Ob02129A |
0.464 |
|
| 2017 |
Green AP, Hardy S, Thomas EJ. Synthetic approaches to the C11-C27 fragments of bryostatins. Organic & Biomolecular Chemistry. PMID 29109991 DOI: 10.1039/C7Ob02127E |
0.427 |
|
| 2017 |
Dumeunier R, Gregson T, MacCormick S, Omori H, Thomas EJ. Some limitations of an approach to the assembly of bryostatins by ring-closing metathesis. Organic & Biomolecular Chemistry. PMID 28272610 DOI: 10.1039/C7Ob00079K |
0.445 |
|
| 2017 |
Ball M, Gregson T, Omori H, Thomas EJ. Syntheses of C17-C27 fragments of 20-deoxybryostatins for assembly using Julia and metathesis reactions. Organic & Biomolecular Chemistry. PMID 28271111 DOI: 10.1039/C7Ob00076F |
0.527 |
|
| 2017 |
Gregson T, Thomas EJ. Synthesis of vinylic iodides for incorporation into the C17-C27 fragment of bryostatins Tetrahedron. 73: 3316-3328. DOI: 10.1016/J.Tet.2017.04.048 |
0.447 |
|
| 2016 |
Ball M, Baron A, Bradshaw B, Dumeunier R, O'Brien M, Thomas EJ. The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins. Organic & Biomolecular Chemistry. PMID 27714213 DOI: 10.1039/C6Ob01804A |
0.585 |
|
| 2016 |
Broadley KJ, Burnell E, Davies RH, Lee AT, Snee S, Thomas EJ. The synthesis of a series of adenosine A3 receptor agonists. Organic & Biomolecular Chemistry. PMID 27001924 DOI: 10.1039/C6Ob00244G |
0.396 |
|
| 2016 |
Broadley KJ, Buffat MG, Burnell E, Davies RH, Moreau X, Snee S, Thomas EJ. Stereoselective synthesis of oxazolidinonyl-fused piperidines of interest as selective muscarinic (M1) receptor agonists: a novel M1 allosteric modulator. Organic & Biomolecular Chemistry. PMID 26768599 DOI: 10.1039/C5Ob02588E |
0.474 |
|
| 2016 |
Broadley KJ, Buffat MGP, Davies RH, Thomas EJ. A Stereoselective Synthesis of a 3,4,5-Substituted Piperidine of Interest as a Selective Muscarinic (M1) Receptor Agonist Synlett. 27: 45-50. DOI: 10.1055/S-0035-1560753 |
0.484 |
|
| 2016 |
Buffat MGP, Thomas EJ. Approaches to 3,4,5-substituted piperidines via 1,2,5,6-tetrahydropyridines prepared by ring-closing metathesis Tetrahedron. 72: 451-463. DOI: 10.1016/J.Tet.2015.11.040 |
0.433 |
|
| 2015 |
Mears PR, Thomas EJ. Difluoroallylation using a 2-bromomethyl-1,1-difluoroalk-1-ene Tetrahedron Letters. 56: 3980-3981. DOI: 10.1016/J.Tetlet.2015.05.009 |
0.473 |
|
| 2015 |
Mears PR, Thomas EJ. Synthesis of C16-C27-fragments of bryostatins modified by 20,20-difluorination Tetrahedron Letters. 56: 3975-3979. DOI: 10.1016/J.Tetlet.2015.05.007 |
0.466 |
|
| 2015 |
Hoather HA, Raftery J, Yalavac I, Thomas EJ. On the stereoselectivities of some hindered Diels-Alder reactions Tetrahedron. 71: 4124-4131. DOI: 10.1016/J.Tet.2015.04.101 |
0.47 |
|
| 2015 |
Blackburn TJ, Kilner MJ, Thomas EJ. Synthetic approaches to phomactins: On the stereoselectivity ofsome [2,3]-Wittig rearrangements Tetrahedron. DOI: 10.1016/J.Tet.2015.04.005 |
0.46 |
|
| 2014 |
Thomas EJ, Willis M. Approaches to the total synthesis of chaetochalasin A. Organic & Biomolecular Chemistry. 12: 7537-50. PMID 25119649 DOI: 10.1039/C4Ob01308E |
0.505 |
|
| 2014 |
Basar N, Damodaran K, Liu H, Morris GA, Sirat HM, Thomas EJ, Curran DP. Systematic comparison of sets of (13)C NMR spectra that are potentially identical. Confirmation of the configuration of a cuticular hydrocarbon from the cane beetle Antitrogus parvulus. The Journal of Organic Chemistry. 79: 7477-90. PMID 25019530 DOI: 10.1021/Jo5012027 |
0.338 |
|
| 2014 |
Basar N, Donelly S, Liu H, Thomas EJ. Erratum: 1,5-Stereocontrol in bismuth-mediated reactions between aldehydes and allyl bromides: Stereoselective synthesis of open-chain all- syn - And anti, anti -1,3,5-disposed trimethylalkanes (Synlett (2010) (575)) Synlett. 25. DOI: 10.1055/S-0033-1340184 |
0.444 |
|
| 2014 |
Burnell ES, Irshad AR, Raftery J, Thomas EJ. Approaches to phomactin A: Unexpected late-stage observations Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2015.01.082 |
0.377 |
|
| 2014 |
Thomas EJ, Weston AP. Open-chain remote stereocontrol using allylgermanes Tetrahedron. DOI: 10.1016/J.Tet.2014.06.053 |
0.473 |
|
| 2013 |
Basar N, Donnelly S, Sirat HM, Thomas EJ. Development and applications of remote stereocontrol using allylic organobismuth reagents. Organic & Biomolecular Chemistry. 11: 8476-505. PMID 24212203 DOI: 10.1039/C3Ob41931B |
0.487 |
|
| 2013 |
Liu H, Thomas EJ. Synthesis of the (E)-dehydrobutyrine-thiazoline-proline-leucine fragment of vioprolides B and D Tetrahedron Letters. 54: 3150-3153. DOI: 10.1016/J.Tetlet.2013.04.017 |
0.344 |
|
| 2013 |
Burns T, Helliwell M, Thomas EJ. An asymmetric synthesis of the pentacyclic core of stemofoline Tetrahedron Letters. 54: 2120-2123. DOI: 10.1016/J.Tetlet.2013.01.110 |
0.405 |
|
| 2012 |
Germay O, Kumar N, Moore CG, Thomas EJ. Total syntheses of pamamycin 607 and methyl nonactate: stereoselective cyclisation of homoallylic alcohols that had been prepared with remote stereocontrol using allylstannanes. Organic & Biomolecular Chemistry. 10: 9709-33. PMID 23154487 DOI: 10.1039/C2Ob26801A |
0.488 |
|
| 2012 |
Martin N, Thomas EJ. Total synthesis of epothilones using functionalised allylstannanes for remote stereocontrol. Organic & Biomolecular Chemistry. 10: 7952-64. PMID 22940725 DOI: 10.1039/C2Ob26310F |
0.47 |
|
| 2012 |
Hobson LA, Thomas EJ. Concerning the 1,5-stereocontrol in tin(IV) chloride promoted reactions of 4- and 5-alkoxyalk-2-enylstannanes: trapping intermediate allyltin trichlorides using phenyllithium. Organic & Biomolecular Chemistry. 10: 7510-26. PMID 22885896 DOI: 10.1039/C2Ob25765C |
0.463 |
|
| 2012 |
Hoegenauer EK, Thomas EJ. An approach to aliphatic 1,8-stereocontrol: diastereoselective syntheses of (±)-patulolide C and (±)-epipatulolide C. Organic & Biomolecular Chemistry. 10: 6995-7014. PMID 22832791 DOI: 10.1039/C2Ob25992C |
0.447 |
|
| 2012 |
Hallett DJ, Tanikkul N, Thomas EJ. Remote stereocontrol in reactions between 4- and 5-alkoxyalk-2-enylstannanes and 1-alkoxycarbonylimines and analogues: stereoselective approaches to novel α-amino acids. Organic & Biomolecular Chemistry. 10: 6130-58. PMID 22514049 DOI: 10.1039/C2Ob25097G |
0.498 |
|
| 2012 |
Basar NB, Liu H, Negi D, Sirat HM, Morris GA, Thomas EJ. Total synthesis of a cuticular hydrocarbon from the cane beetle Antitrogus parvulus: confirmation of the relative stereochemistry. Organic & Biomolecular Chemistry. 10: 1743-5. PMID 22274635 DOI: 10.1039/C2Ob06906G |
0.375 |
|
| 2012 |
Stanway SJ, Thomas EJ. 1,5-Stereocontrol in tin(IV) halide mediated reactions between N- and S-substituted pent-2-enylstannanes and aldehydes or imines Tetrahedron. 68: 5998-6009. DOI: 10.1016/J.Tet.2012.05.032 |
0.487 |
|
| 2011 |
Green AP, Lee AT, Thomas EJ. Total synthesis of a 20-deoxybryostatin. Chemical Communications (Cambridge, England). 47: 7200-2. PMID 21614401 DOI: 10.1039/C1Cc12332G |
0.42 |
|
| 2011 |
Carey JS, MacCormick S, Stanway SJ, Teerawutgulrag A, Thomas EJ. Effective 1,5-, 1,6- and 1,7-remote stereocontrol in reactions of alkoxy- and hydroxy-substituted allylstannanes with aldehydes. Organic & Biomolecular Chemistry. 9: 3896-919. PMID 21472165 DOI: 10.1039/C0Ob01084G |
0.508 |
|
| 2011 |
