| Year |
Citation |
Score |
| 2021 |
Ward DE, Diddi N. Total Synthesis of Dolabriferol C via a Highly Stereoselective One-Pot Coupling of a Meso 3,7-Diketone with Two Chiral Aldehydes. Angewandte Chemie (International Ed. in English). PMID 34648679 DOI: 10.1002/anie.202111895 |
0.443 |
|
| 2014 |
Ward DE, Kundu D, Biniaz M, Jana S. A systematic study of the effects of relative configuration, protecting group, and enolate type on the diastereoselectivities of aldol reactions of a chiral ethyl ketone with 2-methylpropanal. The Journal of Organic Chemistry. 79: 6868-94. PMID 25029195 DOI: 10.1021/jo500927x |
0.436 |
|
| 2012 |
Ward DE, Zahedi MM. Total synthesis of muamvatin. Organic Letters. 14: 6246-9. PMID 23210898 DOI: 10.1021/ol303004k |
0.45 |
|
| 2012 |
Ward DE, Kazemeini A. Aldol reactions with kinetic resolution: scope and limitations of ketal- and dithioketal-protected β-ketoaldehydes. The Journal of Organic Chemistry. 77: 10789-803. PMID 23137001 DOI: 10.1021/jo302142v |
0.426 |
|
| 2012 |
Becerril-Jiménez F, Ward DE. On the origin of siphonariid polypropionates: total synthesis of caloundrin B and its isomerization to siphonarin B. Organic Letters. 14: 1648-51. PMID 22369698 DOI: 10.1021/ol300432y |
0.62 |
|
| 2011 |
Ward DE. The thiopyran route to polypropionates. Chemical Communications (Cambridge, England). 47: 11375-93. PMID 21761054 DOI: 10.1039/c1cc13323c |
0.448 |
|
| 2011 |
Ward DE, Jheengut V, Beye GE, Gillis HM, Karagiannis A, Becerril-Jimenez F. Enantioselective direct aldol reactions of achiral ketones with racemic enolizable α-substituted aldehydes: Scope and limitations Synlett. 508-512. DOI: 10.1055/s-0030-1259525 |
0.667 |
|
| 2010 |
Beye GE, Ward DE. On the origin of siphonariid polypropionates: total synthesis of baconipyrone A, baconipyrone C, and siphonarin B via their putative common precursor. Journal of the American Chemical Society. 132: 7210-5. PMID 20441190 DOI: 10.1021/ja102356j |
0.379 |
|
| 2010 |
WARD DE, GAI Y. ChemInform Abstract: Synthesis of 10-Methyl-δ4-octalins by Diels-Alder Reactions of 2H-Thiopyran Surrogates for 1-Ethenyl-2-methylcyclohexene. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199752118 |
0.402 |
|
| 2010 |
WARD DE, MAN CC, GUO C. ChemInform Abstract: The Thiopyran Route to Polypropionates Revisited: Selective syn and anti Aldol Reactions via 3,6-Dihydro-4-trimethylsilyloxy-2H-thiopyran. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199730031 |
0.41 |
|
| 2010 |
WARD DE, NIXEY TE, GAI Y, HRAPCHAK MJ, ABAEE MS. ChemInform Abstract: Intramolecular Diels-Alder Reactions of 2H-Thiopyran Dienes. Cheminform. 28: no-no. DOI: 10.1002/chin.199703074 |
0.42 |
|
| 2010 |
WARD DE, LIU Y, RHEE CK. ChemInform Abstract: Enhancing Stereoselectivity from Reactions with Modest Group Selectivity. Cheminform. 25: no-no. DOI: 10.1002/chin.199410073 |
0.412 |
|
| 2010 |
WARD DE, NIXEY TE. ChemInform Abstract: Intramolecular Diels-Alder Reactions of 2H-Thiopyrans. Cheminform. 24: no-no. DOI: 10.1002/chin.199327087 |
0.408 |
|
| 2010 |
WARD DE, GAI Y. ChemInform Abstract: Lewis Acid Mediated Diels-Alder Reactions of 2H-Thiopyrans. Cheminform. 24: no-no. DOI: 10.1002/chin.199314071 |
0.357 |
|
| 2010 |
WARD DE, GAI Y. ChemInform Abstract: exo-Selective Diels-Alder Reactions Mediated by Et2AlCl in the Presence of H2O. Cheminform. 23: no-no. DOI: 10.1002/chin.199241048 |
0.458 |
|
| 2010 |
WARD DE, GAI Y, ZOGHAIB WM. ChemInform Abstract: Diels-Alder Reactions of Activated 2H-Thiopyrans. Cheminform. 23: no-no. DOI: 10.1002/chin.199208072 |
0.356 |
|
| 2009 |
