Howard E. Morton

Affiliations: 
AbbVie 
Area:
Organic Chemistry
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"Howard Morton"
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Dhaon MK, Zhou CC, Chemburkar S, et al. (2007) Synthesis, isolation, and characterization of ABT-578 equilibrium isomers Tetrahedron Letters. 48: 1059-1062
Kerdesky FAJ, Leanna MR, Zhang J, et al. (2006) An efficient multikilogram synthesis of ABT-963: A selective COX-2 inhibitor Organic Process Research and Development. 10: 512-517
Zhang J, Morton HE, Ji J. (2006) Confirmation and prevention of halogen exchange: practical and highly efficient one-pot synthesis of dibromo- and dichloropyridazinones Tetrahedron Letters. 47: 8733-8735
Ku YY, Grieme T, Raje P, et al. (2003) A practical and scaleable synthesis of A-224817.0, a novel nonsteroidal ligand for the glucocorticoid receptor. The Journal of Organic Chemistry. 68: 3238-40
Barnes DM, Ji J, Fickes MG, et al. (2002) Development of a catalytic enantioselective conjugate addition of 1,3-dicarbonyl compounds to nitroalkenes for the synthesis of endothelin-A antagonist ABT-546. Scope, mechanism, and further application to the synthesis of the antidepressant rolipram. Journal of the American Chemical Society. 124: 13097-105
Ku YY, Grieme T, Raje P, et al. (2002) Asymmetric synthesis of A-240610.0 via a new atropselective approach for axially chiral biaryls with chirality transfer. Journal of the American Chemical Society. 124: 4282-6
Kerdesky FAJ, Premchandran R, Wayne GS, et al. (2002) Synthesis of 2′-O-benzoyl-3-keto-6-O-propargyl-11,12-carbamoyl erythromycin A Organic Process Research and Development. 6: 869-875
Barnes DM, Ji J, Zhang J, et al. (2002) Development of a catalytic, asymmetric michael addition in the synthesis of endothelin antagonist ABT-546 Acs Symposium Series. 817: 45-59
DeMattei JA, Leanna MR, Li W, et al. (2001) An efficient synthesis of the taxane-derived anticancer agent ABT-271. The Journal of Organic Chemistry. 66: 3330-7
Ku YY, Grieme T, Sharma P, et al. (2001) Use of lodoacetylene as a dipolarphile in the synthesis of 5-lodoisoxazole derivatives Organic Letters. 3: 4185-4187
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