Year |
Citation |
Score |
2017 |
Olsen KL, Jensen MR, MacKay JA. A mild halogenation of pyrazoles using sodium halide salts and Oxone Tetrahedron Letters. 58: 4111-4114. DOI: 10.1016/J.Tetlet.2017.09.042 |
0.347 |
|
2014 |
Bhat V, Dave A, MacKay JA, Rawal VH. The Chemistry of Hapalindoles, Fischerindoles, Ambiguines, and Welwitindolinones. The Alkaloids. Chemistry and Biology. 73: 65-160. PMID 26521649 DOI: 10.1016/B978-0-12-411565-1.00002-0 |
0.618 |
|
2014 |
MacKay JA, Wetzel NR. Exploring the wittig reaction: A collaborative guided-inquiry experiment for the organic chemistry laboratory Journal of Chemical Education. 91: 722-725. DOI: 10.1021/Ed3003836 |
0.324 |
|
2014 |
Bhat V, Dave A, MacKay JA, Rawal VH. The Chemistry of Hapalindoles, Fischerindoles, Ambiguines, and Welwitindolinones Alkaloids: Chemistry and Biology. 73: 65-160. DOI: 10.1016/B978-0-12-411565-1.00002-0 |
0.62 |
|
2012 |
MacKay JA, Landis ZC, Motika SE, Kench MH. The intramolecular allenolate Rauhut-Currier reaction. The Journal of Organic Chemistry. 77: 7768-74. PMID 22866944 DOI: 10.1021/Jo3015769 |
0.37 |
|
2011 |
Bhat V, Mackay JA, Rawal VH. Lessons Learned while Traversing the Welwitindolinone Alkaloids Obstacle Course. Tetrahedron. 67: 100997-10104. PMID 22962500 DOI: 10.1016/J.Tet.2011.09.088 |
0.649 |
|
2011 |
Bhat V, Mackay JA, Rawal VH. Directed oxidative cyclizations to C2- or C4-positions of indole: efficient construction of the bicyclo[4.3.1]decane core of welwitindolinones. Organic Letters. 13: 3214-7. PMID 21615098 DOI: 10.1021/Ol201122F |
0.639 |
|
2010 |
Duffey TA, Mackay JA, Vedejs E. Catalytic parallel kinetic resolution under homogeneous conditions. The Journal of Organic Chemistry. 75: 4674-85. PMID 20557113 DOI: 10.1021/Jo100695Z |
0.685 |
|
2006 |
MacKay JA, Vedejs E. Synthesis and reactivity of new chiral bicyclic phospholanes as acyl-transfer catalysts. The Journal of Organic Chemistry. 71: 498-503. PMID 16408956 DOI: 10.1021/Jo0519155 |
0.521 |
|
2005 |
MacKay JA, Bishop RL, Rawal VH. Rapid synthesis of the N-methylwelwitindolinone skeleton. Organic Letters. 7: 3421-4. PMID 16048307 DOI: 10.1021/Ol051043T |
0.593 |
|
2004 |
MacKay JA, Vedejs E. Enantioselective acylation using a second-generation P-aryl-2-phosphabicyclo[3.3.0]octane catalyst. The Journal of Organic Chemistry. 69: 6934-7. PMID 15387630 DOI: 10.1021/Jo049112P |
0.52 |
|
2003 |
Vedejs E, Daugulis O, Harper LA, MacKay JA, Powell DR. A comparison of monocyclic and bicyclic phospholanes as acyl-transfer catalysts. The Journal of Organic Chemistry. 68: 5020-7. PMID 12816454 DOI: 10.1021/jo030007+ |
0.687 |
|
2001 |
Vedejs E, MacKay JA. Kinetic resolution of allylic alcohols using a chiral phosphine catalyst. Organic Letters. 3: 535-6. PMID 11178818 DOI: 10.1021/Ol006923G |
0.505 |
|
2001 |
Vedejs E, Daugulis O, MacKay JA, Rozners E. Enantioselective acyl transfer using chiral phosphine catalysts Synlett. 1499-1505. DOI: 10.1055/S-2001-17436 |
0.646 |
|
Show low-probability matches. |