Broadley KJ, Davies RH, Escargueil C, Lee ATL, Penson P, Thomas EJ. Synthesis of antagonists of muscarinic (M3) receptors Collection of Czechoslovak Chemical Communications. 76: 781-801. DOI: 10.1135/Cccc2011017 |
0.356 |
|
| 2011 |
Thomas EJ, Tray DR. Stereochemical aspects of the chemistry of 2-[trialkyl(aryl)silyloxy]alkyl- 4-alkoxyalk-2-enylstannanes Tetrahedron Letters. 52: 2065-2068. DOI: 10.1016/J.Tetlet.2010.10.096 |
0.469 |
|
| 2011 |
O'Brien M, Thomas EJ. Synthesis of the C(1)-C(16) fragment of bryostatins using an 'ene' reaction between an allylsilane and an alkynone Tetrahedron. 67: 10068-10081. DOI: 10.1016/J.Tet.2011.09.064 |
0.535 |
|
| 2011 |
Gill D, Taylor NH, Thomas EJ. Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition Tetrahedron. 67: 5034-5045. DOI: 10.1016/J.Tet.2011.03.113 |
0.494 |
|
| 2011 |
McNeill AH, Thomas EJ. Applications of remote stereocontrol using allylstannanes: an approach to the stereoselective synthesis of aliphatic polyols Tetrahedron. 67: 257-266. DOI: 10.1016/J.Tet.2010.10.045 |
0.479 |
|
| 2010 |
Bazar N, Donnelly S, Liu H, Thomas EJ. 1,5-Stereocontrol in Bismuth-Mediated Reactions between Aldehydes and Allyl Bromides: Stereoselective Synthesis of Open-Chain all-syn- and anti, anti-1,3,5-Disposed Trimethylalkanes Synlett. 2010: 575-578. DOI: 10.1055/S-0029-1219357 |
0.432 |
|
| 2010 |
Brain CT, Chen A, Nelson A, Tanikkul N, Thomas EJ. Synthesis of macrocyclic precursors of lankacidins using Stille reactions of 4-(2-iodo-alkenyl)azetidinones and related compounds for ring closure Tetrahedron. 66: 6613-6625. DOI: 10.1016/J.Tet.2010.04.129 |
0.554 |
|
| 2010 |
Green AP, Hardy S, Lee ATL, Thomas EJ. Approaches to the total synthesis of biologically active natural products: Studies directed towards bryostatins Phytochemistry Reviews. 9: 501-513. DOI: 10.1007/S11101-010-9186-9 |
0.463 |
|
| 2010 |
Dortling EK, Thomas EJ. ChemInform Abstract: 1,8-Stereocontrol by 1,5-Induction Using an Allylstannane Followed by Ireland-Claisen Rearrangement: Diastereoselective Total Synthesis of (.+-.)-Patulolide C. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199917271 |
0.36 |
|
| 2010 |
Baxter J, Mata EG, Thomas EJ. ChemInform Abstract: An Approach to the Synthesis of the C(17)-C(27) Fragment of Bryostatins. Cheminform. 30: no-no. DOI: 10.1002/chin.199910255 |
0.607 |
|
| 2010 |
ALMENDROS P, THOMAS EJ. ChemInform Abstract: Stereoselectivity of Reactions of Alkoxyallylstannanes and Alkoxy Aldehydes. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199751062 |
0.351 |
|
| 2010 |
THOMAS EJ. ChemInform Abstract: Asymmetric Synthesis Using Main Group Allylmetal Reagents - Remote Asymmetric Induction Using Allylstannanes Cheminform. 27: no-no. DOI: 10.1002/chin.199651332 |
0.306 |
|
| 2010 |
MAGUIRE RJ, THOMAS EJ. ChemInform Abstract: 1,5-Asymmetric Induction in Reactions Between Aldehydes and ((4S)-5-( tert-Butyldimethylsilyloxy)-4-hydroxypent-2-enyl)(tributyl)stannane Promoted by Tin(IV) Chloride. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199605046 |
0.348 |
|
| 2010 |
TEERAWUTGULRAG A, THOMAS EJ. ChemInform Abstract: 1,5-Asymmetric Induction in Lewis Acid-Promoted Reactions of (5-Alkoxy- 2,4-dimethylpent-2-enyl)tributylstannanes and Aldehydes. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199410069 |
0.329 |
|
| 2010 |
CAREY JS, THOMAS EJ. ChemInform Abstract: 1,6-Asymmetric Induction in Lewis Acid-Promoted Reactions of .epsilon.- Methoxy- and .epsilon.-Hydroxyallylstannanes and Aldehydes. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199346058 |
0.331 |
|
| 2010 |
THOMAS EJ. ChemInform Abstract: Total Synthesis of Cytochalasans Cheminform. 24: no-no. DOI: 10.1002/CHIN.199339334 |
0.32 |
|
| 2010 |
THOMAS EJ. ChemInform Abstract: Cytochalasan Synthesis: Macrocycle Formation via Intramolecular Diels- Alder Reactions Cheminform. 22: no-no. DOI: 10.1002/CHIN.199150313 |
0.399 |
|
| 2009 |
McGowan G, Thomas EJ. Synthesis of macrocyclic precursors of phomactins using [2,3]-Wittig rearrangements. Organic & Biomolecular Chemistry. 7: 2576-90. PMID 19503933 DOI: 10.1039/B903256H |
0.442 |
|
| 2009 |
Blackburn TJ, Helliwell M, Kilner MJ, Lee ATL, Thomas EJ. Further studies of an approach to a total synthesis of phomactins Tetrahedron Letters. 50: 3550-3554. DOI: 10.1016/J.Tetlet.2009.03.042 |
0.502 |
|
| 2009 |
Thomas EJ, Vickers CF. An approach to an asymmetric synthesis of stemofoline Tetrahedron-Asymmetry. 20: 970-979. DOI: 10.1016/J.Tetasy.2009.03.002 |
0.377 |
|
| 2009 |
Shapland PDP, Thomas EJ. Synthesis of precursors of phomactins using [2,3]-Wittig rearrangements Tetrahedron. 65: 4201-4211. DOI: 10.1016/J.Tet.2009.03.031 |
0.505 |
|
| 2008 |
Evans P, Lee AT, Thomas EJ. Synthesis of a 6-aryloxymethyl-5-hydroxy-2,3,4,5-tetrahydro-[1H]-2-benzazepin-4-one: a muscarinic (M3) antagonist. Organic & Biomolecular Chemistry. 6: 2158-67. PMID 18528577 DOI: 10.1039/B801208C |
0.424 |
|
| 2008 |
Bradshaw B, Evans P, Fletcher J, Lee AT, Mwashimba PG, Oehlrich D, Thomas EJ, Davies RH, Allen BC, Broadley KJ, Hamrouni A, Escargueil C. Synthesis of 5-hydroxy-2,3,4,5-tetrahydro-[1H]-2-benzazepin-4-ones: selective antagonists of muscarinic (M3) receptors. Organic & Biomolecular Chemistry. 6: 2138-57. PMID 18528576 DOI: 10.1039/B801206G |
0.348 |
|
| 2008 |
Green AP, Hardy S, Thomas EJ. A synthesis of the C(17)-C(27) fragment of bryostatin 1 Synlett. 2103-2106. DOI: 10.1055/S-2008-1078015 |
0.373 |
|
| 2008 |
Allen JV, Green AP, Hardy S, Heron NM, Lee ATL, Thomas EJ. On the use of the modified Julia olefination for bryostatin synthesis Tetrahedron Letters. 49: 6352-6355. DOI: 10.1016/J.Tetlet.2008.08.075 |
0.441 |
|
| 2007 |
Baylis AM, Davies MP, Thomas EJ. Synthetic approaches to the polycyclic alkaloid stemofoline. Organic & Biomolecular Chemistry. 5: 3139-55. PMID 17878973 DOI: 10.1039/B708910D |
0.483 |
|
| 2007 |
Thomas EJ. Remote stereocontrol using functionalized allylmetal reagents. Chemical Record (New York, N.Y.). 7: 115-24. PMID 17394173 DOI: 10.1002/Tcr.20113 |
0.457 |
|
| 2007 |
Thomas EJ, Weston AP. 1,6-Remote stereocontrol using allylgermanes Tetrahedron Letters. 48: 341-343. DOI: 10.1016/J.Tetlet.2006.11.070 |
0.365 |
|
| 2007 |
Castreno P, Thomas EJ, Weston AP. 1,5-Remote stereocontrol using allylgermanes Tetrahedron Letters. 48: 337-340. DOI: 10.1016/J.Tetlet.2006.11.065 |
0.357 |
|
| 2007 |
Baylis AM, Thomas EJ. Aspects of the chemistry of 8-azabicyclo[3.2.1]octanes Tetrahedron. 63: 11666-11671. DOI: 10.1016/J.Tet.2007.08.109 |
0.492 |
|
| 2007 |
Kumar P, Thomas EJ, Tray D. 1,5-Stereocontrol in tin(IV) halide promoted reactions of 2-alkoxy-1-(2-tributylstannylethylidene)cyclohexanes with aldehydes Tetrahedron. 63: 6287-6295. DOI: 10.1016/J.Tet.2007.03.070 |
0.388 |
|
| 2006 |
Helliwell M, Thomas EJ, Vickers C. An observation on the regioselectivity of ring-opening of some substituted cyclohexenyl epoxides Arkivoc. 2007. DOI: 10.3998/Ark.5550190.0008.717 |
0.416 |
|
| 2006 |
Booth M, Brain C, Castreno P, Donnelly S, Dorling EK, Germay O, Hobson L, Kumar N, Martin N, Moore C, Negi D, Thomas EJ, Weston A. Alternatives to allylstannanes for remote stereocontrol Pure and Applied Chemistry. 78: 2015-2028. DOI: 10.1351/Pac200678112015 |
0.437 |
|
