| Year |
Citation |
Score |
| 2020 |
Paudel RR, Ridenour JN, Rath NP, Spilling CD. Synthesis of Phosphonomethyl Tetrahydrofurans via the Mori-Tamaru Reaction of Phosphonodienes. Organic Letters. 22: 3830-3834. PMID 32330059 DOI: 10.1021/Acs.Orglett.0C01080 |
0.53 |
|
| 2019 |
Abutokaikah MT, Gnawali GR, Frye JW, Stump CM, Tschampel J, Murphy MJ, Lachance ES, Guan S, Spilling CD, Bythell BJ. Leaving Group Effects in a Series of Electrosprayed CHN Anthracene Derivatives. Journal of the American Society For Mass Spectrometry. PMID 31399941 DOI: 10.1007/S13361-019-02298-0 |
0.356 |
|
| 2019 |
Spilling CD. The Chemistry and Biology of Cyclophostin, the Cyclipostins and Related Compounds. Molecules (Basel, Switzerland). 24. PMID 31315184 DOI: 10.3390/Molecules24142579 |
0.38 |
|
| 2019 |
Gnawali GR, Rath NP, Spilling CD. Synthesis of Phostones via the Palladium-Catalyzed Ring Opening of Epoxy vinyl phosphonates. The Journal of Organic Chemistry. PMID 31140269 DOI: 10.1021/Acs.Joc.9B00905 |
0.526 |
|
| 2018 |
Viljoen A, Richard M, Nguyen PC, Fourquet P, Camoin L, Paudal RR, Gnawali GR, Spilling CD, Cavalier JF, Canaan S, Blaise M, Kremer L. Cyclipostins and Cyclophostin analogs inhibit the antigen 85C from Mycobacterium tuberculosis both in vitro and in vivo. The Journal of Biological Chemistry. PMID 29301937 DOI: 10.1074/Jbc.Ra117.000760 |
0.317 |
|
| 2017 |
Hamper B, Sullivan B, Rath N, Spilling C. A Practical Gram-Scale Synthesis of Acrylohydroxamic Acid Synthesis. 49: 5335-5338. DOI: 10.1055/S-0036-1589103 |
0.402 |
|
| 2016 |
Hamper BC, Mannino MP, Mueller ME, Harrison LT, Spilling CD. Enantioseparation of α-Hydroxyallylphosphonates and Phosphonoallylic Carbonate Derivatives on Chiral Stationary Phases Using Sequential UV, Polarimetric, and Refractive Index Detection. Chirality. PMID 27516372 DOI: 10.1002/Chir.22627 |
0.352 |
|
| 2015 |
Martin BP, Vasilieva E, Dupureur CM, Spilling CD. Synthesis and comparison of the biological activity of monocyclic phosphonate, difluorophosphonate and phosphate analogs of the natural AChE inhibitor cyclophostin. Bioorganic & Medicinal Chemistry. PMID 26585276 DOI: 10.1016/J.Bmc.2015.10.044 |
0.382 |
|
| 2015 |
Sutivisedsak N, Dawadi S, Spilling CD. Trapping Hemiacetals with Phosphono Substituted Palladium π-Allyl Complexes for the Synthesis of Substituted Cyclic Ethers. Tetrahedron Letters. 56: 3534-3537. PMID 26236053 DOI: 10.1016/J.Tetlet.2015.01.050 |
0.84 |
|
| 2015 |
Vasilieva E, Dutta S, Malla RK, Martin BP, Spilling CD, Dupureur CM. Rat hormone sensitive lipase inhibition by cyclipostins and their analogs. Bioorganic & Medicinal Chemistry. 23: 944-52. PMID 25678014 DOI: 10.1016/J.Bmc.2015.01.028 |
0.789 |
|
| 2015 |
Spilling CD, Malla RK. Synthesis of non-racemic α-hydroxyphosphonates via asymmetric phospho-aldol reaction. Topics in Current Chemistry. 361: 83-136. PMID 25467537 DOI: 10.1007/128_2014_583 |
0.823 |
|
| 2015 |
Roy S, Sutivisedsak N, Hamper BC, Lyss AM, Spilling CD. A Practical and Scalable Synthesis of (S)- and (R)-1-(Dimethoxyphosphoryl)allyl Methyl Carbonates Synthesis (Germany). 47: 3669-3672. DOI: 10.1055/S-0035-1560487 |
0.807 |
|
| 2014 |
