J. Ng

发表

Development of a Large-Scale Process for an HIV Protease Inhibitor

D. Mehrotra, Chin Liu, J. Ng, 1997 .

Use of enzyme penicillin acylase in selective amidation/amide hydrolysis to resolve ethyl 3-amino-4-pentynoate isomers.

J. Ng, J. Behling, B. Landis, 1999, Bioorganic & medicinal chemistry.

Short efficient synthesis of the α-L-fucosidase inhibitor, deoxyfuconojirimycin [1,5-dideoxy-1,5-imino-L-fucitol] from D-lyxonolactone

R. Mueller, J. Ng, J. Behling, 1989 .

A practical synthesis of an HIV protease inhibitor intermediate - diastereoselective epoxide formation from chiral α-aminoaldehydes

J. Ng, C. Przybyla, F. W. Muellner, 1995 .

Plant carbonic anhydrase. Hydrase activity and its reversible inhibition.

Y. Pocker, J. Ng, 1974, Biochemistry.

An efficient synthesis of the antisecretory prostaglandin enisoprost

J. Ng, J. Behling, K. Babiak, 1991 .

A practical synthesis of 2-((1H-pyrrolo[2,3-b]pyridine-4-yl)methylamino)-5- fluoronicotinic acid.

M. Martinelli, J. Ng, P. Reider, 2006, Journal of Organic Chemistry.

AROMATIC FLUORINATIONS SUITABLE FOR FLUORINE‐18 LABELING OF ESTROGENS

J. Katzenellenbogen, M. Kilbourn, J. Ng, 1981 .

Reactions of higher order cyanocuprates derived from 2-lithiated furans: scope, limitations, and synthetic utility

J. Ng, J. Behling, A. L. Campbell, 1988 .

Synthesis from D-lyxonolactone of 1,4-Dideoxy-1,4-imino-L-arabinitol, a glucosidase inhibitor with in vitro anti-viral activity

J. Ng, J. Behling, A. L. Campbell, 1993 .

Reactions of Higher Order Cyanocuprates Derived from 2-Lithiated Furans: Scope, Limitations, and Synthetic Utility.

J. Ng, J. Behling, A. L. Campbell, 1988 .

Synthesis of Cinacalcet congeners

J. Ng, Xin Wang, Ying Chen, 2004 .

In situ cuprate formation via transmetalation between vinylstannanes and higher order cyanocuprates

J. Ng, J. Behling, A. L. Campbell, 1988 .

The Evolution of a Commercially Feasible Prostaglandin Synthesis

P. Collins, J. Ng, J. Behling, 1996 .

Lipase-catalyzed irreversible transesterification using enol esters : resolution of prostaglandin synthons 4-hydroxy-2-alkyl-2-cyclopentenones and inversion of the 4S enantiomer to the 4R enantiomer

Chi‐Huey Wong, J. Ng, Yi Fong. Wang, 1990 .

An Improved Procedure for the Synthesis of Prostaglandin Analogues

P. Collins, V. Kalish, J. Ng, 1990 .

The synthesis of β-Hydroxy-(E)-vinylstannanes using an "in-situ" generated cuprate reagent derived from (E)-bis-(tributylstannyl)ethylene

J. Ng, J. Behling, A. L. Campbell, 1989 .

Epoxide Formation from Aldehydes and Ketones-A Modified Method for Preparing the Corey-Chaykovsky Reagents

J. Ng, 1990 .

Epoxide Formation from Aldehydes and Ketones. A Modified Method for Preparing the Corey-Chaykovsky Reagents.

J. Ng, 1990 .