| 2006 |
Ball M, Bradshaw BJ, Dumeunier R, Gregson TJ, MacCormick S, Omori H, Thomas EJ. A preliminary evaluation of a metathesis approach to bryostatins Tetrahedron Letters. 47: 2223-2227. DOI: 10.1016/J.Tetlet.2006.01.097 |
0.45 |
|
| 2006 |
MacCormick S, Thomas EJ. Remote stereocontrol using (E)-6-hydroxy-4-methylhex-2-enyl(tri-n-butyl) stannane Journal of Organometallic Chemistry. 691: 1437-1440. DOI: 10.1002/CHIN.200632039 |
0.432 |
|
| 2005 |
Bailey S, Helliwell M, Teerawutgulrag A, Thomas EJ. A total synthesis of milbemycin G: approaches to the C1-C10-fragment and completion of the synthesis. Organic & Biomolecular Chemistry. 3: 3654-77. PMID 16211101 DOI: 10.1039/B508675B |
0.477 |
|
| 2005 |
Helliwell M, Karim S, Parmee ER, Thomas EJ. Total synthesis of milbemycins: a synthesis of (6R)-6-hydroxy-3,4-dihydromilbemycin E. Organic & Biomolecular Chemistry. 3: 3636-53. PMID 16211100 DOI: 10.1039/B508670A |
0.562 |
|
| 2005 |
Baron A, Ball M, Bradshaw B, Donnelly S, Germay O, Oller PC, Kumar N, Martin N, O’Brien M, Omori H, Moore C, Thomas EJ. Approaches to the stereoselective total synthesis of biologically active natural products Pure and Applied Chemistry. 77: 103-117. DOI: 10.1351/Pac200577010103 |
0.448 |
|
| 2005 |
Helliwell M, Thomas EJ, Whitehouse DL. A Diels-Alder approach to potential precursors of polyhydroxylated dihydroagarofurans: A ring-opening/ring-closing rearrangement Synthesis. 3235-3238. DOI: 10.1055/S-2005-918464 |
0.435 |
|
| 2004 |
Ball M, Baron A, Bradshaw B, Omori H, MacCormick S, Thomas EJ. A stereoselective synthesis of the C(1)–C(16) fragment of the bryostatins Tetrahedron Letters. 45: 8737-8740. DOI: 10.1016/J.Tetlet.2004.09.124 |
0.514 |
|
| 2004 |
Donnelly S, Thomas EJ, Fielding M. 1,5-Stereocontrol in reactions of 5-benzyloxy-4-methylpent-2-enyl bromides with aldehydes mediated by Bi(0): synthesis of aliphatic compounds with 1,5-syn-related methyl groups Tetrahedron Letters. 45: 6779-6782. DOI: 10.1016/J.Tetlet.2004.07.035 |
0.466 |
|
| 2003 |
Donnelly S, Thomas EJ, Arnott EA. Remote stereocontrol using allylstannanes: reversal in stereoselectivity using indium(III) and bismuth(III) halides as promoters. Chemical Communications (Cambridge, England). 1460-1. PMID 12841291 DOI: 10.1039/B303151A |
0.352 |
|
| 2003 |
Marsden A, Thomas EJ. An approach to the synthesis of phomactins using a Wittig rearrangement Arkivoc. 2002. DOI: 10.3998/Ark.5550190.0003.909 |
0.457 |
|
| 2003 |
Balnaves AS, McGowan G, Shapland PDP, Thomas EJ. Corrigendum to “Approaches to the total synthesis of phomactins” Tetrahedron Letters. 44: 4301. DOI: 10.1016/S0040-4039(03)00880-3 |
0.418 |
|
| 2003 |
Balnaves AS, McGowan G, Shapland PDP, Thomas EJ. Approaches to the total synthesis of phomactins Tetrahedron Letters. 44: 2713-2716. DOI: 10.1016/S0040-4039(03)00341-1 |
0.465 |
|
| 2002 |
Bailey S, Karim S, Thomas EJ. Total Synthesis of 3,4-Dihydromilbemycin G: Synthesis of the 'Lower Hemisphere' of α-Milbemycins and Avermectins Synlett. 1992: 840-842. DOI: 10.1055/S-1992-21512 |
0.379 |
|
| 2002 |
Helliwell M, Thomas EJ, Townsend LA. Synthesis of chiral organotin reagents: synthesis of enantiomerically enriched bicyclo[2.2.1]hept-2-yl tin hydrides from camphor. X-Ray crystal structures of (dimethyl)[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]tin chloride and methyl(phenyl)bis[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]stannane Journal of the Chemical Society-Perkin Transactions 1. 1286-1296. DOI: 10.1039/B200317C |
0.459 |
|
| 2002 |
O'Brien M, Taylor NH, Thomas EJ. Synthesis of the C(1)-C(16) fragment of bryostatins Tetrahedron Letters. 43: 5491-5494. DOI: 10.1016/S0040-4039(02)01054-7 |
0.431 |
|
| 2001 |
Hobson LA, Singh LW, Thomas EJ. Stereocontrolled syntheses of 2,5-disubstituted tetrahydrofurans using remote asymmetric induction Arkivoc. 2001. DOI: 10.3998/Ark.5550190.0002.807 |
0.494 |
|
| 2001 |
Kumar P, Thomas EJ, Tray DR. 1,5-Induction in reactions between 2-alkoxy-(2-tributylstannylethylidene)cyclohexanes and aldehydes Journal of the Brazilian Chemical Society. 12: 623-626. DOI: 10.1590/S0103-50532001000500005 |
0.406 |
|
| 2001 |
Martin N, Thomas EJ. Total syntheses of epothilones B and D: Applications of allylstannanes in organic synthesis Tetrahedron Letters. 42: 8373-8377. DOI: 10.1016/S0040-4039(01)01795-6 |
0.423 |
|
| 2001 |
Germay O, Kumar N, Thomas EJ. Total synthesis of pamamycin 607: applications of remote asymmetric induction in organic synthesis Tetrahedron Letters. 42: 4969-4974. DOI: 10.1016/S0040-4039(01)00921-2 |
0.536 |
|
| 2001 |
Chen A, Nelson A, Tanikkul N, Thomas EJ. An approach to the total synthesis of lankacidins: synthesis of advanced macrocyclic precursors Tetrahedron Letters. 42: 1251-1254. DOI: 10.1016/S0040-4039(00)02261-9 |
0.537 |
|
| 2001 |
Brain CT, Chen A, Nelson A, Tanikkul N, Thomas EJ. An approach to the total synthesis of lankacidins: synthesis of the requisite building blocks Tetrahedron Letters. 42: 1247-1250. DOI: 10.1016/S0040-4039(00)02260-7 |
0.537 |
|
| 2001 |
Deka DC, Helliwell M, Thomas EJ. Synthesis of chiral organotin reagents: synthesis and X-ray crystal structures of bicyclo[2.2.1]heptan-2-yl(diphenyl)tin chlorides with cis-disposed nitrogen containing substituents Tetrahedron. 57: 10017-10026. DOI: 10.1016/S0040-4020(01)01035-3 |
0.456 |
|
| 2000 |
Almendros P, Rae A, Thomas EJ. Synthesis of the C(17)-C(27) fragment of the 20-deoxybryostatins Tetrahedron Letters. 41: 9565-9568. DOI: 10.1016/S0040-4039(00)01697-X |
0.441 |
|
| 1999 |
Vincent MA, Hillier IH, Hall RJ, Thomas EJ. Stereospecificity in Reactions of Allylstannanes with Aldehydes Explored by Electronic Structure Calculations. The Journal of Organic Chemistry. 64: 4680-4684. PMID 11674539 DOI: 10.1021/Jo9824551 |
0.375 |
|
| 1999 |
Thomas EJ, Watts JP. Synthesis of cytochalasans using intramolecular Diels–Alder reactions: an alternative approach to cytochalasin D Journal of the Chemical Society-Perkin Transactions 1. 3285-3290. DOI: 10.1039/A906414A |
0.502 |
|
| 1999 |
Merifield E, Thomas EJ. Total synthesis of cytochalasin D: total synthesis and full structural assignment of cytochalasin O Journal of the Chemical Society-Perkin Transactions 1. 3269-3283. DOI: 10.1039/A906412E |
0.505 |
|
| 1999 |
Savage I, Thomas EJ, Wilson PD. Stereoselective synthesis of allylic amines by rearrangement of allylic trifluoroacetimidates: stereoselective synthesis of polyoxamic acid and derivatives of other α-amino acids Journal of the Chemical Society-Perkin Transactions 1. 3291-3303. DOI: 10.1039/A905772B |
0.462 |
|
| 1999 |
Chen A, Thomas EJ, Wilson PD. Stereoselective synthesis of thymine polyoxin C using an allylic trifluoroacetimidate–trifluoroacetamide rearrangement Journal of the Chemical Society-Perkin Transactions 1. 3305-3310. DOI: 10.1039/A905771D |
0.49 |
|
| 1999 |
Broady SD, Rexhausen JE, Thomas EJ. Total synthesis of AI-77-B: stereoselective hydroxylation of 4-alkenylazetidinones Journal of the Chemical Society-Perkin Transactions 1. 1083-1094. DOI: 10.1039/A900334G |
0.436 |
|
| 1999 |
