| Year |
Citation |
Score |
| 2019 |
Gill MA, Manthorpe JM. Development of Palladium-Catalyzed Decarboxylative Allylation of Electron-Deficient Sulfones and Identification of Unusual Side Products. The Journal of Organic Chemistry. PMID 30964285 DOI: 10.1021/Acs.Joc.9B00068 |
0.557 |
|
| 2014 |
Shields SW, Manthorpe JM. Efficient, scalable and economical preparation of tris(deuterium)- and 13C-labelled N-methyl-N-nitroso-p-toluenesulfonamide (Diazald®) and their conversion to labelled diazomethane. Journal of Labelled Compounds & Radiopharmaceuticals. 57: 674-9. PMID 25318972 DOI: 10.1002/Jlcr.3231 |
0.36 |
|
| 2014 |
Manthorpe JM, Kong HI, Palko JW, Gill MA. Reduction of SulfurCarbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon Comprehensive Organic Synthesis: Second Edition. 8: 1031-1085. DOI: 10.1016/B978-0-08-097742-3.00830-2 |
0.489 |
|
| 2014 |
Kong HI, Gill MA, Hrdina AH, Crichton JE, Manthorpe JM. ChemInform Abstract: Reactivity of α-Trifluoromethanesulfonyl Esters, Amides and Ketones: Decarboxylative Allylation, Methylation, and Enol Formation. Cheminform. 45: no-no. DOI: 10.1002/chin.201417054 |
0.603 |
|
| 2013 |
Gill MA, Manthorpe JM. Mild, rapid, and inexpensive microwave-assisted synthesis of allylic and propargylic esters Synthetic Communications. 43: 1460-1468. DOI: 10.1080/00397911.2011.640970 |
0.578 |
|
| 2013 |
Palko JW, Buist PH, Manthorpe JM. A flexible and modular stereoselective synthesis of (9R,10S)-dihydrosterculic acid Tetrahedron: Asymmetry. 24: 165-168. DOI: 10.1016/J.Tetasy.2013.01.003 |
0.338 |
|
| 2013 |
Kong HI, Gill MA, Hrdina AH, Crichton JE, Manthorpe JM. Reactivity of a-trifluoromethanesulfonyl esters, amides and ketones: Decarboxylative allylation, methylation, and enol formation Journal of Fluorine Chemistry. 153: 151-161. DOI: 10.1016/J.Jfluchem.2013.03.020 |
0.63 |
|
| 2013 |
Gill MA, Manthorpe JM. ChemInform Abstract: Mild, Rapid, and Inexpensive Microwave-Assisted Synthesis of Allylic and Propargylic Esters. Cheminform. 44: no-no. DOI: 10.1002/chin.201331037 |
0.617 |
|
| 2011 |
Kong HI, Crichton JE, Manthorpe JM. Stereoselective synthesis of ambiphilic alkenes via regioselective methylation of α-trifluoromethanesulfonyl carbonyl compounds with trimethylsilyldiazomethane Tetrahedron Letters. 52: 3714-3717. DOI: 10.1016/J.Tetlet.2011.05.015 |
0.48 |
|
| 2011 |
Kong HI, Crichton JE, Manthorpe JM. ChemInform Abstract: Stereoselective Synthesis of Ambiphilic Alkenes via Regioselective Methylation of α-Trifluoromethanesulfonyl Carbonyl Compounds with Trimethylsilyldiazomethane. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201143081 |
0.358 |
|
| 2009 |
Szpilman AM, Cereghetti DM, Manthorpe JM, Wurtz NR, Carreira EM. Synthesis and biophysical studies on 35-deoxy amphotericin B methyl ester. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 7117-28. PMID 19544513 DOI: 10.1002/Chem.200900231 |
0.726 |
|
| 2008 |
Szpilman AM, Cereghetti DM, Wurtz NR, Manthorpe JM, Carreira EM. Synthesis of 35-deoxy amphotericin B methyl ester: a strategy for molecular editing. Angewandte Chemie (International Ed. in English). 47: 4335-8. PMID 18454441 DOI: 10.1002/Anie.200800589 |
0.73 |
|
| 2008 |
Szpilman AM, Manthorpe JM, Carreira EM. Synthesis and biological studies of 35-deoxy amphotericin B methyl ester. Angewandte Chemie (International Ed. in English). 47: 4339-42. PMID 18442156 DOI: 10.1002/Anie.200800590 |
0.727 |
|
| 2008 |
Szpilman AM, Manthorpe JM, Carreira EM. Synthesis of 35-Deoxy Amphotericin B Methyl Ester Synfacts. 2008: 1245-1245. DOI: 10.1055/S-0028-1087282 |
0.73 |
|
| 2006 |
Arpin A, Manthorpe JM, Gleason JL. A practical chiral bicyclic thioglycolate lactam auxiliary for stereoselective quaternary carbon formation. Organic Letters. 8: 1359-62. PMID 16562891 DOI: 10.1021/Ol060106K |
0.661 |
|
| 2005 |
Manthorpe JM, Szpilman AM, Carreira EM. Scalable synthesis of a mycosamine donor. Overcoming difficult reactivity in allose systems Synthesis. 3380-3388. DOI: 10.1055/S-2005-918474 |
0.695 |
|
| 2002 |
Manthorpe JM, Gleason JL. Stereoselective formation of quaternary carbon centers: alkylation of alpha,alpha-disubstituted amide enolates. Angewandte Chemie (International Ed. in English). 41: 2338-41. PMID 12203585 DOI: 10.1002/1521-3773(20020703)41:13<2338::Aid-Anie2338>3.0.Co;2-M |
0.589 |
|
| 2002 |
Lange GL, Humber CC, Manthorpe JM. [2+2] Photoadditions with chiral 2,5-cyclohexadienone synthons Tetrahedron Asymmetry. 13: 1355-1362. DOI: 10.1016/S0957-4166(02)00339-7 |
0.62 |
|
| 2001 |
Manthorpe JM, Gleason JL. Stereoselective generation of E- and Z-disubstituted amide enolates. Reductive enolate formation from bicyclic thioglycolate lactams. Journal of the American Chemical Society. 123: 2091-2. PMID 11456846 DOI: 10.1021/Ja0058280 |
0.617 |
|
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