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Daniel Tzvi Cohen - Publications

Affiliations: 
2013- Chemistry Massachusetts Institute of Technology, Cambridge, MA, United States 
Website:
http://web.mit.edu/chemistry/buchwald/people/profiles-postdoc.html#cohen
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21 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Cohen DT, Zhang C, Fadzen CM, Mijalis AJ, Hie L, Johnson KD, Shriver Z, Plante O, Miller SJ, Buchwald SL, Pentelute BL. A chemoselective strategy for late-stage functionalization of complex small molecules with polypeptides and proteins. Nature Chemistry. PMID 30397320 DOI: 10.1038/S41557-018-0154-0  0.395
2017 Scheidt K, Hovey T, Cohen D, Walden D, Cheong P. A Carbene Catalysis Strategy for the Synthesis of Protoilludane Natural Products. Angewandte Chemie (International Ed. in English). PMID 28632913 DOI: 10.1002/Anie.201705308  0.601
2017 Wang MH, Barsoum D, Schwamb CB, Cohen DT, Goess BC, Riedrich M, Chan A, Maki BE, Mishra RK, Scheidt KA. Catalytic, Enantioselective β-Protonation through a Cooperative Activation Strategy. The Journal of Organic Chemistry. PMID 28441019 DOI: 10.1021/Acs.Joc.7B00334  0.767
2015 Cohen DT, Zhang C, Pentelute BL, Buchwald SL. An Umpolung Approach for the Chemoselective Arylation of Selenocysteine in Unprotected Peptides. Journal of the American Chemical Society. 137: 9784-7. PMID 26225900 DOI: 10.1021/Jacs.5B05447  0.475
2015 Wang MH, Cohen DT, Schwamb CB, Mishra RK, Scheidt KA. Enantioselective β-Protonation by a Cooperative Catalysis Strategy. Journal of the American Chemical Society. 137: 5891-4. PMID 25929160 DOI: 10.1055/S-0034-1381154  0.691
2015 Cohen DT, Johnston RC, Rosson NT, Cheong PH, Scheidt KA. Functionalized cyclopentenes through a tandem NHC-catalyzed dynamic kinetic resolution and ambient temperature decarboxylation: mechanistic insight and synthetic application. Chemical Communications (Cambridge, England). 51: 2690-3. PMID 25575249 DOI: 10.1039/C4Cc09308A  0.646
2015 Cohen DT, Buchwald SL. Mild palladium-catalyzed cyanation of (hetero)aryl halides and triflates in aqueous media. Organic Letters. 17: 202-5. PMID 25555140 DOI: 10.1021/Ol5032359  0.539
2015 Cohen DT, Zhang C, Pentelute BL, Buchwald SL. An Umpolung Approach for the Chemoselective Arylation of Selenocysteine in Unprotected Peptides Journal of the American Chemical Society. 137: 9784-9787. DOI: 10.1021/jacs.5b05447  0.335
2014 Johnston RC, Cohen DT, Eichman CC, Scheidt KA, Cheong PH. Catalytic Kinetic Resolution of a Dynamic Racemate: Highly Stereoselective β-Lactone Formation by N-Heterocyclic Carbene Catalysis. Chemical Science (Royal Society of Chemistry : 2010). 5: 1974-1982. PMID 25045464 DOI: 10.1039/C4Sc00317A  0.799
2013 Cohen DT, Eichman CC, Phillips EM, Zarefsky ER, Scheidt KA. Corrigendum: Catalytic Dynamic Kinetic Resolutions with N-Heterocyclic Carbenes: Asymmetric Synthesis of Highly Substituted β-Lactones Angewandte Chemie International Edition. 52: 5203-5203. DOI: 10.1002/Anie.201302333  0.809
2012 Cohen DT, Scheidt KA. Cooperative Lewis acid/N-heterocyclic carbene catalysis. Chemical Science (Royal Society of Chemistry : 2010). 3: 53-57. PMID 26413259 DOI: 10.1039/C1Sc00621E  0.67
2012 Izquierdo J, Hutson GE, Cohen DT, Scheidt KA. A continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis. Angewandte Chemie (International Ed. in English). 51: 11686-98. PMID 23074146 DOI: 10.1002/Anie.201203704  0.764
2012 Cohen DT, Eichman CC, Phillips EM, Zarefsky ER, Scheidt KA. Catalytic dynamic kinetic resolutions with N-heterocyclic carbenes: asymmetric synthesis of highly substituted β-lactones. Angewandte Chemie (International Ed. in English). 51: 7309-13. PMID 22700327 DOI: 10.1002/Anie.201203382  0.821
2012 Dugal-Tessier J, O'Bryan EA, Schroeder TB, Cohen DT, Scheidt KA. An N-heterocyclic carbene/Lewis acid strategy for the stereoselective synthesis of spirooxindole lactones. Angewandte Chemie (International Ed. in English). 51: 4963-7. PMID 22489096 DOI: 10.1002/Anie.201201643  0.82
2012 Cohen DT, Scheidt KA. Cooperative Lewis acid/N-heterocyclic carbene catalysis Chemical Science. 3: 53-57. DOI: 10.1039/c1sc00621e  0.587
2012 Izquierdo J, Hutson GE, Cohen DT, Scheidt KA. Anwendungen der Katalyse mit N-heterocyclischen Carbenen in Totalsynthesen Angewandte Chemie. 124: 11854-11866. DOI: 10.1002/Ange.201203704  0.711
2011 Cohen DT, Cardinal-David B, Scheidt KA. Lewis acid activated synthesis of highly substituted cyclopentanes by the N-heterocyclic carbene catalyzed addition of homoenolate equivalents to unsaturated ketoesters. Angewandte Chemie (International Ed. in English). 50: 1678-82. PMID 21308931 DOI: 10.1002/Anie.201005908  0.82
2011 Cohen DT, Cardinal-David B, Roberts JM, Sarjeant AA, Scheidt KA. NHC-catalyzed/titanium(IV)-mediated highly diastereo- and enantioselective dimerization of enals. Organic Letters. 13: 1068-71. PMID 21271734 DOI: 10.1021/Ol103112V  0.794
2011 Cohen DT, Cardinal-David B, Roberts JM, Sarjeant AA, Scheidt KA. Titanium-Mediated Diastereo- and Enantioselective Dimerizationof Enals Synfacts. 2011: 665-665. DOI: 10.1055/S-0030-1260366  0.777
2011 Cohen DT, Cardinal-David B, Scheidt KA. NHC-Catalyzed Addition of Homoenolate Equivalents to UnsaturatedKeto Esters Synfacts. 2011: 437-437. DOI: 10.1055/S-0030-1259613  0.806
2011 Cohen DT, Cardinal-David B, Scheidt KA. Innentitelbild: Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N-Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters (Angew. Chem. 7/2011) Angewandte Chemie. 123: 1484-1484. DOI: 10.1002/Ange.201007985  0.811
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