Dorling EK, Thomas AP, Thomas EJ. 1,8-Stereocontrol by 1,5-induction using an allylstannane followed by a 2,3-Wittig rearrangement: Diastereoselective total synthesis of (±)- epipatulolide C Tetrahedron Letters. 40: 475-476. DOI: 10.1016/S0040-4039(98)02428-9 |
0.447 |
|
| 1999 |
Dorling EK, Thomas EJ. 1,8-Stereocontrol by 1,5-induction using an allylstannane followed by Ireland-Claisen rearrangement: Diastereoselective total synthesis of (±)- patulolide C Tetrahedron Letters. 40: 471-474. DOI: 10.1016/S0040-4039(98)02427-7 |
0.446 |
|
| 1999 |
Taylor NH, Thomas EJ. 1,5-Induction in reactions of 4-alkoxy-2-trimethylsilylalk-2- enyl(tributyl)stannanes with aldehydes Tetrahedron. 55: 8757-8768. DOI: 10.1016/S0040-4020(99)00442-1 |
0.467 |
|
| 1999 |
Moffatt EM, Thomas EJ. 1,9-Stereocontrol from 1,7-induction using an allylstannane followed by an Ireland-Claisen rearrangement Tetrahedron. 55: 3723-3734. DOI: 10.1016/S0040-4020(98)01179-X |
0.377 |
|
| 1998 |
Smith PM, Thomas EJ. Approaches to a synthesis of galbonolide B Journal of the Chemical Society-Perkin Transactions 1. 3541-3556. DOI: 10.1039/A805856C |
0.491 |
|
| 1998 |
Gracia J, Thomas EJ. An approach to the C(17)–C(24) fragment of bryostatins: applications of stereoselective trisubstituted alkene formation by palladium(0) catalysed coupling of enol acetates and vinylic bromides Journal of the Chemical Society-Perkin Transactions 1. 2865-2872. DOI: 10.1039/A803425G |
0.463 |
|
| 1998 |
Maguire RJ, Munt SP, Thomas EJ. An approach to the C(10)–C(16) fragment of the bryostatins: stereoselective exocyclic double-bond formation by vinyl radical cyclization Journal of the Chemical Society-Perkin Transactions 1. 2853-2864. DOI: 10.1039/A803422B |
0.46 |
|
| 1998 |
Hobson LA, Vincent MA, Thomas EJ. On the origin of 1,5-induction in tin(IV) halide-promoted reactions of 4-alkoxyalk-2-enylstannanes with aldehydes Chemical Communications. 899-900. DOI: 10.1039/A800781K |
0.41 |
|
| 1998 |
Mellor BJ, Thomas EJ. Synthesis of analogues of oligonucleotides; synthesis of unprotected C-linked di- and tri-nucleotides Journal of the Chemical Society-Perkin Transactions 1. 747-758. DOI: 10.1039/A706858A |
0.443 |
|
| 1998 |
Butterfield K, Thomas EJ. Synthesis of analogues of nucleotides with all-carbon backbones: synthesis of N-protected C-linked dinucleotides Journal of the Chemical Society-Perkin Transactions 1. 737-746. DOI: 10.1039/A706857C |
0.456 |
|
| 1998 |
Pratt RM, Thomas EJ. Synthesis of chiral organotin reagents: synthesis of bicyclo[2.2.1]heptan-2-yl(diphenyl)tin hydrides with cis-disposed, oxygen-containing substituents Journal of the Chemical Society-Perkin Transactions 1. 727-736. DOI: 10.1039/A706295H |
0.481 |
|
| 1998 |
Beddoes R, Pratt RM, Thomas EJ. Synthesis of chiral organotin reagents: synthesis of diphenyl- {(1S,2R,3S,4R)-3-(alkoxymethyl)bicyclo[2.2.1]heptan-2-yl}tin hydrides. X-Ray crystal structure of (R)-4,4-dimethyl-2-oxotetrahydrofuran-3-yl (1S,2S,3R,4R)-3-triphenylstannylbicyclo[2.2.1]hept-5-ene-2-carboxylate Journal of the Chemical Society-Perkin Transactions 1. 717-726. DOI: 10.1039/A706293A |
0.387 |
|
| 1998 |
McNeill AH, Mortlock SV, Pratt RM, Thomas EJ. Synthesis of chiral organotin reagents: Diels–Alder reactions of methyl 3-(triphenylstannyl)acrylate: synthesis of diphenyl(3-substituted bicyclo[2.2.1]heptan-2-yl)tin hydrides Journal of the Chemical Society-Perkin Transactions 1. 709-716. DOI: 10.1039/A706291E |
0.515 |
|
| 1998 |
Baxter J, Mata EG, Thomas EJ. An approach to the synthesis of the C(17)-C(27) fragment of bryostatins Tetrahedron. 54: 14359-14376. DOI: 10.1016/S0040-4020(98)00889-8 |
0.657 |
|
| 1998 |
Mortlock SV, Thomas EJ. Aspects of the chemistry of 4-tributylstannyl-, 4-trimethylsilyl- and 2- phenylsulfinylallylstannanes Tetrahedron. 54: 4663-4672. DOI: 10.1016/S0040-4020(98)00183-5 |
0.453 |
|
| 1998 |
Mellor BJ, Murray PE, Thomas EJ. Aspects of the chemistry of dioxolanes: Synthesis of C-nucleoside analogues Tetrahedron. 54: 243-256. DOI: 10.1016/S0040-4020(97)10274-5 |
0.477 |
|
| 1997 |
Bradley GW, Thomas EJ. Stereoselective Synthesis of 2-(1-Alkoxyalkyl)-3-hydroxy-5-substituted-tetrahydrofurans Synlett. 1997: 629-631. DOI: 10.1055/S-1997-3220 |
0.503 |
|
| 1997 |
Arista L, Gruttadauria M, Thomas EJ. Stereoselective Synthesis of cis-2,5-Disubstituted Tetrahydrofurans: An Approach to Pamamycins Synlett. 1997: 627-628. DOI: 10.1055/S-1997-3219 |
0.374 |
|
| 1997 |
Almendros P, Thomas EJ. On The Stereoselectivity Of Reactions Of Alkoxyallylstannanes And Alkoxy Aldehydes Journal of the Chemical Society-Perkin Transactions 1. 2561-2568. DOI: 10.1039/A702257C |
0.43 |
|
| 1997 |
Almendros P, Gruttadauria M, Helliwell M, Thomas EJ. Stereoselective synthesis of 4-alkoxy-3-methylidenealkanols usingreactions between 2-(1-alkoxyalkyl)propenylstannanes and aldehydes:X-ray crystal structure of(1R,4R)-3-methylidene-1-(4-nitrophenyl)pentane-1,4-diol Journal of the Chemical Society-Perkin Transactions 1. 2549-2560. DOI: 10.1039/A702256E |
0.459 |
|
| 1997 |
Astles PC, Thomas EJ. Syntheses of thunbergols and α- and β-cembra-2,7,11-triene-4,6-diols Journal of the Chemical Society-Perkin Transactions 1. 845-856. DOI: 10.1039/A606551A |
0.526 |
|
| 1997 |
Steel PG, Parmee ER, Thomas EJ. Total synthesis of milbemycin E: resolution of the C(1)–C(10)fragment and final assembly Journal of the Chemical Society-Perkin Transactions 1. 391-400. DOI: 10.1039/A605894I |
0.666 |
|
| 1997 |
Parmee ER, Mortlock SV, Stacey NA, Thomas EJ. Total synthesis of milbemycin E: development of a procedure for the introduction of the 3,4-double bond and synthesis of the C(1)–C(10) fragment Journal of the Chemical Society-Perkin Transactions 1. 381-390. DOI: 10.1039/A605893K |
0.48 |
|
| 1997 |
Steel PG, Thomas EJ. Total synthesis of milbemycin E: synthesis of the C(11)–C(25)fragment Journal of the Chemical Society-Perkin Transactions 1. 371-380. DOI: 10.1039/A605892B |
0.694 |
|
| 1997 |
Chambers MS, Thomas EJ. Asymmetric synthesis of 5,5-disubstituted thiotetronic acids using anallyl xanthate to dithiocarbonate rearrangement: total synthesis of(5S)-thiolactomycin with revision of the absolute configurationof the natural Journal of the Chemical Society-Perkin Transactions 1. 417-432. DOI: 10.1039/A605768C |
0.432 |
|
| 1997 |
Thomas EJ. Control And Applications Of Remote Asymmetric Induction Using Allylmetal Reagents Chemical Communications. 411-418. DOI: 10.1039/A603881F |
0.434 |
|
| 1997 |
Brain CT, Thomas EJ. Remote asymmetric induction in reactions of 5-alkoxyalk-2-enylsilanes and aldehydes promoted by tin(IV) chloride Tetrahedron Letters. 38: 2387-2390. DOI: 10.1016/S0040-4039(97)00358-4 |
0.445 |
|
| 1997 |
Menager E, Merifield E, Smallridge M, Thomas EJ. A convergent synthesis of the C(11)–C(25) fragment of the aglycone of avermectin A2b Tetrahedron. 53: 9377-9392. DOI: 10.1016/S0040-4020(97)00590-5 |
0.478 |
|
| 1996 |
Carey JS, Coulter TS, Hallett DJ, Maguire RJ, McNeill AH, Stanway SJ, Teerawutgulrag A, Thomas EJ. Aspects of remote asymmetric induction using allylstannanes Pure and Applied Chemistry. 68: 707-710. DOI: 10.1351/Pac199668030707 |
0.396 |
|
| 1995 |
Stanway SJ, Thomas EJ. 1,5-Induction in Reactions between (5-Benzylthiopent-2-enyl)stannanes and Aldehydes promoted by Lewis Acids Synlett. 1995: 214-216. DOI: 10.1055/S-1995-4894 |
