| Year |
Citation |
Score |
| 2020 |
Harada K, Ibaragi D, Edazawa Y, Sakashita M, Nakata A, Kubo M, Carter RG, Fukuyama Y. Front Cover: Asymmetric Construction of Vicinal Stereocenters Containing Quaternary and Tertiary Carbons: Application to the Formal Synthesis of (-)-Chenopodene (Eur. J. Org. Chem. 4/2020) European Journal of Organic Chemistry. 2020: 406-406. DOI: 10.1002/Ejoc.202000090 |
0.39 |
|
| 2019 |
Ghosh A, Brueckner AC, Cheong PH, Carter RG. Second-Generation Synthesis of the Northern Fragment of Mandelalide A: Role of π-Stacking on Sharpless Dihydroxylation of cis-Enynes. The Journal of Organic Chemistry. PMID 31264876 DOI: 10.1021/Acs.Joc.9B01153 |
0.447 |
|
| 2019 |
El-Mansy M, Ghosh A, Cheong PH, Carter R. Regioselective lithiation of benzyl imidazole: Synthesis and evaluation of new organocatalysts for trans-diol functionalization. Synthetic Communications. 49: 3131-3139. DOI: 10.1080/00397911.2019.1655766 |
0.445 |
|
| 2019 |
Harada K, Ibaragi D, Edazawa Y, Sakashita M, Nakata A, Kubo M, Carter RG, Fukuyama Y. Asymmetric Construction of Vicinal Stereocenters Containing Quaternary and Tertiary Carbons: Application to the Formal Synthesis of (-)-Chenopodene European Journal of Organic Chemistry. 2020: 420-423. DOI: 10.1002/Ejoc.201901722 |
0.394 |
|
| 2018 |
Ghosh A, Carter RG. Recent Syntheses and Strategies toward Polycyclic Gelsemium Alkaloids. Angewandte Chemie (International Ed. in English). PMID 30378226 DOI: 10.1002/Anie.201807509 |
0.426 |
|
| 2018 |
Li X, Carter RG. Pummerer Cyclization Revisited: Unraveling of Acyl Oxonium Ion and Vinyl Sulfide Pathways. Organic Letters. PMID 30199264 DOI: 10.1021/Acs.Orglett.8B02059 |
0.333 |
|
| 2018 |
Li X, Carter RG. Total Syntheses of Aromatic Abietane Diterpenoids Utilizing Advances in the Pummerer Rearrangement. Organic Letters. PMID 30199260 DOI: 10.1021/Acs.Orglett.8B02060 |
0.531 |
|
| 2018 |
Goswami S, Harada K, El-Mansy MF, Lingampally R, Carter RG. Enantioselective Synthesis of (-)-Halenaquinone. Angewandte Chemie (International Ed. in English). PMID 29920904 DOI: 10.1002/Anie.201805370 |
0.564 |
|
| 2017 |
Wang S, Xiao J, Li J, Xiang H, Wang C, Chen X, Carter RG, Yang H. Discovery of temperature-dependent, autoinductive reversal of enantioselectivity: palladium-mediated [3+3]-annulation of 4-hydroxycoumarins. Chemical Communications (Cambridge, England). PMID 28345081 DOI: 10.1039/C7Cc01610G |
0.475 |
|
| 2017 |
Li X, Cheong PH, Carter RG. Schinortriterpenoids: A Case Study in Synthetic Design. Angewandte Chemie (International Ed. in English). PMID 28097748 DOI: 10.1002/Anie.201609372 |
0.326 |
|
| 2017 |
Saha M, Carter R. Lycopodium Alkaloids: An Intramolecular Michael Reaction Approach Synlett. 28: 2212-2229. DOI: 10.1055/S-0036-1588851 |
0.831 |
|
| 2016 |
Saha M, Li X, Collett ND, Carter RG. Unified Synthesis of 10-Oxygenated Lycopodium Alkaloids: Impact of C10-Stereochemistry on Reactivity. The Journal of Organic Chemistry. PMID 27353498 DOI: 10.1021/Acs.Joc.6B00900 |
0.799 |
|
| 2016 |
Kang JY, Johnston RC, Snyder KM, Cheong PH, Carter RG. Construction of Stereogenic α,α-Disubstituted Cycloalkanones via 1° Amine Thiourea Dual Catalysis: Experimental Scope and Computational Analyses. The Journal of Organic Chemistry. PMID 27095132 DOI: 10.1021/Acs.Joc.6B00280 |
0.729 |
|
| 2016 |