Paudyal MP, Wu L, Zhang ZY, Spilling CD, Wong CF. A new class of salicylic acid derivatives for inhibiting YopH of Yersinia pestis. Bioorganic & Medicinal Chemistry. 22: 6781-8. PMID 25468042 DOI: 10.1016/J.Bmc.2014.10.042 |
0.773 |
|
| 2014 |
Malla RK, Ridenour JN, Spilling CD. Relay cross metathesis reactions of vinylphosphonates. Beilstein Journal of Organic Chemistry. 10: 1933-41. PMID 25246952 DOI: 10.3762/Bjoc.10.201 |
0.804 |
|
| 2014 |
Sutivisedsak N, Dawadi S, Spilling CD. Trapping hemiacetals with phosphono substituted palladium π-allyl complexes for the synthesis of substituted cyclic ethers Tetrahedron Letters. DOI: 10.1016/j.tetlet.2015.01.050 |
0.818 |
|
| 2013 |
Point V, Malla RK, Carrière F, Canaan S, Spilling CD, Cavalier JF. Enantioselective inhibition of microbial lipolytic enzymes by nonracemic monocyclic enolphosphonate analogues of cyclophostin. Journal of Medicinal Chemistry. 56: 4393-401. PMID 23651298 DOI: 10.1021/Jm4000787 |
0.813 |
|
| 2012 |
Point V, Malla RK, Diomande S, Martin BP, Delorme V, Carriere F, Canaan S, Rath NP, Spilling CD, Cavalier JF. Synthesis and kinetic evaluation of cyclophostin and cyclipostins phosphonate analogs as selective and potent inhibitors of microbial lipases. Journal of Medicinal Chemistry. 55: 10204-19. PMID 23095026 DOI: 10.1021/Jm301216X |
0.794 |
|
| 2012 |
Kottakota SK, Evangelopoulos D, Alnimr A, Bhakta S, McHugh TD, Gray M, Groundwater PW, Marrs EC, Perry JD, Spilling CD, Harburn JJ. Synthesis and biological evaluation of purpurealidin E-derived marine sponge metabolites: aplysamine-2, aplyzanzine A, and suberedamines A and B. Journal of Natural Products. 75: 1090-101. PMID 22620987 DOI: 10.1021/Np300102Z |
0.337 |
|
| 2012 |
Roy S, Spilling CD. An expeditious total synthesis of both diastereoisomeric lipid dihydroxytetrahydrofurans from Notheia anomala. Organic Letters. 14: 2230-3. PMID 22506757 DOI: 10.1021/Ol300597U |
0.501 |
|
| 2011 |
Malla RK, Bandyopadhyay S, Spilling CD, Dutta S, Dupureur CM. The first total synthesis of (±)-cyclophostin and (±)-cyclipostin P: inhibitors of the serine hydrolases acetyl cholinesterase and hormone sensitive lipase. Organic Letters. 13: 3094-7. PMID 21591624 DOI: 10.1021/Ol200991X |
0.767 |
|
| 2011 |
Mydock LK, Spilling CD, Demchenko AV. Concise synthesis of 1,3-di-O-substituted tetrahydropyran derivatives as conformationally stable pyranose mimetics Comptes Rendus Chimie. 14: 301-306. DOI: 10.1016/J.Crci.2010.05.016 |
0.346 |
|
| 2010 |
Roy S, Spilling CD. Synthesis of the C(18)-C(34) fragment of amphidinolide C and the C(18)-C(29) fragment of amphidinolide F. Organic Letters. 12: 5326-9. PMID 21028791 DOI: 10.1021/Ol102345V |
0.337 |
|
| 2010 |
Paudyal MP, Rath NP, Spilling CD. A formal synthesis of the C1-C9 fragment of amphidinolide C employing the Tamaru reaction. Organic Letters. 12: 2954-7. PMID 20527780 DOI: 10.1021/Ol100959A |
0.782 |
|
| 2010 |
Dutta S, Malla RK, Bandyopadhyay S, Spilling CD, Dupureur CM. Synthesis and kinetic analysis of some phosphonate analogs of cyclophostin as inhibitors of human acetylcholinesterase. Bioorganic & Medicinal Chemistry. 18: 2265-74. PMID 20189400 DOI: 10.1016/J.Bmc.2010.01.063 |
0.773 |
|
| 2010 |