0.404 |
|
| 1995 |
Maguire RJ, Thomas EJ. Stereoselective synthesis of cis- and trans-2,6-disubstituted 5,6- dihydro-2H-pyrans based on 1,5-asymmetric induction in reactions between allylstannanes and aldehydes promoted by tin(IV) chloride Journal of the Chemical Society, Perkin Transactions 1. 2487-2495. DOI: 10.1039/P19950002487 |
0.437 |
|
| 1995 |
Maguire RJ, Thomas EJ. 1,5-Asymmetric induction in reactions between aldehydes and [(4S)-5-(tert-butyldimethylsilyloxy)-4-hydroxypent-2-enyl](tributyl)-stannane promoted by tin(IV) chloride Journal of the Chemical Society-Perkin Transactions 1. 2477-2485. DOI: 10.1039/P19950002477 |
0.5 |
|
| 1995 |
Gruttadauria M, Thomas EJ. 1,4-Asymmetric induction in reactions between [2-(1-alkoxyalkyl)propenyl](tributyl)stannanes and aldehydes promoted by tin(IV) halides Journal of the Chemical Society-Perkin Transactions 1. 1469-1471. DOI: 10.1039/P19950001469 |
0.458 |
|
| 1995 |
Mata EG, Thomas EJ. Development of a synthesis of lankacidins: an investigation into 17-membered ring formation Journal of the Chemical Society-Perkin Transactions 1. 785-799. DOI: 10.1039/P19950000785 |
0.729 |
|
| 1995 |
Roe JM, Thomas EJ. Development of a synthesis of lankacidins: synthesis of the C(14)–C(6) fragment and introduction of the C(10)–C(13) diene Journal of the Chemical Society-Perkin Transactions 1. 359-368. DOI: 10.1039/P19950000359 |
0.525 |
|
| 1995 |
Thomas EJ, Williams AC. Development of a synthesis of lankacidins: stereoselective synthesis of the δ-lactone fragment Journal of the Chemical Society-Perkin Transactions 1. 351-358. DOI: 10.1039/P19950000351 |
0.469 |
|
| 1995 |
Bailey S, Teerawutgulrag A, Thomas EJ. Total synthesis of milbemycin G: assembly and completion of the synthesis Journal of the Chemical Society, Chemical Communications. 2521-2522. DOI: 10.1039/C39950002521 |
0.423 |
|
| 1995 |
Bailey S, Teerawutgulrag A, Thomas EJ. Total synthesis of milbemycin G: Synthesis of the C(1)-C(10) fragment Journal of the Chemical Society, Chemical Communications. 2519-2520. DOI: 10.1039/C39950002519 |
0.396 |
|
| 1995 |
Hallett DJ, Thomas EJ. Remote asymmetric induction in reactions between 4- and 5-benzyloxypent-2-enyl(tributyl)stannanes and chiral imines prepared from butyl glyoxylate Journal of the Chemical Society, Chemical Communications. 657-658. DOI: 10.1039/C39950000657 |
0.486 |
|
| 1995 |
Bradley GW, Hallett DJ, Thomas EJ. The Effect of a tert-butyldimethylsilyl substituent on the 1,5-asymmetric induction found in reactions of 4- and 5-alkoxyallylstannanes with aldehydes and imines Tetrahedron-Asymmetry. 6: 2579-2582. DOI: 10.1016/0957-4166(95)00338-P |
0.446 |
|
| 1995 |
Hallett DJ, Thomas EJ. 1,5-Asymmetric induction in reactions between 4- and 5-alkoxypent-2-enyl(tributyl)stannanes and achiral 1-alkoxycarbonylimines Tetrahedron: Asymmetry. 6: 2575-2578. DOI: 10.1016/0957-4166(95)00337-O |
0.435 |
|
| 1995 |
Stanway SJ, Thomas EJ. 1,6-Asymmetric induction in reactions between 6-hydroxy-5-methylhex-2-enyl(tributyl)stannane and aldehydes promoted by tin(IV) bromide Tetrahedron Letters. 36: 3417-3420. DOI: 10.1016/0040-4039(95)00496-Y |
0.499 |
|
| 1994 |
Mcneill AH, Thomas EJ. Effective 1,5-asymmetric induction in tin(IV) chloride promoted reactions between aldehydes and (4-alkoxy-2-alkenyl)tributylstannanes Synthesis. 1994: 322-334. DOI: 10.1055/S-1994-25469 |
0.495 |
|
| 1994 |
Hallett DJ, Thomas EJ. Chelation controlled reactions between hydroxy- and alkoxy-ketones and prop-2-enyltin trihalides Synlett. 1994: 87-88. DOI: 10.1055/S-1994-22749 |
0.406 |
|
| 1994 |
Stanway SJ, Thomas EJ. 1,5-Induction in reactions between 4-aminoallylstannanes and aldehydes promoted by Lewis acids Journal of the Chemical Society, Chemical Communications. 285-286. DOI: 10.1039/C39940000285 |
0.458 |
|
| 1994 |
Carey JS, Thomas EJ. Effective 1,7-asymmetric induction in reactions between 6-hydroxyallylstannanes and aldehydes promoted by tin(IV) bromide Journal of the Chemical Society, Chemical Communications. 283-284. DOI: 10.1039/C39940000283 |
0.469 |
|
| 1993 |
Butterfield K, Thomas EJ. Synthesis of a Dinucleotide Analogue with an All-Carbon Backbone Synlett. 1993: 411-412. DOI: 10.1055/S-1993-22475 |
0.329 |
|
| 1993 |
Teerawutgulrag A, Thomas EJ. 1,5-Asymmetric induction in Lewis acid-promoted reactions of (5-alkoxy-2,4-dimethylpent-2-enyl)tributylstannanes and aldehydes Journal of the Chemical Society-Perkin Transactions 1. 2863-2864. DOI: 10.1039/P19930002863 |
0.46 |
|
| 1993 |
Khandekar G, Robinson GC, Stacey NA, Thomas EJ, Vather S. Milbemycin synthesis: asymmetric synthesis of spiroketals from methyl α-D-glucopyranoside Journal of the Chemical Society-Perkin Transactions 1. 1507-1519. DOI: 10.1039/P19930001507 |
0.538 |
|
| 1993 |
Hughes MJ, Thomas EJ. Milbemycin synthesis: synthesis of a macrocyclic analogue of non-aromatic β-milbemycins Journal of the Chemical Society-Perkin Transactions 1. 1493-1505. DOI: 10.1039/P19930001493 |
0.483 |
|
| 1993 |
Baylis AM, Helliwell M, Regan AC, Thomas EJ. Synthesis of 5-hydroxy-1,7-dioxaspiro[5.5]undec-3-en-2-ones from 2-benzenesulfonyltetrahydropyrans and 5-hydroxybutenolides: X-ray crystal structure determination for (5RS,6SR)-5-acetoxy-4-methoxy3-methyl-1,7-dioxaspiro[5.5]undec-3-en-2-one Journal of the Chemical Society-Perkin Transactions 1. 411-416. DOI: 10.1039/P19930000411 |
0.414 |
|
| 1993 |
Carey JS, Thomas EJ. 1,6-asymmetric induction in Lewis acid promoted reactions of ε-methoxy- and ε-hydroxy-allylstannanes and aldehydes Tetrahedron Letters. 34: 3935-3938. DOI: 10.1016/S0040-4039(00)79268-9 |
0.485 |
|
| 1993 |
Carey JS, Coulter TS, Thomas EJ. 15-asymmetric induction in reactions between (alkoxyallyl)stannanes and aldehydes: Influence of the Lewis acid and O-substituent Tetrahedron Letters. 34: 3933-3934. DOI: 10.1016/S0040-4039(00)79267-7 |
0.382 |
|
| 1993 |
Chen A, Savage I, Thomas EJ, Wilson PD. Asymmetric α-aminoacid synthesis using [3.3] rearrangement of allylic trifluoroacetimidates: Synthesis of thymine polyoxin C Tetrahedron Letters. 34: 6769-6772. DOI: 10.1016/S0040-4039(00)61697-0 |
0.479 |
|
| 1993 |
McNeill AH, Thomas EJ. Stereoselective synthesis of aliphatic 1,5,9,13-polyols using (δ-alkoxyallyl)stannanes Tetrahedron Letters. 34: 1669-1672. DOI: 10.1016/0040-4039(93)85037-W |
0.417 |
|
| 1992 |
Carey JS, Thomas EJ. Remote Asymmetric Induction in Reactions between Allylstannanes and Aldehydes: Influence of a Homoallyl Ether Substituent in the Stannane Synlett. 1992: 585-586. DOI: 10.1055/S-1992-21424 |
0.462 |
|
| 1992 |
Briggs MSJ, Helliwell M, Moorcroft D, Thomas EJ. Synthesis of thiospiroacetals. X-Ray crystal structure determinations for (7RS,11RS)-1,4,8-trioxa-13-thiadispiro[4.1.5.3]pentadecan-11-ol and (4RS,6SR)-4-p-nitrobenzoyloxy-1,7-dithiaspiro[5.5]undecane Journal of the Chemical Society-Perkin Transactions 1. 2223-2234. DOI: 10.1039/P19920002223 |
0.365 |
|
| 1992 |
Beddoes RL, Davies MPH, Thomas EJ. Synthesis of the tricyclic nucleus of the alkaloid stemofoline: X-ray crystal structure of (4RS,5RS,7SR,10RS)-10-butyl-5-hydroxy-1-azatricyclo[5.3.0.0]decan-2-one Journal of the Chemical Society, Chemical Communications. 538-540. DOI: 10.1039/C39920000538 |
