Michael J Humora

发表

Discovery of BIIB068: A Selective, Potent, Reversible Bruton's Tyrosine Kinase Inhibitor as an Orally Efficacious Agent for Autoimmune Diseases.

S. Sheikh, T. Bohnert, P. Schroeder, 2020, Journal of medicinal chemistry.

Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632

Sushil K. Srivastava, M. Pudipeddi, Zhongmin Xu, 2002 .

Acceleration of Petasis reactions of salicylaldehyde derivatives with molecular sieves.

Tina Talreja, Xiangli Shi, Zhili Xin, 2012, The Journal of organic chemistry.

Efficient asymmetric synthesis of the vasopeptidase inhibitor BMS-189921.

Chien-Kuang Chen, Bo Zhang, E. Vawter, 2003, Organic letters.

Synthesis of 2,6-diacetonylpiperidine. X-ray diffraction analysis of its N-benzoyl derivative

T. Brennan, Michael J Humora, J. Quick, 1978 .

N2,N3-DI-TERT-BUTOXYCARBONYLSPERMIDINE. A SYNTHESIS OF THE AGLYCONE OF THE LL-BM123 ANTIBIOTICS

Michael J Humora, J. Quick, 1979 .

Synthesis and anti-MRSA Activity of Novel Cephalosporin Derivatives

R. Perrone, M. Pucci, S. Hoeft, 2000 .

Process Development and Large-Scale Synthesis of BTK Inhibitor BIIB068

S. Ferguson, D. Patience, M. Macphee, 2020 .

A Practical Synthesis of l-Valyl-pyrrolidine-(2R)-boronic Acid: Efficient Recycling of the Costly Chiral Auxiliary (+)-Pinanediol

Maxime C Soumeillant, P. Manchand, D. Kronenthal, 2002 .

Tyrosine kinase inhibitors pyrimidinyl

Xiangli Shi, Ross A. Miller, A. Thompson, 2013 .

Discovery of BIIB042, a Potent, Selective, and Orally Bioavailable γ-Secretase Modulator.

K. Rhodes, Lin Xu, Tina Talreja, 2011, ACS medicinal chemistry letters.