VASCONCELOS ICF, RATH NP, SPILLING CD. ChemInform Abstract: New Homochiral Amino-Phosphine Ligands: Application in Asymmetric Palladium-Catalyzed Allylic Alkylation. Cheminform. 29: no-no. DOI: 10.1002/chin.199835142 |
0.308 |
|
| 2010 |
SHABANY H, SPILLING CD. ChemInform Abstract: Substituent Effects in the Reaction of Allyl Trichloroacetimidates with N-Halosuccinimides: Cyclization vs Aza-Claisen Rearrangement. Cheminform. 29: no-no. DOI: 10.1002/chin.199822041 |
0.335 |
|
| 2010 |
BLAZIS VJ, KOELLER KJ, SPILLING CD. ChemInform Abstract: Reactions of Chiral Phosphorus Acid Diamides: The Asymmetric Synthesis of Chiral α-Hydroxy Phosphonamides, Phosphonates, and Phosphonic Acids. Cheminform. 26: no-no. DOI: 10.1002/chin.199532183 |
0.394 |
|
| 2010 |
MARPLES BA, SPILLING CD. ChemInform Abstract: Intramolecular Ene Reaction of 5-(Prop-2-enyl)-2ξ-hydroxy-5α- cholestan-3-one. Cheminform. 26: no-no. DOI: 10.1002/chin.199519194 |
0.308 |
|
| 2010 |
BLAZIS VJ, KOELLER KJ, SPILLING CD. ChemInform Abstract: Asymmetric Synthesis of α-Hydroxy-Phosphonamides, Phosphonates and Phosphonic Acids. Cheminform. 25: no-no. DOI: 10.1002/chin.199434194 |
0.324 |
|
| 2010 |
MARZABADI CH, SPILLING CD. ChemInform Abstract: Stereoselective Glucal Epoxide Formation. Cheminform. 24: no-no. DOI: 10.1002/chin.199342267 |
0.312 |
|
| 2010 |
BLAZIS V, DE LA CRUZ A, KOELLER K, SPILLING CD. ChemInform Abstract: Reactions of Chiral Phosphorous Acid Diamides Cheminform. 24: no-no. DOI: 10.1002/chin.199335240 |
0.358 |
|
| 2010 |
MARPLES BA, SPILLING CD. ChemInform Abstract: Facile Intramolecular Ene Reactions of Steroidal Unsaturated Acyloins. Cheminform. 23: no-no. DOI: 10.1002/chin.199237278 |
0.344 |
|
| 2010 |
KOELLER KJ, SPILLING CD. ChemInform Abstract: The Preparation and Reactions of Chiral Phosphorous Acid Diamides. Cheminform. 23: no-no. DOI: 10.1002/chin.199226231 |
0.38 |
|
| 2009 |
He A, Sutivisedsak N, Spilling CD. Stereoselective synthesis of cyclic ethers via the palladium-catalyzed intramolecular addition of alcohols to phosphono allylic carbonates. Organic Letters. 11: 3124-7. PMID 19586068 DOI: 10.1021/Ol900980S |
0.822 |
|
| 2009 |
Ley SV, Tackett MN, Maddess ML, Anderson JC, Brennan PE, Cappi MW, Heer JP, Helgen C, Kori M, Kouklovsky C, Marsden SP, Norman J, Osborn DP, Palomero MA, Pavey JB, ... ... Spilling CD, et al. Total synthesis of rapamycin. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 2874-914. PMID 19204960 DOI: 10.1002/Chem.200801656 |
0.48 |
|
| 2008 |
Bandyopadhyay S, Dutta S, Spilling CD, Dupureur CM, Rath NP. Synthesis and biological evaluation of a phosphonate analog of the natural acetyl cholinesterase inhibitor cyclophostin. The Journal of Organic Chemistry. 73: 8386-91. PMID 18821801 DOI: 10.1021/Jo801453V |
0.827 |
|
| 2008 |
Ley SV, Abad-Somovilla A, Anderson JC, Ayats C, Bänteli R, Beckmann E, Boyer A, Brasca MG, Brice A, Broughton HB, Burke BJ, Cleator E, Craig D, Denholm AA, Denton RM, ... ... Spilling CD, et al. The synthesis of azadirachtin: a potent insect antifeedant. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 10683-704. PMID 18821532 DOI: 10.1002/Chem.200801103 |
0.554 |
|
| 2008 |