0.387 |
|
| 1992 |
McNeill AH, Thomas EJ. 1,5-Asymmetric induction in reactions of δ-alkoxyallylstannanes: stereoselective reactions with chiral aldehydes Tetrahedron Letters. 33: 1369-1372. DOI: 10.1016/S0040-4039(00)91625-3 |
0.471 |
|
| 1991 |
Jephcote VJ, Thomas EJ. Synthesis of α-substituted allyl- and homoallyl-stannanes by selenoxide elimination Journal of the Chemical Society-Perkin Transactions 1. 429-434. DOI: 10.1039/P19910000429 |
0.373 |
|
| 1991 |
Broady SD, Rexhausen JE, Thomas EJ. Total synthesis of AI-77-B Journal of the Chemical Society, Chemical Communications. 708-710. DOI: 10.1039/C39910000708 |
0.385 |
|
| 1991 |
Thomas EJ. Cytochalasan synthesis: macrocycle formation via intramolecular Diels-Alder reactions Accounts of Chemical Research. 24: 229-235. DOI: 10.1021/AR00008A002 |
0.386 |
|
| 1991 |
Karim S, Parmee ER, Thomas EJ. Milbemycin synthesis: synthesis of 6β-hydroxy-3,4-dihydromilbemycin E Tetrahedron Letters. 32: 2269-2272. DOI: 10.1016/S0040-4039(00)79699-7 |
0.398 |
|
| 1990 |
Roe JM, Thomas EJ. Lankacidin Synthesis: Synthesis of the Lactone Fragment and an Improved Procedure for Stereoselective Acylation of a Chiral β-Lactam Synlett. 1990: 727-728. DOI: 10.1055/S-1990-21226 |
0.427 |
|
| 1990 |
McNeill AH, Thomas EJ. 1,5-Asymmetric induction in reactions betweenδ-alkoxyallylstannanes and aldehydes induced by tin (IV) chloride Tetrahedron Letters. 31: 6239-6242. DOI: 10.1016/S0040-4039(00)97034-5 |
0.462 |
|
| 1990 |
PARMEE ER, STEEL PG, THOMAS EJ. ChemInform Abstract: A Total Synthesis of Milbemycin E (I). Cheminform. 21. DOI: 10.1002/CHIN.199010329 |
0.6 |
|
| 1989 |
Astles PC, Thomas EJ. Cembranoid Synthesis Using Ketophosphonate - Aldehyde Crclization: Syntheses of Thunbergols and α- and β-Cembra-2,7,11-triene-4,6-diols Synlett. 1989: 42-45. DOI: 10.1055/S-1989-34685 |
0.368 |
|
| 1989 |
Jephcote VJ, Pratt AJ, Thomas EJ. Synthesis of optically active (E)-1-alkoxymethoxybut-2-enyl(tributyl)stannanes: stereochemistry of their thermal reactions with aldehydes Journal of the Chemical Society-Perkin Transactions 1. 1529-1535. DOI: 10.1039/P19890001529 |
0.405 |
|
| 1989 |
Pratt AJ, Thomas EJ. Stereoselective thermal reactions between (E)-1-alkoxymethoxybut-2-enyl-(tributyl)stannanes and aldehydes Journal of the Chemical Society-Perkin Transactions 1. 1521-1527. DOI: 10.1039/P19890001521 |
0.465 |
|
| 1989 |
Sauter R, Thomas EJ, Watts JP. Cytochalasan synthesis: an alternative approach to cytochalasin H Journal of the Chemical Society-Perkin Transactions 1. 519-523. DOI: 10.1039/P19890000519 |
0.41 |
|
| 1989 |
Thomas EJ, Whitehead JWF. Cytochalasan synthesis: total synthesis of cytochalasin H Journal of the Chemical Society-Perkin Transactions 1. 17: 507-518. DOI: 10.1039/P19890000507 |
0.481 |
|
| 1989 |
Thomas EJ, Whitehead JWF. Cytochalasan synthesis: total synthesis of the naturally occurring [13]cytochalasan proxiphomin Journal of the Chemical Society-Perkin Transactions 1. 499-505. DOI: 10.1039/P19890000499 |
0.529 |
|
| 1989 |
Harkin SA, Jones RH, Tapolczay DJ, Thomas EJ. Cytochalasan synthesis: macrocycle synthesis using intramolecular Diels–Alder reactions. X-Ray crystal structure of 10-phenyl[11]cytochalasa-6(7),13t-diene-1,21-dione Journal of the Chemical Society-Perkin Transactions 1. 489-497. DOI: 10.1039/P19890000489 |
0.45 |
|
| 1989 |
Parmee ER, Steel PG, Thomas EJ. A total synthesis of milbemycin E Journal of the Chemical Society, Chemical Communications. 1250-1253. DOI: 10.1039/C39890001250 |
0.626 |
|
| 1989 |
Savage I, Thomas EJ. Asymmetric α-amino acid synthesis: Synthesis of (+)-polyoxamic acid using a [3,3]allylic trifluoroacetimidate rearrangement Journal of the Chemical Society, Chemical Communications. 717-719. DOI: 10.1039/C39890000717 |
0.404 |
|
| 1989 |
Munt SP, Thomas EJ. Stereoselective exocyclic double bond formation via vinyl radical cyclization Journal of the Chemical Society, Chemical Communications. 480-482. DOI: 10.1039/C39890000480 |
0.361 |
|
| 1989 |
Chambers MS, Thomas EJ. Total synthesis of (5S)-thiolactomycin: Revision of the absolute configuration of the natural product Journal of the Chemical Society, Chemical Communications. 23-24. DOI: 10.1039/C39890000023 |
0.386 |
|
| 1989 |
Craven AP, Dyke HJ, Thomas EJ. Cytochalasan syntheses: Synthesis of (17, 18)-17, 18-dihydroxy-10-(prop-2-YL)-14-methyl-[11]cytochalasa-6(7), 13z, 19E-triene-1, 21-dione; an isomer of aspochalasin C Tetrahedron. 45: 2417-2429. DOI: 10.1016/S0040-4020(01)83439-6 |
0.465 |
|
| 1989 |
Hull C, Mortlock SV, Thomas EJ. On the stereoselectivity of reaction between α-methylbut-2-enylstannanes and aldehydes Tetrahedron. 45: 1007-1015. DOI: 10.1016/0040-4020(89)80012-2 |
0.445 |
|
| 1989 |
CRAVEN AP, DYKE HJ, THOMAS EJ. ChemInform Abstract: Cytochalasan Synthesis: Synthesis of (17S,18S)-17,18-Dihydroxy-10-(prop-2-yl)-14-methyl-(11)cytochalasa-6(7),13Z,19E-triene-1,21-dione, an Isomer of Aspochalasin C. Cheminform. 20. DOI: 10.1002/CHIN.198933336 |
0.4 |
|
| 1989 |
HULL C, MORTLOCK SV, THOMAS EJ. ChemInform Abstract: Stereoselectivity of Reactions Between α-Methylbut-2-enylstannanes and Aldehydes. Cheminform. 20. DOI: 10.1002/CHIN.198927137 |
0.316 |
|
| 1988 |
Mortlock SV, Seckington JK, Thomas EJ. An approach to (8,3′)- and (8,5′·7,3′)-neolignans Journal of the Chemical Society-Perkin Transactions 1. 2305-2307. DOI: 10.1039/P19880002305 |
0.324 |
|
| 1988 |
Mortlock SV, Thomas EJ. An observation of diastereoface selectivity in thermal reactions between δ-alkoxyallylstannanes and aldehydes Tetrahedron Letters. 29: 2479-2482. DOI: 10.1016/S0040-4039(00)87912-5 |
0.339 |
|
| 1987 |
Merifield E, Steel PG, Thomas EJ. Asymmetric synthesis of milbemycin and avermectin spiroacetals Journal of the Chemical Society, Chemical Communications. 1826-1828. DOI: 10.1039/C39870001826 |
0.647 |
|
| 1987 |
Chambers MS, Thomas EJ, Williams DJ. An asymmetric synthesis of thiotetronic acids using chirality transfer via an allyl xanthate-to-dithiocarbonate rearrangement. X-Ray crystal structure of (5R)-2,5-dihydro-4-hydroxy-5-methyl-3-phenyl-5-prop-1′-enyl-2-oxothiophene Journal of the Chemical Society, Chemical Communications. 1228-1230. DOI: 10.1039/C39870001228 |
0.394 |
|
| 1987 |
Thomas EJ, Williams AC. A stereoselective approach to the δ-lactone fragment of the lankacidin antibiotics Journal of the Chemical Society, Chemical Communications. 992-994. DOI: 10.1039/C39870000992 |
0.368 |
|
| 1987 |
Mortlock SV, Stacey NA, Thomas EJ. Regioselectivity of selenoxide elimination: synthesis of the cyclohexenediol fragment of non-aromatic β-milbemycins Journal of the Chemical Society, Chemical Communications. 880-881. DOI: 10.1039/C39870000880 |
0.387 |
|
| 1987 |
Khandekar G, Robinson GC, Stacey NA, Steel PG, Thomas EJ, Vather S. Asymmetric synthesis of the spiroacetal fragment of milbemycin E Journal of the Chemical Society, Chemical Communications. 877-880. DOI: 10.1039/C39870000877 |
0.655 |
|
| 1987 |