Watanabe K, Li J, Veerasamy N, Ghosh A, Carter RG. Stereoselective, Ag-Catalyzed Cyclizations To Access Polysubstituted Pyran Ring Systems: Synthesis of C1-C12 Subunit of Madeirolide A. Organic Letters. PMID 27031993 DOI: 10.1021/Acs.Orglett.6B00414 |
0.52 |
|
| 2016 |
Veerasamy N, Ghosh A, Li J, Watanabe K, Serrill JD, Ishmael JE, McPhail KL, Carter RG. Enantioselective Total Synthesis of Mandelalide A and Isomandelalide A: Discovery of a Cytotoxic Ring-Expanded Isomer. Journal of the American Chemical Society. PMID 26759923 DOI: 10.1021/Jacs.5B12318 |
0.488 |
|
| 2016 |
Veerasamy N, Carter RG. Synthesis of quinolizidine-containing lycopodium alkaloids and related natural products Tetrahedron. 72: 4989-5001. DOI: 10.1016/J.Tet.2016.06.043 |
0.387 |
|
| 2016 |
El-Mansy MF, Kang JY, Lingampally R, Carter RG. Proline Sulfonamide-Catalyzed, Domino Process for Asymmetric Synthesis of Amino- and Hydroxy-Substituted Bicyclo[2.2.2]octanes European Journal of Organic Chemistry. 2016: 150-157. DOI: 10.1002/Ejoc.201501302 |
0.774 |
|
| 2016 |
El-Mansy MF, Kang JY, Lingampally R, Carter RG. ChemInform Abstract: Proline Sulfonamide-Catalyzed, Domino Process for Asymmetric Synthesis of Amino- and Hydroxy-Substituted Bicyclo[2.2.2]octanes. Cheminform. 47. DOI: 10.1002/CHIN.201621100 |
0.758 |
|
| 2015 |
Harada K, Imai A, Uto K, Carter RG, Kubo M, Hioki H, Fukuyama Y. Synthesis of jiadifenin using Mizoroki–Heck and Tsuji–Trost reactions Tetrahedron. 71: 2199-2209. DOI: 10.1016/J.Tet.2015.02.090 |
0.505 |
|
| 2015 |
Harada K, Imai A, Uto K, Carter RG, Kubo M, Hioki H, Fukuyama Y. ChemInform Abstract: Synthesis of Jiadifenin Using Mizoroki-Heck and Tsuji-Trost Reactions. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201530238 |
0.385 |
|
| 2015 |
Xiao J, Liu Q, Ren J, Liu J, Carter RG, Chen X, Yang H. ChemInform Abstract: Highly Enantioselective Construction of Polycyclic Spirooxindoles by Organocatalytic 1,3-Dipolar Cycloaddition of 2-Cyclohexenone Catalyzed by Proline-Sulfonamide. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201512140 |
0.371 |
|
| 2014 |
Xiao J, Liu Q, Ren J, Liu J, Carter RG, Chen X, Yang H. Highly Enantioselective Construction of Polycyclic Spirooxindoles by Organocatalytic 1,3-Dipolar Cycloaddition of 2-Cyclohexenone Catalyzed by Proline-Sulfonamide European Journal of Organic Chemistry. 2014: 5700-5704. DOI: 10.1002/Ejoc.201402953 |
0.537 |
|
| 2013 |
Mahapatra S, Carter RG. Exploiting hidden symmetry in natural products: total syntheses of amphidinolides C and F. Journal of the American Chemical Society. 135: 10792-803. PMID 23845005 DOI: 10.1021/Ja404796N |
0.79 |
|
| 2013 |
Veerasamy N, Carlson EC, Collett ND, Saha M, Carter RG. Enantioselective approach to quinolizidines: total synthesis of cermizine D and formal syntheses of senepodine G and cermizine C. The Journal of Organic Chemistry. 78: 4779-800. PMID 23627426 DOI: 10.1021/Jo400324T |
0.805 |
|
| 2013 |
Lu L, Zhang W, Nam S, Horne DA, Jove R, Carter RG. Amphidinolide B: total synthesis, structural investigation, and biological evaluation. The Journal of Organic Chemistry. 78: 2213-47. PMID 23406192 DOI: 10.1021/Jo3026077 |
0.602 |
|
| 2013 |
Saha M, Carter RG. Toward a unified approach for the lycopodines: synthesis of 10-hydroxylycopodine, deacetylpaniculine, and paniculine. Organic Letters. 15: 736-9. PMID 23384410 DOI: 10.1021/Ol303272W |
0.829 |
|
| 2012 |