Ward DE, Becerril-Jimenez F, Zahedi MM. Rational design of aldol reactions that proceed via kinetic resolution with switchable enantioselectivity. The Journal of Organic Chemistry. 74: 4447-54. PMID 19449845 DOI: 10.1021/jo900716a |
0.675 |
|
| 2008 |
Pardeshi SG, Ward DE. Enantiospecific total synthesis of lairdinol A. The Journal of Organic Chemistry. 73: 1071-6. PMID 18179239 DOI: 10.1021/jo7024465 |
0.41 |
|
| 2007 |
Jheengut V, Ward DE. The thiopyran route to polypropionates: enantioselective synthesis of membrenone B from racemic fragments. The Journal of Organic Chemistry. 72: 7805-8. PMID 17824659 DOI: 10.1021/jo701546f |
0.512 |
|
| 2007 |
Ward DE, Shen J. Enantioselective total synthesis of cyathin A3. Organic Letters. 9: 2843-6. PMID 17580883 DOI: 10.1021/ol070994z |
0.322 |
|
| 2007 |
Ward DE, Beye GE, Sales M, Alarcon IQ, Gillis HM, Jheengut V. Thiopyran route to polypropionates: exploiting and overcoming double stereodifferentiation and mutual kinetic enantioselection in aldol couplings of chiral fragments. The Journal of Organic Chemistry. 72: 1667-74. PMID 17261069 DOI: 10.1021/jo0622532 |
0.683 |
|
| 2006 |
Ward DE, Jheengut V, Beye GE. Thiopyran route to polypropionates: an efficient synthesis of serricornin. The Journal of Organic Chemistry. 71: 8989-92. PMID 17081039 DOI: 10.1021/jo061747w |
0.33 |
|
| 2006 |
Ward DE, Gillis HM, Akinnusi OT, Rasheed MA, Saravanan K, Sasmal PK. Asymmetric synthesis of hexapropionate synthons by sequential enantiotopic group selective enolization of meso diketones. Organic Letters. 8: 2631-4. PMID 16737331 DOI: 10.1021/ol060802k |
0.488 |
|
| 2005 |
Ward DE, Souweha MS. Catalytic enantioselective Diels-Alder reaction by self-assembly of the components on a Lewis acid template. Organic Letters. 7: 3533-6. PMID 16048335 DOI: 10.1021/ol051262e |
0.451 |
|
| 2005 |
Ward DE, Jheengut V, Akinnusi OT. Enantioselective direct intermolecular aldol reactions with enantiotopic group selectivity and dynamic kinetic resolution. Organic Letters. 7: 1181-4. PMID 15760169 DOI: 10.1021/ol050195l |
0.517 |
|
| 2005 |
Ward DE, Jheengut V. Proline-Catalyzed Asymmetric Aldol Reactions of Tetrahydro-4H-thiopyran-4-one with Aldehydes. Cheminform. 36. DOI: 10.1002/CHIN.200507125 |
0.452 |
|
| 2004 |
Ward DE, Sales M, Sasmal PK. Syn-anti isomerization of aldols by enolization. The Journal of Organic Chemistry. 69: 4808-15. PMID 15230607 DOI: 10.1021/jo049626o |
0.605 |
|
| 2004 |
Ward DE, Gai Y, Qiao Q, Shen J. Synthetic studies on cyathin diterpenes - Total synthesis of (±)-allocyathin B3 Canadian Journal of Chemistry. 82: 254-267. DOI: 10.1139/v03-185 |
0.351 |
|
| 2004 |
Ward DE, Jheengut V. Proline-catalyzed asymmetric aldol reactions of tetrahydro-4H-thiopyran-4-one with aldehydes Tetrahedron Letters. 45: 8347-8350. DOI: 10.1016/j.tetlet.2004.09.061 |
0.452 |
|
| 2004 |
Ward DE, Akinnusi OT, Alarcon IQ, Jheengut V, Shen J, Quail JW. The thiopyran route to polypropionates. Asymmetric synthesis of the building blocks by enantioselective protonation Tetrahedron Asymmetry. 15: 2425-2430. DOI: 10.1016/j.tetasy.2004.06.027 |
0.377 |
|
| 2004 |
Ward DE, Gai Y, Qiao Q, Shen J. Synthetic Studies on Cyathin Diterpenes — Total Synthesis of (.+-.)-Allocyathin B3. Cheminform. 35. DOI: 10.1002/chin.200434199 |
0.322 |
|
| 2002 |
Ward DE, Sales M, Man CC, Shen J, Sasmal PK, Guo C. Influence of the beta-alkoxy group on the diastereoselectivity of Aldol reactions of tetrahydro-4H-thiopyran-4-one with 4-Alkoxytetrahydro-2H-thiopyran-3-carboxaldehydes. The Journal of Organic Chemistry. 67: 1618-29. PMID 11871895 |
0.623 |
|
| 2001 |
Ward DE, Gai Y, Lazny R, Pedras MS. Probing host-selective phytotoxicity: synthesis of destruxin B and several natural analogues. The Journal of Organic Chemistry. 66: 7832-40. PMID 11701043 DOI: 10.1021/Jo015953+ |
