E. Moher

发表

Cryptophycins-309, 249 and other cryptophycin analogs: Preclinical efficacy studies with mouse and human tumors

Richard E. Moore, M. Martinelli, C. Shih, 2005, Investigational New Drugs.

Synthetic studies on quassinoids: total synthesis of (-)-chaparrinone, (-)-glaucarubolone, and (+)-glaucarubinone

J. Collins, R. Gross, P. Grieco, 1993 .

Synthetic studies on quassinoids: total synthesis of simalikalactone D and assignment of the absolute configuration of the .alpha.-methylbutyrate ester side chain.

J. Collins, P. Grieco, E. Moher, 1992 .

Catalytic Regioselective Sulfonylation of α-Chelatable Alcohols: Scope and Mechanistic Insight

M. Martinelli, J. M. Pawlak, R. Vaidyanathan, 2002 .

Process Development for a Key Synthetic Intermediate of LY2140023, a Clinical Candidate for the Treatment of Schizophrenia

Michael E. Laurila, Cheryl A. Bye, K. A. Sullivan, 2011 .

Preparation of (.mu.-H)3Os3(CO)9(.mu.3-C)(B5H8) and (.mu.3-H)3Os3(CO)9(.mu.3-C)(C2B10H11): "alkylation" of pentaborane(9) and 1,2-dicarbadodecaborane by a triosmium methylidyne cluster

J. Wermer, D. Jan, S. Shore, 1988 .

Dibutyltin Oxide Catalyzed Selective Sulfonylation of α-Chelatable Primary Alcohols

M. Martinelli, R. Vaidyanathan, N. Nayyar, 1999 .

Development and Manufacturing GMP Scale-Up of a Continuous Ir-Catalyzed Homogeneous Reductive Amination Reaction

Martin D. Johnson, A. McFarland, G. Lambertus, 2016 .

Synthesis of cryptophycin 52 using the Shi epoxidation.

M. Martinelli, B. Norman, D. W. Hoard, 2002, Organic letters.

Synthesis of cryptophycin 52 using the sharpless asymmetric dihydroxylation: diol to epoxide transformation optimized for a base-sensitive substrate.

R. Moore, D. W. Hoard, J. Liang, 2000, The Journal of organic chemistry.

Synthesis and biological evaluation of cryptophycin analogs with substitution at C-6 (fragment C region).

M. Martinelli, R. Schultz, C. Shih, 1999, Bioorganic & medicinal chemistry letters.

Synthesis of Unit A of Cryptophycin via a [2,3]-Wittig Rearrangement.

Richard E. Moore, M. Tius, M. Martinelli, 1999, The Journal of organic chemistry.

A quassinoid (peninsularinone) and a steroid from Castela peninsularis

J. Huffman, P. Grieco, Motohide Seya, 1994 .

Novel asymmetric synthesis of a bicyclo[3.1.0]hexane derivative by an efficient retro-diels-alder strategy

E. Moher, 1996 .

(2S,1'S,2'R,3'R)-2-(2'-Carboxy-3'-hydroxymethylcyclopropyl) glycine is a highly potent group 2 and 3 metabotropic glutamate receptor agonist with oral activity.

D. Schoepp, C. Pedregal, J. Pérez-Castells, 2004, Journal of medicinal chemistry.

Design, Development, and Scale-Up of a Selective meso-Epoxide Desymmetrization Process

David D. Anderson, Mindy B. Forst, Richard D. Miller, 2007 .

(R)-(+)- and (S)-(-)-5-Ethyl-5-methyl-1,3-dioxolane-2,4-dione reagents for the direct preparation of .alpha.-hydroxy-.alpha.-methylbutyrate esters: assignment of the absolute configuration of the .alpha.-acetoxy-.alpha.-methylbutyrate ester side chain of quassimarin via total synthesis

J. Collins, P. Grieco, E. Moher, 1993 .

TMG catalyzed cyclopropanation of cyclopentenone. Illustration by a simple synthesis of bicyclo[3.1.0]hexane-2-one derivatives

Tony Y. Zhang, Fuyao Zhang, E. Moher, 2007 .

Synthesis of Methyl 7,9-Dimethyl-5-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepine-1-carboxylate and Its Analogues

C. Hadden, Jeremy T. Spitler, C. Alt, 2014, Synthesis.