Yan B, Spilling CD. Synthesis of cyclopentenones via intramolecular HWE and the palladium-catalyzed reactions of allylic hydroxy phosphonate derivatives. The Journal of Organic Chemistry. 73: 5385-96. PMID 18557652 DOI: 10.1021/Jo8004028 |
0.827 |
|
| 2008 |
Ley S, Abad-Somovilla A, Anderson J, Ayats C, Bänteli R, Beckmann E, Boyer A, Brasca M, Brice A, Broughton H, Burke B, Cleator E, Craig D, Denholm A, Denton R, ... ... Spilling C, et al. Cover Picture: The Synthesis of Azadirachtin: A Potent Insect Antifeedant (Chem. Eur. J. 34/2008) Chemistry - a European Journal. 14: 10503-10503. DOI: 10.1002/Chem.200890139 |
0.514 |
|
| 2007 |
Badkar PA, Rath NP, Spilling CD. Asymmetric synthesis of 2-alkyl-3-phosphonopropanoic acids via P-C bond formation and hydrogenation. Organic Letters. 9: 3619-22. PMID 17691799 DOI: 10.1021/Ol701500S |
0.765 |
|
| 2007 |
Maddess ML, Tackett MN, Watanabe H, Brennan PE, Spilling CD, Scott JS, Osborn DP, Ley SV. Total synthesis of rapamycin. Angewandte Chemie (International Ed. in English). 46: 591-7. PMID 17154218 DOI: 10.1002/Anie.200604053 |
0.524 |
|
| 2005 |
Harburn JJ, Rath NP, Spilling CD. Efficient synthesis of tyrosine-derived marine sponge metabolites via acylation of amines with a coumarin. The Journal of Organic Chemistry. 70: 6398-403. PMID 16050702 DOI: 10.1021/Jo050846R |
0.514 |
|
| 2005 |
De la Cruz A, He A, Thanavaro A, Yan B, Spilling CD, Rath NP. Allylic Hydroxy Phosphonates: Versatile Chiral Building Blocks. Cheminform. 36. DOI: 10.1016/J.Jorganchem.2004.11.019 |
0.784 |
|
| 2005 |
De la Cruz A, He A, Thanavaro A, Yan B, Spilling CD, Rath NP. Allylic hydroxy phosphonates: versatile chiral building blocks Journal of Organometallic Chemistry. 690: 2577-2592. DOI: 10.1016/j.jorganchem.2004.11.019 |
0.748 |
|
| 2004 |
He A, Yan B, Thanavaro A, Spilling CD, Rath NP. Synthesis of nonracemic allylic hydroxy phosphonates via alkene cross metathesis. The Journal of Organic Chemistry. 69: 8643-51. PMID 15575740 DOI: 10.1021/Jo0490090 |
0.761 |
|
| 2004 |
Yan B, Spilling CD. Stereospecific Pd(O)-catalyzed malonate additions to allylic hydroxy phosphonate derivatives: a formal synthesis of (-)-enterolactone. The Journal of Organic Chemistry. 69: 2859-62. PMID 15074940 DOI: 10.1021/Jo035795H |
0.799 |
|
| 2003 |
Rowe BJ, Spilling CD. Stereospecific Pd(0)-catalyzed arylation of an allylic hydroxy phosphonate derivative: formal synthesis of (S)-(+)-ar-turmerone. The Journal of Organic Chemistry. 68: 9502-5. PMID 14629182 DOI: 10.1021/Jo0351318 |
0.426 |
|
| 2002 |
Rowe BJ, Spilling CD. The Synthesis of 1-Hydroxy Phosphonates of High Enantiomeric Excess Using Sequential Asymmetric Reactions: Titanium Alkoxide Catalyzed P--C Bond Formation and Kinetic Resolution Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 1955-1955. DOI: 10.1080/10426500213438 |
0.393 |
|
| 2002 |
Rowe BJ, Scholten J, Spilling CD. Palladium Catalyzed Additions to Allylic Hydroxy Phosphonates: Applications in the Enantioselective Synthesis of Enterolactone and Turmerone Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 1881-1884. DOI: 10.1080/10426500212246 |
0.544 |
|
| 2002 |
Thanavaro A, Spilling CD. Formation of Cyclic Acetals from Allylic Hydroxy Phosphonates via Intramolecular Oxymercuration Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 1583-1586. DOI: 10.1080/10426500212221 |
