Year |
Citation |
Score |
2017 |
David TK, Prashanth NK, Rajendraswami M, Pallalu D, Castelhano AL, Kates MJ, Blobaum AL, Jones CK, Emmitte KA, Conn PJ, Lindsley CW. Development and kilogram-scale synthesis of mGlu5 negative allosteric modulator VU0424238 (auglurant) Tetrahedron Letters. 58: 3554-3558. DOI: 10.1016/J.Tetlet.2017.07.100 |
0.307 |
|
2009 |
Crimmins MT, Ellis JM, Emmitte KA, Haile PA, McDougall PJ, Parrish JD, Zuccarello JL. Enantioselective total synthesis of brevetoxin A: unified strategy for the B, E, G, and J subunits. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 9223-34. PMID 19650091 DOI: 10.1002/Chem.200900776 |
0.632 |
|
2009 |
Crimmins MT, Zuccarello JL, Ellis JM, McDougall PJ, Haile PA, Parrish JD, Emmitte KA. Total synthesis of brevetoxin A. Organic Letters. 11: 489-92. PMID 19099481 DOI: 10.1021/Ol802710U |
0.629 |
|
2008 |
Hornberger KR, Badiang JG, Salovich JM, Kuntz KW, Emmitte KA, Cheung M. Regioselective synthesis of benzimidazole thiophene inhibitors of polo-like kinase 1 Tetrahedron Letters. 49: 6348-6351. DOI: 10.1016/J.Tetlet.2008.08.077 |
0.456 |
|
2005 |
Crimmins MT, McDougall PJ, Emmitte KA. A convergent coupling strategy for the formation of polycyclic ethers: stereoselective synthesis of the BCDE fragment of brevetoxin A. Organic Letters. 7: 4033-6. PMID 16119960 DOI: 10.1021/Ol051543M |
0.677 |
|
2004 |
Crimmins MT, Diaz CJ, Emmitte KA. A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones Heterocycles. 62: 179-183. DOI: 10.3987/Com-03-S(P)33 |
0.652 |
|
2002 |
Crimmins MT, Emmitte KA, Choy AL. Ring closing metathesis for the formation of medium ring ethers: The total synthesis of (-)-isolaurallene Tetrahedron. 58: 1817-1834. DOI: 10.1016/S0040-4020(02)00040-6 |
0.739 |
|
2001 |
Crimmins MT, Emmitte KA. Asymmetric total synthesis of (-)-isolaurallene. Journal of the American Chemical Society. 123: 1533-4. PMID 11456742 DOI: 10.1021/Ja005892H |
0.673 |
|
2000 |
Crimmins MT, Emmitte KA, Katz JD. Diastereoselective alkylations of oxazolidinone glycolates: a useful extension of the Evans asymmetric alkylation. Organic Letters. 2: 2165-7. PMID 10891257 DOI: 10.1021/Ol006091M |
0.678 |
|
2000 |
Crimmins MT, Emmitte KA. An efficient strategy for the synthesis of α,α'-cis and trans- disubstituted medium ring ethers Synthesis. 899-903. DOI: 10.1055/S-2000-6268 |
0.687 |
|
1999 |
Crimmins MT, Emmitte KA. Total synthesis of (+)-laurencin: an asymmetric alkylation-ring-closing metathesis approach to medium ring ethers. Organic Letters. 1: 2029-32. PMID 10836060 DOI: 10.1021/Ol991201E |
0.747 |
|
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