Hull C, Mortlock SV, Thomas EJ. Stereoselective synthesis of Z-alkenes from α-methylcrotylstannanes and aldehydes Tetrahedron Letters. 28: 5343-5346. DOI: 10.1016/S0040-4039(00)96725-X |
0.42 |
|
| 1986 |
Sauter R, Thomas EJ, Watts JP. Cytochalasan synthesis: An alternative approach to cytochalasin H Journal of the Chemical Society, Chemical Communications. 1449-1450. DOI: 10.1039/C39860001449 |
0.31 |
|
| 1986 |
Dyke H, Sauter R, Steel P, Thomas EJ. Cytochalasan synthesis: total synthesis of cytochalasin G Journal of the Chemical Society, Chemical Communications. 1447-1449. DOI: 10.1039/C39860001447 |
0.64 |
|
| 1986 |
Thomas EJ, Whitehead JWF. Cytochalasan synthesis: Synthesis of an [11]-membered ring precursor of cytochalasin H Journal of the Chemical Society, Chemical Communications. 724-726. DOI: 10.1039/C39860000724 |
0.443 |
|
| 1986 |
Thomas EJ, Whitehead JWF. Cytochalasan Synthesis: Synthesis of an [11]-Membered Ring Precursor of Cytochalasin H. Cheminform. 17. DOI: 10.1002/Chin.198640330 |
0.413 |
|
| 1986 |
Fray MJ, Thomas EJ, Williams DJ. Stereoselective Addition of Benzonitrile Oxide and N-Benzyl-C-phenylnitrone to (5RS,6SR)-5,6-Dihydro-6-ethyl-5-methylpyran-2(2H)-one. Cheminform. 17. DOI: 10.1002/Chin.198617233 |
0.359 |
|
| 1986 |
Fray MJ, Jones RH, Thomas EJ. The Stereoselectivity of Addition of N-Benzyl-C-alkylnitrones to Methyl Crotonate. Cheminform. 17. DOI: 10.1002/Chin.198617232 |
0.378 |
|
| 1985 |
Fray MJ, Thomas EJ, Williams DJ. Stereoselective addition of benzonitrile oxide and N-benzyl-C-phenylnitrone to (5RS,6SR)-5,6-dihydro-6-ethyl-5-methylpyran-2(2H)-one. Crystal structure of (1RS,4RS,5RS,6RS,9SR)-8-benzyl-1,5-dimethyl-4-ethyl-9-phenyl-3,7-dioxa-8-azabicyclo [4.3.0]nonan-2-one. Journal of the Chemical Society-Perkin Transactions 1. 2763-2767. DOI: 10.1039/P19850002763 |
0.387 |
|
| 1985 |
Fray MJ, Jones RH, Thomas EJ. The stereoselectivity of addition of N-benzyl-C-alkylnitrones to methyl crotonate. X-ray crystal structure of (3RS,4SR,5RS)-2-benzyl-4-methoxy-carbonyl-5-methyl-3-[(4RS)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]isoxazolidine Journal of the Chemical Society-Perkin Transactions 1. 2753-2761. DOI: 10.1039/P19850002753 |
0.438 |
|
| 1985 |
Hughes MJ, Thomas EJ, Turnbull MD, Jones RH, Warner RE. Synthesis of a macrocyclic analogue of milbemycin β1; X-ray structure of (1RS, 4RS, 6SR, 7SR, 19RS)-(10Z, 12E, 16E)-6,16-dimethyl-9-hydroxy-7-methoxy-10-methoxycarbonyl-2-oxatricyclo[17.3.1.04,9]tricosa-10,12,16-trien-3-one Journal of the Chemical Society, Chemical Communications. 755-758. DOI: 10.1039/C39850000755 |
0.4 |
|
| 1985 |
Craven A, Tapolczay DJ, Thomas EJ, Whitehead JWF. An approach to cytochalasin D; 11-membered ring formation using an intramolecular Diels–Alder reaction Journal of the Chemical Society, Chemical Communications. 145-147. DOI: 10.1039/C39850000145 |
0.444 |
|
| 1985 |
Tapolczay DJ, Thomas EJ, Whitehead JWF. Total synthesis of proxiphomin, a naturally occurring [13]cytochalasan Journal of the Chemical Society, Chemical Communications. 143-145. DOI: 10.1039/C39850000143 |
0.491 |
|
| 1985 |
Jephcote VJ, Thomas EJ. Regioselective synthesis of α-substituted allyl- and homoallyl-stannanes by selenoxide elimination Tetrahedron Letters. 26: 5327-5330. DOI: 10.1016/S0040-4039(00)95030-5 |
0.463 |
|
| 1985 |
Hughes MJ, Thomas EJ, Turnbull MD, Jones RH, Warner RE. SYNTHESIS OF A MACROCYCLIC ANALOG OF MILBEMYCIN β1. X-RAY STRUCTURE OF (1RS,4RS,6SR,7SR,9SR,19RS)-(10Z,12E,16E)-6,16-DIMETHYL-9-HYDROXY-7-METHOXY-10-METHOXYCARBONYL-2-OXATRICYCLO(17.3.1.04,9)TRICOSA-10,12,16-TRIEN-3-ONE Cheminform. 16. DOI: 10.1002/Chin.198541354 |
0.353 |
|
| 1985 |
Tapolczay DJ, Thomas EJ, Whitehead JWF. Total Synthesis Of Proxiphomin, A Naturally Occurring (13)Cytochalasan Cheminform. 16. DOI: 10.1002/Chin.198524359 |
0.402 |
|
| 1985 |
Craven A, Tapolczay DJ, Thomas EJ, Whitehead JWF. An Approach To Cytochalasin D: 11-Membered Ring Formation Using An Intramolecular Diels-Alder Reaction Cheminform. 16. DOI: 10.1002/Chin.198524358 |
0.344 |
|
| 1984 |
Harkin SA, Singh O, Thomas EJ. Approaches to cytochalasan synthesis: preparation and Diels–Alder reactions of 3-alkyl- and 3-acyl-Δ3-pyrrolin-2-ones Journal of the Chemical Society-Perkin Transactions 1. 15: 1489-1499. DOI: 10.1039/P19840001489 |
0.466 |
|
| 1984 |
Durrant ML, Thomas EJ. Generation and Diels–Alder reactions of 3-acyl-3-pyrroline-2,5-diones Journal of the Chemical Society-Perkin Transactions 1. 15: 901-904. DOI: 10.1039/P19840000901 |
0.442 |
|
| 1984 |
Jephcote VJ, Pratt AJ, Thomas EJ. Synthesis and absolute configuration of optically active E-1-Alkoxymethoxybut-2-enyl(tri-n-butyl)stannanes: Stereoselective reactions with aldehydes Journal of the Chemical Society, Chemical Communications. 800-802. DOI: 10.1039/C39840000800 |
0.428 |
|
| 1984 |
Fray MJ, Thomas EJ. An approach to lankacidin synthesis: control of stereochemistry using Δ2-isoxazolines Tetrahedron. 40: 673-680. DOI: 10.1016/S0040-4020(01)91095-6 |
0.345 |
|
| 1984 |
Jones RH, Robinson GC, Thomas EJ. Aspects of nitrile oxide cycloaddition stereoselectivity: Chemistry of 4-cyano-2,2-dimethyl- and 4-cyano-2,2,5,5-tetramethyl-1,3-dioxolane oxides. X-ray structure of (4 RS, 5RS)-4,5-bismethoxy-carbonyl-3-[(4RS)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]-Δ2-isox-azoline Tetrahedron. 40: 177-184. DOI: 10.1016/0040-4020(84)85117-0 |
0.337 |
|
| 1984 |
Jephcote VJ, Pratt AJ, Thomas EJ. Synthesis And Absolute Configuration Of Optically Active E-1-Alkoxymethoxy-2-Butenyltributylstannanes: Stereoselective Reactions With Aldehydes Cheminform. 15. DOI: 10.1002/Chin.198445083 |
0.436 |
|
| 1984 |
Jones RH, Robinson GC, Thomas EJ. Aspects Of Nitrile Oxide Cycloaddition Stereoselectivity: Chemistry Of 4-Cyano-2,2-Dimethyl- And 4-Cyano-2,2,5,5-Tetramethyl-1,3-Dioxolane Oxides. X-Ray Structure Of (4Rs, 5Rs)-4,5-Bis(Methoxycarbonyl)-3-((4Rs)-2,2,5,5-Tetramethyl-1,3 Cheminform. 15. DOI: 10.1002/Chin.198418207 |
0.317 |
|
| 1983 |
Bailey SJ, Thomas EJ, Vather SM, Wallis J. An approach to cytochalasan synthesis: macrolide formation by an intramolecular Diels-Alder reaction. X-Ray structure of methyl (1RS, 2SR, 5RS, 6RS)-2,5-dimethyl-1-hydroxy-6-[(1RS)-1-hydroxy-2-phenylethyl]cyclohex-3-ene-1-carboxylate Journal of the Chemical Society-Perkin Transactions 1. 14: 851-859. DOI: 10.1039/P19830000851 |
0.373 |
|
| 1983 |
Fray MJ, Thomas EJ, Wallis JD. On the stereoselectivity of epoxide formation using dimethyloxosulphonium methylide. X-Ray structure of (5SR)-5-[(1RS)-1-methyl-2-oxacyclopropyl]pyrrolidin-2-one Journal of the Chemical Society-Perkin Transactions 1. 14: 395-401. DOI: 10.1039/P19830000395 |
0.464 |
|
| 1983 |
Harkin SA, Thomas EJ. Macrocycle formation using intramolecular diels alder reactions: An approach to 'carbocyclic' cytochalasans Tetrahedron Letters. 24: 5535-5538. DOI: 10.1016/S0040-4039(00)94133-9 |
0.366 |
|
| 1983 |
John DI, Tyrrell ND, Thomas EJ. Stereoselective preparation of 6β -substituted penicillanates Tetrahedron. 39: 2477-2484. DOI: 10.1016/S0040-4020(01)92141-6 |
0.318 |
|
| 1982 |