0.819 |
|
| 2001 |
Boehlow TR, Harburn JJ, Spilling CD. Approaches to the synthesis of some tyrosine-derived marine sponge metabolites: synthesis of verongamine and purealidin N. The Journal of Organic Chemistry. 66: 3111-8. PMID 11325276 DOI: 10.1021/Jo010015V |
0.469 |
|
| 2001 |
Rowe BJ, Spilling CD. The synthesis of 1-hydroxy phosphonates of high enantiomeric excess using sequential asymmetric reactions: titanium alkoxide-catalyzed PC bond formation and kinetic resolution Tetrahedron: Asymmetry. 12: 1701-1708. DOI: 10.1016/S0957-4166(01)00303-2 |
0.423 |
|
| 1999 |
De La Cruz MA, Shabany H, Spilling CD. Stereoselective Reactions of Allylic Hydroxy Phosphonates Phosphorus, Sulfur, and Silicon and the Related Elements. 144: 181-184. DOI: 10.1080/10426509908546212 |
0.517 |
|
| 1999 |
Gróning MD, Rowe BJ, Spilling CD. New Catalysts for the Asymmetric Hydrophosphonylation of Aldehydes1 Phosphorus, Sulfur, and Silicon and the Related Elements. 147: 389-389. DOI: 10.1080/10426509908053674 |
0.452 |
|
| 1999 |
Ley SV, Gutteridge CE, Pape AR, Spilling CD, Zumbrunn C. Chemistry of Insect Antifeedants from Azadirachta indica (Part 22): Functionalisation of the Decalin Fragment of Azadirachtin via a Claisen Rearrangement Reaction Synlett. 1999: 1295-1297. DOI: 10.1055/S-1999-2802 |
0.518 |
|
| 1998 |
Vasconcelos IC, Rath NP, Spilling CD. New homochiral amino-phosphine ligands: application in asymmetric palladium catalyzed allylic alkylation Tetrahedron: Asymmetry. 9: 937-948. DOI: 10.1016/S0957-4166(98)00072-X |
0.429 |
|
| 1998 |
Groaning MD, Rowe BJ, Spilling CD. New homochiral cyclic diol ligands for titanium alkoxide catalyzed phosphonylation of aldehydes Tetrahedron Letters. 39: 5485-5488. DOI: 10.1016/S0040-4039(98)01139-3 |
0.365 |
|
| 1998 |
Shabany H, Spilling CD. Substituent effects in the reaction of allyl trichloroacetimidates with N-halosuccinimides: Cyclization vs aza-Claisen rearrangement Tetrahedron Letters. 39: 1465-1468. DOI: 10.1016/S0040-4039(97)10837-1 |
0.481 |
|
| 1998 |
De La Cruz A, Koeller KJ, Rath NP, Spilling CD, Vasconcelos ICF. The synthesis, structure and properties of diazaphospholes: Reagents and ligands for asymmetric synthesis Tetrahedron. 54: 10513-10524. DOI: 10.1016/S0040-4020(98)00502-X |
0.503 |
|
| 1997 |
Boehlow T, De la Cruz A, Rath NP, Spilling CD. Dimethyl (±)-(1S*,2R*,3S*)-[3-phenyl-1-(N-phenylcarbamoyloxy)-2,3-epoxypropyl]phosphonate Acta Crystallographica Section C Crystal Structure Communications. 53: 1947-1949. DOI: 10.1107/S0108270197010408 |
0.333 |
|
| 1997 |
Boehlow TR, Rath NP, Spilling CD. Methyl 4-Hydroxy-3-[4-methoxy-2-(methoxymethyleneoxy)phenyl]-2-{[4-methoxy-2-(methoxymethyleneoxy)phenyl]methyl}-5-oxo-2,5-dihydrofuran-2-carboxylate Acta Crystallographica Section C Crystal Structure Communications. 53: 92-95. DOI: 10.1107/S0108270196011602 |
0.374 |
|
| 1997 |
Kozlowski JS, Marzabadi CH, Rath NP, Spilling CD. Chemistry of glucal halohydrins(II): An unusual protecting group effect in the competitive formation of formyl furanosides and methyl glycosides Carbohydrate Research. 300: 301-313. DOI: 10.1016/S0008-6215(97)00054-2 |
0.325 |
|
| 1996 |