McIntosh ML, Naffziger MR, Ashburn BO, Zakharov LN, Carter RG. Highly regioselective nitrile oxide dipolar cycloadditions with ortho-nitrophenyl alkynes. Organic & Biomolecular Chemistry. 10: 9204-13. PMID 23090640 DOI: 10.1039/C2Ob26267C |
0.802 |
|
| 2012 |
Mahapatra S, Carter RG. Enantioselective total synthesis of amphidinolide F. Angewandte Chemie (International Ed. in English). 51: 7948-51. PMID 22767517 DOI: 10.1002/Anie.201203935 |
0.81 |
|
| 2012 |
Kang JY, Carter RG. Primary amine, thiourea-based dual catalysis motif for synthesis of stereogenic, all-carbon quaternary center-containing cycloalkanones. Organic Letters. 14: 3178-81. PMID 22668200 DOI: 10.1021/Ol301272R |
0.764 |
|
| 2012 |
Yang H, Banerjee S, Carter RG. Proline sulphonamide-catalysed Yamada-Otani condensation: reaction development, substrate scope and scaffold reactivity. Organic & Biomolecular Chemistry. 10: 4851-63. PMID 22544220 DOI: 10.1039/C2Ob25400J |
0.54 |
|
| 2012 |
Pierce MD, Johnston RC, Mahapatra S, Yang H, Carter RG, Ha-Yeon Cheong P. Mechanism and stereoselectivity of a dual amino-catalyzed robinson annulation: rare duumvirate stereocontrol. Journal of the American Chemical Society. 134: 13624-31. PMID 22540247 DOI: 10.1021/Ja3018219 |
0.799 |
|
| 2012 |
Veerasamy N, Carlson EC, Carter RG. Expedient enantioselective synthesis of cermizine D. Organic Letters. 14: 1596-9. PMID 22372610 DOI: 10.1021/Ol300342N |
0.473 |
|
| 2012 |
McIntosh ML, Johnston RC, Pattawong O, Ashburn BO, Naffziger MR, Cheong PH, Carter RG. Synthesis and computational analysis of densely functionalized triazoles using o-nitrophenylalkynes. The Journal of Organic Chemistry. 77: 1101-12. PMID 22263720 DOI: 10.1021/Jo202467K |
0.79 |
|
| 2012 |
Mahapatra S, Carter RG. Cover Picture: Enantioselective Total Synthesis of Amphidinolide F (Angew. Chem. Int. Ed. 32/2012) Angewandte Chemie International Edition. 51: 7863-7863. DOI: 10.1002/Anie.201205172 |
0.757 |
|
| 2012 |
Mahapatra S, Carter RG. Titelbild: Enantioselective Total Synthesis of Amphidinolide F (Angew. Chem. 32/2012) Angewandte Chemie. 124: 7985-7985. DOI: 10.1002/Ange.201205172 |
0.759 |
|
| 2011 |
Collett ND, Carter RG. Stereoselective synthesis of the eastern quinolizidine portion of himeradine A. Organic Letters. 13: 4144-7. PMID 21749086 DOI: 10.1021/Ol201704G |
0.81 |
|
| 2011 |
Harada K, Imai A, Uto K, Carter RG, Kubo M, Hioki H, Fukuyama Y. Synthesis of the ABC ring system of Jiadifenin via Pd-catalyzed cyclizations. Organic Letters. 13: 988-91. PMID 21265560 DOI: 10.1021/Ol103024Z |
0.47 |
|
| 2011 |
Harada K, Horiuchi H, Tanabe K, Carter RG, Esumi T, Kubo M, Hioki H, Fukuyama Y. Asymmetric synthesis of (−)-chicanine using a highly regioselective intramolecular Mitsunobu reaction and revision of its absolute configuration Tetrahedron Letters. 52: 3005-3008. DOI: 10.1016/J.Tetlet.2011.03.154 |
0.368 |
|
| 2011 |
Harada K, Horiuchi H, Tanabe K, Carter RG, Esumi T, Kubo M, Hioki H, Fukuyama Y. ChemInform Abstract: Asymmetric Synthesis of (-)-Chicanine Using a Highly Regioselective Intramolecular Mitsunobu Reaction and Revision of Its Absolute Configuration. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201138197 |
0.428 |
|
| 2010 |
Yang H, Carter RG. Proline Sulfonamide-Based Organocatalysis: Better Late than Never. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2010: 2827-2838. PMID 21461132 DOI: 10.1055/S-0030-1259020 |
0.53 |
|
| 2010 |
