B. Zhong

发表

Structure-based design of a new class of highly selective aminoimidazo[1,2-a]pyridine-based inhibitors of cyclin dependent kinases.

S. A. Watkins, D. Robertson, C. Hamdouchi, 2005, Bioorganic & medicinal chemistry letters.

Europium-labeled melanin-concentrating hormone analogues: ligands for measuring binding to melanin-concentrating hormone receptors 1 and 2.

L. Slieker, B. Zhong, J. Morin, 2004, Analytical biochemistry.

Identification of the Active Site Cysteine in Bovine Liver Monoamine Oxidase B

B. Zhong, R. Silverman, 1997 .

Meeting the potential emergency global drug supply challenge of hydroxychloroquine for COVID-19

B. Zhong, Tony Y. Zhang, 2020, Medicine in Drug Discovery.

Uronium sulfate, [OHC(NH2)2]2(SO4)

B. Zhong, C. Stern, D. Ellis, 1999 .

Pharmacological profiles of an anticholinergic agent, phencynonate hydrochloride, and its optical isomers

B. Zhong, J. Ruan, Ke-liang Liu, 2005, Acta Pharmacologica Sinica.

Rearrangement of aromatic sulfonate anions in the gas phase

B. Zhong, M. Tevesz, W. Winnik, 1993 .

Negativeion, Chemical-Ionization Mass Spectrometry of Sulfonic Acid Esters of Carbohydrates

B. Zhong, M. Tevesz, W. Winnik, 1998 .

Synthesis and crystal structure of [CuL0.5(Ac)2]n⋅0.5nCHCl3 (L = 2,5-bis(4-pyridyl)-1,3,4-oxadiazole)

B. Zhong, Li-ping Liu, He Liu, 2004 .

An Improved Procedure for the Synthesis of Substituted -Hydroxynitriles

B. Zhong, R. Silverman, Joseph J. P. Zhou, 1998 .

Improved Procedure for the Synthesis of Substituted .beta.-Hydroxy Nitriles

B. Zhong, R. Silverman, Joseph J. P. Zhou, 1995 .

Syntheses of amino nitrones. Potential intramolecular traps for radical intermediates in monoamine oxidase-catalyzed reactions.

B. Zhong, R. Silverman, X. Lu, 1998, Bioorganic & medicinal chemistry.

Asymmetric synthesis of chiral organofluorine compounds: use of nonracemic fluoroiodoacetic acid as a practical electrophile and its application to the synthesis of monofluoro hydroxyethylene dipeptide isosteres within a novel series of HIV protease inhibitors.

B. Zhong, A. Myers, J. Barbay, 2001, Journal of the American Chemical Society.

Synthesis of highly epimerizable N-protected α-amino aldehydes of high enantiomeric excess

B. Zhong, A. Myers, D. Kung, 2000 .

Optical Resolution, Stereoselective Synthesis, and Crystal Structure of 9α‐(3‐Azabicyclo[3,3,1]nonanyl)‐2′‐cyclopentyl‐2′‐hydroxy‐2′‐phenylacetate

B. Zhong, Yu-lin Deng, Ke-liang Liu, 2005 .

Observations Concerning the Existence and Reactivity of Free α-Amino Aldehydes as Chemical Intermediates: Evidence for Epimerization-Free Adduct Formation with Various Nucleophiles

B. Zhong, A. Myers, Andrew Kung, 2000 .

Study on Synthesis of Thebaine Derivatives

B. Zhong, Bo Wu, Z. Gong, 2005 .

Synthesis and Crystal Structure of 17-Allyl-4,5-anhydro-7α-[( R )-1-hydroxy-1-methyl-3-(2-thienyl)propyl]-6-methoxy-6,14-ethanomorphinan-3,4,5-triol

B. Zhong, He Liu, Jing-Yi Wang, 2005 .

Crystal Structure of Monoaquobis (1,10-phenanthroline)nickel(II) Chloride

B. Zhong, Li-ping Liu, Li-Ping Liu, 2004 .

Synthesis of N‐Aryl‐2‐substituted Tetrahydrobenzimidazoles via Direct N‐Arylation

B. Zhong, He Liu, Mei Li, 2007 .

Enantiospecific Synthesis of Penehyclidine Hydrochloride and Its Piperidine Derivatives with R Configuration

B. Zhong, Bo Wu, Ke-liang Liu, 2006 .

Synthesis of the optical isomers of a new anticholinergic drug, penehyclidine hydrochloride (8018).