Boehlow TR, Spilling CD. The regio- and stereo- selective epoxidation of alkenes with methyl trioxorhenium and urea-hydrogen peroxide adduct Tetrahedron Letters. 37: 2717-2720. DOI: 10.1016/0040-4039(96)00423-6 |
0.33 |
|
| 1995 |
Blazis VJ, Koeller KJ, Rath NP, Spilling CD. A Chiral Bicyclic 1-Acetoxy Phosphonamide Acta Crystallographica Section C Crystal Structure Communications. 51: 86-88. DOI: 10.1107/S0108270194007948 |
0.333 |
|
| 1995 |
Boehlow TR, Spilling CD. An Efficient Biomimetic Synthesis of Some Marine Sponge Tyrosine Metabolites Natural Product Letters. 7: 1-6. DOI: 10.1080/10575639508043179 |
0.467 |
|
| 1995 |
Koeller KJ, Rath NP, Spilling CD. REACTIONS OF CHIRAL PHOSPHORUS ACID DIAMIDES: LEWIS ACID CATALYZED ADDITION TO IMINES AND OXIDATION WITH SnCl4 Phosphorus, Sulfur, and Silicon and the Related Elements. 103: 171-181. DOI: 10.1080/10426509508027375 |
0.448 |
|
| 1995 |
Blazis VJ, Koeller KJ, Spilling CD. Reactions of chiral phosphorous acid diamides: The asymmetric synthesis of chiral α-hydroxy phosphonamides, phosphonates, and phosphonic acids The Journal of Organic Chemistry. 60: 931-940. DOI: 10.1080/10426509308037389 |
0.499 |
|
| 1995 |
Blazis VJ, Koeller KJ, Spilling CD. Reactions of Chiral Phosphorous Acid Diamides: The Asymmetric Synthesis of Chiral .alpha.-Hydroxy Phosphonamides, Phosphonates, and Phosphonic Acids The Journal of Organic Chemistry. 60: 931-940. DOI: 10.1021/Jo00109A025 |
0.46 |
|
| 1995 |
Kozlowski JK, Rath NP, Spilling CD. Determination of the enantiomeric purity and absolute configuration of α-hydroxy phosphonates Tetrahedron. 51: 6385-6396. DOI: 10.1016/0040-4020(95)00308-U |
0.382 |
|
| 1994 |
Rath NP, Spilling CD. The enantioselective addition of dialkylphosphites to aldehydes: Catalysis by a lanthanum binaphthoxide complex Tetrahedron Letters. 35: 227-230. DOI: 10.1016/S0040-4039(00)76517-8 |
0.423 |
|
| 1994 |
Marzabadi CH, Spilling CD, Tyler LM. The chemistry of glucal halohydrins: The effect of the halide on epoxide formation Tetrahedron. 50: 6783-6796. DOI: 10.1016/S0040-4020(01)81332-6 |
0.401 |
|
| 1994 |
Blazis VJ, Koeller KJ, Spilling CD. Asymmetric synthesis of α-hydroxy- phosphonamides, phosphonates and phosphonic acids Tetrahedron: Asymmetry. 5: 499-502. DOI: 10.1016/0957-4166(94)80002-2 |
0.437 |
|
| 1993 |
Koeller KJ, Rath NP, Spilling CD. Structure of a chiral bicyclic 1-hydroxyalkyl phosphonamide Acta Crystallographica Section C Crystal Structure Communications. 49: 1547-1549. DOI: 10.1107/S0108270193001507 |
0.372 |
|
| 1993 |
Koeller KJ, Rath NP, Spilling CD. Structure of a chiral monocyclic phosphonamide Acta Crystallographica Section C Crystal Structure Communications. 49: 1199-1201. DOI: 10.1107/S0108270192013003 |
0.314 |
|
| 1993 |
Marzabadi CH, Spilling CD. Stereoselective glucal epoxide formation The Journal of Organic Chemistry. 58: 3761-3766. DOI: 10.1021/Jo00066A032 |
0.423 |
|
| 1992 |
Marples BA, Spilling CD. Facile intramolecular ene reactions of steroidal unsaturated acyloins Tetrahedron. 48: 4017-4026. DOI: 10.1016/S0040-4020(01)88481-7 |
0.327 |
|
| 1991 |
Koeller KJ, Spilling CD. The preparation and reactions of chiral phosphorous acid diamides Tetrahedron Letters. 32: 6297-6300. DOI: 10.1016/0040-4039(91)80151-U |