Yang H, Mahapatra S, Cheong PH, Carter RG. Highly stereoselective and scalable anti-aldol reactions using N-(p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: scope and origins of stereoselectivities. The Journal of Organic Chemistry. 75: 7279-90. PMID 20932013 DOI: 10.1021/Jo1015008 |
0.778 |
|
| 2010 |
Collett N, Carter RG. Synthetic strategy: Moving backwards in new ways. Nature Chemistry. 2: 613-4. PMID 20651720 DOI: 10.1038/Nchem.758 |
0.771 |
|
| 2010 |
Yang H, Carter RG. Development of an enantioselective route toward the Lycopodium alkaloids: total synthesis of lycopodine. The Journal of Organic Chemistry. 75: 4929-38. PMID 20586477 DOI: 10.1021/Jo100916X |
0.61 |
|
| 2010 |
Yang H, Carter RG. Synthesis of all-carbon, quaternary center-containing cyclohexenones through an organocatalyzed, multicomponent coupling. Organic Letters. 12: 3108-11. PMID 20527905 DOI: 10.1021/Ol1011955 |
0.55 |
|
| 2010 |
Yang H, Carter RG. Organocatalyzed, enantioselective synthesis of bicyclo-[2.2.2]-octanes containing benzylic, all-carbon quaternary centers Tetrahedron. 66: 4854-4859. DOI: 10.1016/J.Tet.2010.01.094 |
0.521 |
|
| 2010 |
Carter RG, Graves DE. ChemInform Abstract: Studies Directed Toward the Total Synthesis of Azaspiracid. Construction of the C1-C19 (I) Carbon Backbone and Synthesis of the C10, C13 Nonnatural Transoidal Bisspirocyclic Ring System (II). Cheminform. 33: no-no. DOI: 10.1002/CHIN.200202254 |
0.359 |
|
| 2010 |
MAGNUS P, CARTER R, DAVIES M, ELLIOTT J, PITTERNA T. ChemInform Abstract: Studies on the Synthesis of the Core Structures of the Antitumor Agents Neocarzinostatin, Kedarcidin, C-1027 and Maduropeptin. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199632304 |
0.312 |
|
| 2009 |
Mahapatra S, Carter RG. Efficient synthesis of the C(7)-C(20) subunit of amphidinolides C and F. Organic & Biomolecular Chemistry. 7: 4582-5. PMID 19865690 DOI: 10.1039/B916744G |
0.784 |
|
| 2009 |
Yang H, Carter RG. Asymmetric construction of nitrogen-containing [2.2.2] bicyclic scaffolds using N-( p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide. The Journal of Organic Chemistry. 74: 5151-6. PMID 19743541 DOI: 10.1021/Jo9009062 |
0.485 |
|
| 2009 |
Yang H, Carter RG. Enantioselective Mannich reactions with the practical proline mimetic N-(p-dodecylphenyl-sulfonyl)-2-pyrrolidinecarboxamide. The Journal of Organic Chemistry. 74: 2246-9. PMID 19193123 DOI: 10.1021/Jo8027938 |
0.482 |
|
| 2009 |
Lu L, Zhang W, Carter RG. Synthesis of Amphidinolides B1 and B2 Synfacts. 2009: 474-474. DOI: 10.1055/S-0028-1088166 |
0.316 |
|
| 2008 |
Yang H, Carter RG. N-(p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: a practical proline mimetic for facilitating enantioselective aldol reactions. Organic Letters. 10: 4649-52. PMID 18808137 DOI: 10.1021/Ol801941J |
0.448 |
|
| 2008 |
Ashburn BO, Carter RG, Zakharov LN. Diels-Alder approach to biaryls: elucidation of competing tandem [2+2] cycloaddition/[1,3] sigmatropic shift pathway. The Journal of Organic Chemistry. 73: 7305-9. PMID 18722410 DOI: 10.1021/Jo801245A |
0.782 |
|
| 2008 |
Yang H, Carter RG, Zakharov LN. Enantioselective total synthesis of lycopodine. Journal of the American Chemical Society. 130: 9238-9. PMID 18582046 DOI: 10.1021/Ja803613W |
0.634 |
|
| 2008 |
Carlson EC, Rathbone LK, Yang H, Collett ND, Carter RG. Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid. The Journal of Organic Chemistry. 73: 5155-8. PMID 18529081 DOI: 10.1021/Jo800749T |
0.802 |