Giddings PJ, John DI, Thomas EJ, Williams DJ. Preparation of 6α-monosubstituted and 6,6-disubstituted penicillanates from 6-diazopenicillanates: reactions of 6-diazopenicillanates with alcohols, thiols, phenylseleninyl compounds, and allylic sulphides, and their analogues Journal of the Chemical Society-Perkin Transactions 1. 14: 2757-2766. DOI: 10.1039/P19820002757 |
0.44 |
|
| 1982 |
Mara AM, Singh O, Thomas EJ, Williams DJ. Tricyclic products from the reaction between penicillin derived thiazoloazetidinones and ethyl diazoacetate. X-Ray structure of methyl 2-[(1R, 3S, 4R, 5S, 6S, 8R)-3-benzyl-4,5-bismethoxycarbonyl-6-ethoxycarbonyl-9-oxo-7,10-diaza-2-thiatricyclo[6.2.0.03,7]decan-10-yl]-3-methylbut-2-enoate Journal of the Chemical Society-Perkin Transactions 1. 2169-2173. DOI: 10.1039/P19820002169 |
0.329 |
|
| 1982 |
Pratt AJ, Thomas EJ. On the use of E-1-methoxymethoxybut-2-enyl(tri-n-butyl)stannane as a threo-selective, homo-enolate equivalent Journal of the Chemical Society - Series Chemical Communications. 1115-1117. DOI: 10.1039/C39820001115 |
0.372 |
|
| 1982 |
John DI, Tyrrell ND, Thomas EJ, Bentely PH, Williams DJ. Reactions of benzyl 6-lsocyanopenicellanate with thiocarbonyl reagents. Novel rearrangements to 2,3-dihydrothiazolo [2,3-b][1,3]-thiazin -5-ones via penam C(5)–C(6) bond cleavage. X-Ray crystal structure and absolute configuration of two rearrangement products Journal of the Chemical Society, Chemical Communications. 76-78. DOI: 10.1039/C39820000076 |
0.385 |
|
| 1982 |
Mara AM, Singh O, Thomas EJ, Williams DJ. Tricyclic Products From The Reaction Between Penicillin Derived Thiazolineazetidinones And Ethyl Diazoacetate. X-Ray Structure Of Methyl 2-((1R,3S,4R,5S,6S,8R)-3-Benzyl-4,5-Bismethoxycarbonyl-6-Ethoxycarbonyl-9-Oxo-7,10-Diaza-2-Thiatr Cheminform. 13. DOI: 10.1002/Chin.198251275 |
0.37 |
|
| 1981 |
John DI, Tyrrell ND, Thomas EJ. Triorganotin hydride reduction of 6β-isothiocyanatopenicillanates: a radical-induced sulphur–C(2) bond cleavage Journal of the Chemical Society, Chemical Communications. 901-902. DOI: 10.1039/C39810000901 |
0.342 |
|
| 1981 |
Baldwin JE, Reed NV, Thomas EJ. Phenylselenylation of arachidonic acid as a route to intermediates for leukotriene synthesis Tetrahedron. 37: 263-267. DOI: 10.1016/0040-4020(81)85063-6 |
0.366 |
|
| 1981 |
BALDWIN JE, REED NV, THOMAS EJ. ChemInform Abstract: PHENYLSELENYLATION OF ARACHIDONIC ACID AS A ROUTE TO INTERMEDIATES FOR LEUKOTRIENE SYNTHESIS. ISOMERIZATION OF CONJUGATED DIENES DURING SELENOXIDE ELIMINATION Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198138149 |
0.329 |
|
| 1980 |
Giddings PJ, D IJ, Thomas EJ. Preparation and reduction of 6-phenylselenylpenicillanates. A stereoselective synthesis of 6β-substituted penicillanates Tetrahedron Letters. 21: 399-402. DOI: 10.1016/S0040-4039(01)85484-8 |
0.303 |
|
| 1980 |
Giddings PJ, D. Ivor J, Thomas EJ. Reactions of 6-diazopenicillanates with allylic sulphides, selenides, and bromides Tetrahedron Letters. 21: 395-398. DOI: 10.1016/S0040-4039(01)85483-6 |
0.311 |
|
| 1980 |
GIDDINGS PJ, JOHN DI, THOMAS EJ. ChemInform Abstract: PREPARATION AND REDUCTION OF 6-PHENYLSELENYLPENICILLANATES. A STEREOSELECTIVE SYNTHESIS OF 6β-SUBSTITUTED PENICILLANATES Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198021321 |
0.312 |
|
| 1980 |
GIDDINGS PJ, JOHN DI, THOMAS EJ. ChemInform Abstract: REACTIONS OF 6-DIAZOPENICILLANATES WITH ALLYLIC SULFIDES, SELENIDES, AND BROMIDES Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198021320 |
0.336 |
|
| 1980 |
MAH T, SIRAT HM, THOMAS EJ. ChemInform Abstract: ASPECTS OF BROMO LACTONE CHEMISTRY. ON THE USE OF BROMO LACTONES IN STEREOSPECIFIC SYNTHESES OF CYCLOHEXENE DERIVATIVES Chemischer Informationsdienst. 11. DOI: 10.1002/CHIN.198015163 |
0.307 |
|
| 1979 |
Denerley PM, Thomas EJ. Preparation of secopenicillanates; preparation of methyl 3-methyl-2-[(2R,3R)-2-methylthio-4-oxo-3-phthalimidoazetidin-1-yl]but-2-enoate Journal of the Chemical Society-Perkin Transactions 1. 11: 3185-3189. DOI: 10.1039/P19790003185 |
0.338 |
|
| 1979 |
Denerley PM, Thomas EJ. Alkylation of penicillanates : aspects of the chemistry of penicillanate sulphonium salts Journal of the Chemical Society-Perkin Transactions 1. 11: 3175-3184. DOI: 10.1039/P19790003175 |
0.413 |
|
| 1979 |
Sirat HM, Thomas EJ, Tyrrell ND. Aspects of the chemistry of methyl 3-hydroxycyclohexa-1,5-diene-1-carboxylate: a methyl benzoate hydrate Journal of the Chemical Society, Chemical Communications. 36-37. DOI: 10.1039/C39790000036 |
0.415 |
|
| 1979 |
MAH T, SIRAT HM, THOMAS EJ. ChemInform Abstract: STEREOSELECTIVITY OF EPOXIDATION OF SUBSTITUTED CYCLOHEXA-1,4-DIENES: INFLUENCE OF AN ALLYLIC METHOXYCARBONYL GROUP Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197952076 |
0.302 |
|
| 1979 |
Sirat HM, Thomas EJ, Tyrrell ND. Aspects Of The Chemistry Of Methyl 3-Hydroxycyclohexa-1,5-Diene-1-Carboxylate: A Methyl Benzoate Hydrate Cheminform. 10. DOI: 10.1002/Chin.197919202 |
0.334 |
|
| 1978 |
Bailey SJ, Thomas EJ, Turner WB, Jarvis JAJ. Approaches to cytochalasan synthesis: macrocycle formation using an intramolecular Diels–Alder reaction Journal of the Chemical Society, Chemical Communications. 474-475. DOI: 10.1039/C39780000474 |
0.468 |
|
| 1978 |
Bailey SJ, Thomas EJ, Turner WB, Jarvis JAJ. Approaches To Cytochalasan Synthesis- Macrocycle Formation Using An Intramolecular Diels-Alder Reaction Cheminform. 9. DOI: 10.1002/Chin.197839224 |
0.468 |
|
| 1976 |
Fleming I, Kemp-Jones AV, Long WE, Thomas EJ. Cyclobutanol: fragmentation ratios for the singlet and triplet excited states in the type II photochemistry of some α-alkylated cyclohexanones Journal of the Chemical Society-Perkin Transactions 1. 7: 7-14. DOI: 10.1039/P29760000007 |
0.341 |
|
| 1974 |
Jones M, Temple P, Thomas EJ, Whitham GH. Synthesis of olefins by base-induced fragmentation of 2-phenyl-1,3-oxathiolans Journal of the Chemical Society, Perkin Transactions 1. 433-436. DOI: 10.1039/P19740000433 |
0.689 |
|
| 1973 |
Hines JN, Peagram MJ, Thomas EJ, Whitham GH. Some reactions of benzaldehyde acetals with alkyl-lithium reagents; a stereospecific olefin synthesis from 1,2-diols Journal of the Chemical Society-Perkin Transactions 1. 5: 2332-2337. DOI: 10.1039/P19730002332 |
0.68 |
|
| 1973 |
THOMAS EJ. ChemInform Abstract: REACTION BETWEEN 2-PHENYL-1,3-BENZODIOXOLE AND N-BUTYL-LITHIUM, AN UNSUCCESSFUL ATTEMPT TO SYNTHESIZE BENZYNE Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/chin.197349209 |
0.31 |
|
| 1972 |
Fleming I, Thomas EJ. The rearrangement of cyclopropyl chlorides to allyl chlorides. Stereospecificity in the recapture of the chloride ion Tetrahedron. 28: 4989-5001. DOI: 10.1016/0040-4020(72)88150-X |
0.545 |
|
| 1971 |
Fleming I, Kemp-Jones AV, Thomas EJ. Cyclobutanol-to-fragmentation ratios for the singlet and triplet states in the photochemistry of cis-2-propyl-4-t-butylcyclohexanone Journal of the Chemical Society D: Chemical Communications. 1158-1159. DOI: 10.1039/C29710001158 |
0.34 |
|
| 1971 |
Fleming I, Thomas EJ. The rearrangement of cyclopropyl chlorides to allyl chlorides: stereospecificity in the recapture of the chloride ion Tetrahedron Letters. 12: 2485-2488. DOI: 10.1016/S0040-4039(01)96898-4 |
0.435 |
|
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