0.306 |
|
| 2001 |
Ward DE, Sales M, Sasmal PK. Syn-anti isomerization of aldols by enolization. Organic Letters. 3: 3671-3. PMID 11700109 |
0.663 |
|
| 2001 |
Ward DE, Sales M, Hrapchak MJ. Attempted enantiotopic group selective cyanohydrin formation from α-alkoxy aldehydes by double stereodifferentiation Canadian Journal of Chemistry. 79: 1775-1785. DOI: 10.1139/v01-151 |
0.433 |
|
| 2000 |
Ward DE, Gai Y, Qiao Q. A general approach to cyathin diterpenes. Total synthesis of allocyathin B(3). Organic Letters. 2: 2125-7. PMID 10891246 DOI: 10.1021/ol006026c |
0.386 |
|
| 2000 |
Ward DE, Hrapchak MJ, Sales M. Diastereoselective formation of cyanohydrins from alpha-alkoxy aldehydes Organic Letters. 2: 57-60. PMID 10814245 |
0.635 |
|
| 2000 |
Ward DE, Guo C, Sasmal PK, Man CC, Sales M. Thiopyran route to polypropionates: aldol diastereoselectivity of linear and two-directional iterative homologations Organic Letters. 2: 1325-8. PMID 10810739 DOI: 10.1021/ol005790w |
0.673 |
|
| 1997 |
Ward DE, Gai Y. Synthesis of 10-methyl-Δ4-octalins by Diels–Alder reactions of 2H-thiopyran surrogates for 1-ethenyl-2-methylcyclohexene Canadian Journal of Chemistry. 75: 681-693. DOI: 10.1139/v97-082 |
0.337 |
|
| 1997 |
Ward DE, Man CC, Guo C. The thiopyran route to polypropionates revisited: Selective syn and anti aldol reactions via 3,6-dihydro-4-trimethylsilyloxy-2H-thiopyran Tetrahedron Letters. 38: 2201-2202. DOI: 10.1016/S0040-4039(97)00337-7 |
0.396 |
|
| 1994 |
Ward DE, Liu Y, Rhee CK. Asymmetric synthesis using reactions with modest group selectivity Canadian Journal of Chemistry. 72: 1429-1446. DOI: 10.1139/v94-180 |
0.474 |
|
| 1993 |
Ward DE, Liu Y, Rhee CK. Enhancing Stereoselectivity from Reactions with Modest Group Selectivity Synlett. 1993: 561-563. DOI: 10.1055/s-1993-22528 |
0.399 |
|
| 1993 |
Ward DE, Nixey TE. Intramolecular Diels-Alder reactions of 2H-thiopyrans Tetrahedron Letters. 34: 947-950. DOI: 10.1016/S0040-4039(00)77461-2 |
0.396 |
|
| 1992 |
Ward DE, Gai Y. Lewis acid mediated Diels–Alder reactions of 2H-thiopyrans Canadian Journal of Chemistry. 70: 2627-2634. DOI: 10.1139/v92-331 |
0.37 |
|
| 1992 |
Ward DE, Gai Y. Exo selective diels-alder reactions mediated by Et2AlCl in the presence of H2O Tetrahedron Letters. 33: 1851-1854. DOI: 10.1016/S0040-4039(00)74159-1 |
0.447 |
|
| 1991 |
Ward DE, Gai Y, Zoghaib WM. Diels–Alder reactions of activated 2H-thiopyrans Canadian Journal of Chemistry. 69: 1487-1497. DOI: 10.1139/v91-220 |
0.401 |
|
| 1990 |
Ward DE, Zoghaib WM, Rhee CK, Yuanzhu G. Diels-alder reactions of 2H-thiopyrans Tetrahedron Letters. 31: 845-848. DOI: 10.1016/S0040-4039(00)94643-4 |
0.372 |
|
| 1990 |
WARD DE, ZOGHAIB WM, RHEE CK, GAI Y. ChemInform Abstract: Diels-Alder Reactions of 2H-Thiopyrans. Cheminform. 21. DOI: 10.1002/chin.199044075 |
0.387 |
|
| 1989 |
Ward DE, Rhee CK. Chemoselective reductions with sodium borohydride Canadian Journal of Chemistry. 67: 1206-1211. DOI: 10.1139/v89-182 |
0.348 |
|
| 1989 |
WARD DE, RHEE CK. ChemInform Abstract: Chemoselective Reductions with Sodium Borohydride. Aldehydes vs. Ketones. Cheminform. 20. DOI: 10.1002/chin.198917125 |
0.32 |
|
| 1988 |
Ward DE, Rhee CK. Chemoselective Reductions with Sodium Borohydride. Aldehydes vs. Ketones Synthetic Communications. 18: 1927-1933. DOI: 10.1080/00397918808068259 |
0.327 |
|
| 1982 |
AYER WA, WARD DE, BROWNE LM, DELBAERE LTJ, HOYANO Y. ChemInform Abstract: THE SYNTHESIS OF THE CYATHINS. PART 1. SYNTHESIS OF A TRICYCLIC INTERMEDIATE Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198204191 |
0.312 |
|
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