|
| 2008 |
Lu L, Zhang W, Carter RG. Total synthesis of cytotoxic macrolide amphidinolide B1 and the proposed structure of amphidinolide B2. Journal of the American Chemical Society. 130: 7253-5. PMID 18489095 DOI: 10.1021/Ja803012N |
0.573 |
|
| 2008 |
Perkins JR, Carter RG. Synthesis of programmable tetra-ortho-substituted biaryl compounds using Diels-Alder cycloadditions/cycloreversions of disubstituted alkynyl stannanes. Journal of the American Chemical Society. 130: 3290-1. PMID 18298122 DOI: 10.1021/Ja7113486 |
0.495 |
|
| 2008 |
Ashburn BO, Carter RG. Diels-Alder approach to biaryls (DAB): importance of the ortho-nitro moiety in the [4 + 2] cycloaddition. Organic & Biomolecular Chemistry. 6: 255-7. PMID 18174991 DOI: 10.1039/B714893C |
0.8 |
|
| 2008 |
Carter R, Yang H, Vasudevan S, Oriakhi C, Shields J. Scalable Synthesis of Lissamine Rhodamine B Sulfonyl Chloride and Incorporation of Xanthene Derivatives onto Polymer Supports Synthesis. 2008: 957-961. DOI: 10.1055/S-2008-1032172 |
0.425 |
|
| 2008 |
Ashburn BO, Rathbone LK, Camp EH, Carter RG. A Diels–Alder approach to biaryls (DAB): synthesis of the western portion of TMC-95 Tetrahedron. 64: 856-865. DOI: 10.1016/J.Tet.2007.10.118 |
0.811 |
|
| 2007 |
Ashburn BO, Carter RG. Diels-Alder approach to tetra-ortho-substituted biaryls employing propargylic tertiary alcohols as dienophiles. The Journal of Organic Chemistry. 72: 10220-3. PMID 17602533 DOI: 10.1021/Jo070812E |
0.805 |
|
| 2007 |
Naffziger MR, Ashburn BO, Perkins JR, Carter RG. Diels-Alder approach for the construction of halogenated, o-nitro biaryl templates and application to the total synthesis of the anti-HIV agent siamenol. The Journal of Organic Chemistry. 72: 9857-65. PMID 17602532 DOI: 10.1021/Jo070740R |
0.808 |
|
| 2007 |
Ashburn BO, Carter RG, Zakharov LN. Synthesis of tetra-ortho-substituted, phosphorus-containing and carbonyl-containing biaryls utilizing a Diels-Alder approach. Journal of the American Chemical Society. 129: 9109-16. PMID 17602479 DOI: 10.1021/Ja071163R |
0.836 |
|
| 2006 |
Zhou XT, Lu L, Furkert DP, Wells CE, Carter RG. Synthesis of the southern FGHI ring system of azaspiracid-1 and investigation into the controlling elements of C28- and C36-ketalization. Angewandte Chemie (International Ed. in English). 45: 7622-6. PMID 17044107 DOI: 10.1002/Anie.200603353 |
0.593 |
|
| 2006 |
Ashburn BO, Carter RG. Diels-Alder approach to polysubstituted biaryls: rapid entry to tri- and tetra-ortho-substituted phosphorus-containing biaryls. Angewandte Chemie (International Ed. in English). 45: 6737-41. PMID 16977660 DOI: 10.1002/Anie.200602683 |
0.804 |
|
| 2006 |
Zhou XT, Carter RG. Synthesis of the C1-C26 northern portion of azaspiracid-1: kinetic versus thermodynamic control of the formation of the bis-spiroketal. Angewandte Chemie (International Ed. in English). 45: 1787-90. PMID 16470899 DOI: 10.1002/Anie.200503733 |
0.395 |
|
| 2005 |
Zhang W, Carter RG. Synthetic studies toward amphidinolide B1: synthesis of the C9-C26 fragment. Organic Letters. 7: 4209-12. PMID 16146389 DOI: 10.1021/Ol051544E |
0.534 |
|
| 2004 |
Zhou XT, Carter RG. Synthesis of the ABCD and ABCDE ring systems of azaspiracid-1. Chemical Communications (Cambridge, England). 2138-40. PMID 15467841 DOI: 10.1039/B410092A |
0.419 |
|
| 2004 |