B. Zhong, Bo Wu, Ke-liang Liu, 2005, Bioorganic & medicinal chemistry letters.

Stereoselective Synthesis of the Optical Isomers of a New Muscarinic Receptor Antagonist, HL‐031120

B. Zhong, Ke-liang Liu, He Liu, 2006 .

Studies on crystal structure of inclusion chiral crystal of (S)-α-cyclopentyl-α-hydroxyl-α-thienylacetic acid with (R)-α-methyl benylamine

B. Zhong, Ke-liang Liu, Chun-He Liu, 2004 .

Crystal Structure of (2S,5R)-2-(tert-Butyl)-5-phenyl-5-(cyclopentyl-1-ol)-1,3-dioxolan-4-one

B. Zhong, Ke-liang Liu, Chun-He Liu, 2004 .

Stereoselective Synthesis of α-Alkyl-α-Hydroxylphenylacetic Acid Part (I): Asymmetric Alkylation of (S)-Mandelic Acid

B. Zhong, Bo Wu, Ke-liang Liu, 2004 .

Synthesis and crystal structure of quinuclidin-3-yl 2-cyclopentyl-2-hydroxy-2-phenylacetate

B. Zhong, Bo Wu, Ke-liang Liu, 2005 .

Comparative study on pharmacological effects of DM-phencynonate hydrochloride and its optical isomers

B. Zhong, J. Ruan, Ke-liang Liu, 2005, Acta Pharmacologica Sinica.

Synthesis and Crystal Structure of (9s)-N-methyl-3-azabicyclo[3.3.1] nonan-9-yl (cyclopentyl)(hydroxy)(2-thienyl)Acetate Hydrochloride

B. Zhong, Yu-lin Deng, Ke-liang Liu, 2005 .

Stereoselective Synthesis of 3-azabicyclo[3,3,1]Nonan-9α-yl α-(cyclopentyl-1-ene)-α-hydroxy-α-phenylacetate Hydrochloride

B. Zhong, Ke-liang Liu, He Liu, 2005 .

Stereoselective Synthesis of the Optical Isomers of a New Muscarinic Receptor Antagonist, HL-031120.

B. Zhong, Ke-liang Liu, He Liu, 2006 .

Stereoselective Synthesis of α‐Alkyl‐α‐hydroxyphenylacetic Acid. Part 1. Asymmetric Alkylation of (S)‐Mandelic Acid.

B. Zhong, Bo Wu, Ke-liang Liu, 2005 .

Novel route to the synthesis of 4-quinolyl isothiocyanates

M. Vieth, C. Hamdouchi, R. Al-awar, 2006 .

Poly(ethylene glycol)-supported enzyme inactivators. Efficient identification of the site of covalent attachment to alpha-chymotrypsin by PEG-TPCK.

B. Zhong, R. Silverman, J. C. Woo, 2004, Bioconjugate chemistry.

Synthesis of C-Protected α-Amino Aldehydes of High Enantiomeric Excess from Highly Epimerizable N-Protected α-Amino Aldehydes

B. Zhong, A. Myers, D. Kung, 2000 .

LY2801653 is an orally bioavailable multi-kinase inhibitor with potent activity against MET, MST1R, and other oncoproteins, and displays anti-tumor activities in mouse xenograft models

J. Graff, R. Walgren, C. Shih, 2012, Investigational New Drugs.

Discovery of 2-arylamino-4-(1-methyl-3-isopropylsulfonyl-4-pyrazol-amino)pyrimidines as potent anaplastic lymphoma kinase (ALK) inhibitors.

B. Zhong, Gang-Ying Chen, Ruihao Zhang, 2015, Bioorganic & medicinal chemistry letters.

Abstract 2096: Bozitinib, a highly selective inhibitor of cMet, demonstrates robust activity in gastric, lung, hepatic and pancreatic in vivo models

B. Zhong, G. Choy, S. Redkar, 2017 .

Preparation of Chiral, C-Protected α-Amino Aldehydes of High Optical Purity and Their Use as Condensation Components in a Linear Synthesis Strategy

B. Zhong, A. Myers, D. Kung, 1999 .

Preparation of Chiral, C‐Protected α‐Amino Aldehydes of High Optical Purity and Their Use as Condensation Components in a Linear Synthesis Strategy.

B. Zhong, A. Myers, D. Kung, 2000 .

Synthesis and Characterization of Thienorphine and Its Glucuronide Conjugate

B. Zhong, Bo Wu, Z. Gong, 2005 .

Synthesis and Characterization of Thienorphine and Its Glucuronide Conjugate.

B. Zhong, Bo Wu, Z. Gong, 2005 .

Synthesis of 2H- and 3H-labeled N-cyclopropylmethyl-7α-[(R)-1-hydroxy-1-methyl-3-(2thienyl)-propyl]-6,14-endoethano-6,7,8,14-tetrahydro nororipavine

B. Zhong, Bo Wu, Chun-He Liu, 2005 .

Design and synthesis of novel 3-sulfonylpyrazol-4-amino pyrimidines as potent anaplastic lymphoma kinase (ALK) inhibitors.

B. Zhong, Gang-Ying Chen, Ruihao Zhang, 2016, Bioorganic & medicinal chemistry letters.