0.47 |
|
| 1990 |
Barrett AGM, Barta TE, Flygare JA, Sabat M, Spilling CD. Approaches to avermectin assembly. A concise stereospecific synthesis of the hexahydrobenzofuran entity The Journal of Organic Chemistry. 55: 2409-2414. DOI: 10.1021/Jo00295A032 |
0.354 |
|
| 1990 |
BARRETT AGM, FLYGARE JA, SPILLING CD. ChemInform Abstract: Stereoselective Syntheses of S-Phenyl Tetrahydrofuran-2-thiocarboxylate and Tetrahydropyran-2-thiocarboxylate Derivatives Using (Phenylthio)nitromethane. Cheminform. 21. DOI: 10.1002/chin.199009179 |
0.302 |
|
| 1989 |
Barrett AGM, Flygare JA, Spilling CD. Stereoselective syntheses of S-phenyl tetrahydrofuran-2-thiocarboxylate and tetrahydropyran-2-thiocarboxylate derivatives using (phenylthio)nitromethane The Journal of Organic Chemistry. 54: 4723-4726. DOI: 10.1021/Jo00280A058 |
0.493 |
|
| 1989 |
Barrett AGM, Robyr C, Spilling CD. Dichloroisopropoxytitanium nitronates as reagents for stereoselective Henry reactions The Journal of Organic Chemistry. 54: 1233-1234. DOI: 10.1021/Jo00267A001 |
0.435 |
|
| 1989 |
Barrett AGM, Cheng MC, Spilling CD, Taylor SJ. (Benzyloxy)nitromethane: a new reagent in bicyclic .beta.-lactam synthesis The Journal of Organic Chemistry. 54: 992-994. DOI: 10.1021/Jo00265A054 |
0.33 |
|
| 1989 |
Barrett AGM, Cheng MC, Sakdarat S, Spilling CD, Taylor SJ. Stereocontrolled total synthesis of the penicillanate ester (2S,5R)-benzyl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylate Tetrahedron Letters. 30: 2349-2350. DOI: 10.1016/S0040-4039(01)80395-6 |
0.387 |
|
| 1989 |
BARRETT AGM, ROBYR C, SPILLING CD. ChemInform Abstract: Dichloroisopropoxytitanium Nitronates as Reagents for Stereoselective Henry Reactions. Cheminform. 20. DOI: 10.1002/chin.198935166 |
0.341 |
|
| 1988 |
Brown DS, Marples BA, Spilling CD. Intramolecular ene reaction of the unsaturated acyloin 3-(but-3-enyl)-2-hydroxy-3-methylcyclohexanone Journal of the Chemical Society-Perkin Transactions 1. 2033-2036. DOI: 10.1039/P19880002033 |
0.444 |
|
| 1988 |
Barrett AG, Spilling CD. Transfer hydrogenation: A stereospecific method for the conversion of nitro alkanes into amines Tetrahedron Letters. 29: 5733-5734. DOI: 10.1016/S0040-4039(00)82175-9 |
0.348 |
|
| 1988 |
BROWN DS, MARPLES BA, SPILLING CD. ChemInform Abstract: Intramolecular Ene Reaction of the Unsaturated Acyloin 3-(But-3-enyl)-2-hydroxy-3-methylcyclohexanone. Cheminform. 19. DOI: 10.1002/chin.198844065 |
0.361 |
|
| 1987 |
Marples BA, Spilling CD. The ene reaction of 5-allyl-2ϵ-hydroxy-5α-cholestan-3-one: An unusually facile ene reaction Tetrahedron Letters. 28: 581-584. DOI: 10.1016/S0040-4039(00)95787-3 |
0.453 |
|
| 1987 |
MARPLES BA, SPILLING CD. ChemInform Abstract: The Ene Reaction of 5-Allyl-2ξ-hydroxy-5α-cholestan-3-one: An Unusually Facile Ene Reaction. Cheminform. 18. DOI: 10.1002/chin.198728308 |
0.329 |
|
| 1986 |
MARPLES BA, SPILLING CD. ChemInform Abstract: Ene Reactions of Unsaturated Acyloins. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198617353 |
0.31 |
|
| 1985 |
Marples BA, Spilling CD. Ene reactions of unsaturated acyloins Tetrahedron Letters. 26: 6515-6518. DOI: 10.1016/S0040-4039(00)99041-5 |
0.369 |
|
| Show low-probability matches. |