Bourland TC, Carter RG, Yokochi AF. Vanadium-catalyzed selenide oxidation with in situ[2,3] sigmatropic rearrangement (SOS reaction): scope and asymmetric applications. Organic & Biomolecular Chemistry. 2: 1315-29. PMID 15105922 DOI: 10.1039/B316502G |
0.689 |
|
| 2004 |
Zhang W, Carter RG, Yokochi AF. Unified synthesis of C19-C26 subunits of amphidinolides B1, B2, and B3 by exploiting unexpected stereochemical differences in Crimmins' and Evans' aldol reactions. The Journal of Organic Chemistry. 69: 2569-72. PMID 15049660 DOI: 10.1021/Jo035829L |
0.735 |
|
| 2003 |
White JD, Carter RG, Sundermann KF, Wartmann M. Total Synthesis of Epothilone B, Epothilone D, andcis- andtrans-9,10-Dehydroepothilone D [J. Am. Chem. Soc.2001,123, 5407−5413]. Journal of the American Chemical Society. 125: 3190-3190. DOI: 10.1021/Ja0251221 |
0.477 |
|
| 2003 |
Carter RG, Bourland T, Zhou X, Gronemeyer MA. Controlling influences in bisspiroketal formation: synthesis of the ABC ring system of azaspiracid Tetrahedron. 59: 8963-8974. DOI: 10.1016/J.Tet.2003.03.003 |
0.396 |
|
| 2002 |
Carter RG, Graves DE, Gronemeyer MA, Tschumper GS. Synthesis of the ABC ring system of azaspiracid. 2. A systematic study into the effect of C16 and C17 substitution on bis-spirocyclization Organic Letters. 4: 2181-2184. PMID 12074662 DOI: 10.1021/Ol026034O |
0.48 |
|
| 2002 |
Carter RG, Bourland TC, Graves DE. Synthesis of the ABC ring system of azaspiracid. 1. Effect of D ring truncation on bis-spirocyclization Organic Letters. 4: 2177-2179. PMID 12074661 DOI: 10.1021/Ol026033W |
0.393 |
|
| 2001 |
White JD, Carter RG, Sundermann KF, Wartmann M. Total synthesis of epothilone B, epothilone D, and cis- and trans-9,10-dehydroepothilone D. Journal of the American Chemical Society. 123: 5407-13. PMID 11389619 DOI: 10.1021/Ja010454B |
0.798 |
|
| 2001 |
Carter RG, Graves DE. Studies directed toward the total synthesis of azaspiracid. Construction of the C1-C19 carbon backbone and synthesis of the C10, C13 nonnatural transoidal bisspirocyclic ring system Tetrahedron Letters. 42: 6035-6039. DOI: 10.1016/S0040-4039(01)01211-4 |
0.437 |
|
| 2000 |
Carter RG, Weldon DJ. Studies Directed toward the Total Synthesis of Azaspiracid: Stereoselective Construction of C1-C12, C13-C19, and C21-C25 Fragments Organic Letters. 2: 3913-3916. PMID 11101452 DOI: 10.1021/Ol006674W |
0.43 |
|
| 2000 |
Carter RG, Bourland TC. The first vanadium-catalyzed oxidation of aryl allylic selenides with in situ [2,3] sigmatropic rearrangement Chemical Communications. 2031-2032. DOI: 10.1039/B006278M |
0.414 |
|
| 2000 |
Carter R, Hodgetts K, McKenna J, Magnus P, Wren S. Studies on the Stereoselective Synthesis of the Marine Antitumor Agent Eleutherobin Tetrahedron. 56: 4367-4382. DOI: 10.1016/S0040-4020(00)00309-4 |
0.651 |
|
| 1999 |
White JD, Carter RG, Sundermann KF. A Highly Stereoselective Synthesis of Epothilone B. The Journal of Organic Chemistry. 64: 684-685. PMID 11674127 DOI: 10.1021/Jo982108R |
0.8 |
|
| 1999 |
White JD, Sundermann KF, Carter RG. Improved synthesis of epothilone B employing alkylation of an alkyne for assembly of subunits. Organic Letters. 1: 1431-4. PMID 10825989 DOI: 10.1021/Ol990248X |
0.825 |
|
| 1996 |
Magnus P, Carter R, Davies M, Elliott J, Pitterna T. Studies on the synthesis of the core structures of the antitumor agents neocarzinostatin, kedarcidin, C-1027 and maduropeptin Tetrahedron. 52: 6283-6306. DOI: 10.1016/0040-4020(96)00283-9 |
0.612 |
|
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