Y. Zhong

发表

Novel IBX‐Mediated Processes for the Synthesis of Amino Sugars and Libraries Thereof

K. Nicolaou, P. Baran, Y. Zhong, 2000 .

Hongming Li, M. McLaughlin, Y. Zhong, 2016, Topics in Current Chemistry.

Unusual pyrimidine participation: efficient stereoselective synthesis of potent dual orexin receptor antagonist MK-6096.

K. Maloney, Jeffrey C. Moore, R. Reamer, 2014, Organic letters.

Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase Inhibitor.

L. Tan, E. Sherer, Hongming Li, 2018, The Journal of organic chemistry.

Development of a practical, asymmetric synthesis of the hepatitis C virus protease inhibitor MK-5172.

G. Beutner, G. Humphrey, S. Dreher, 2013, Organic letters.

A Concise and Atom-Economical Suzuki-Miyaura Coupling Reaction Using Unactivated Trialkyl- and Triarylboranes with Aryl Halides.

Cheng-yi Chen, Hongmei Li, Y. Zhong, 2015, Organic letters.

Development of practical syntheses of potent non-nucleoside reverse transcriptase inhibitors

Jeremy P. Scott, D. Tellers, I. Davies, 2009 .

Synthesis of antifungal glucan synthase inhibitors from enfumafungin.

R. Ball, M. McLaughlin, R. Reamer, 2012, The Journal of organic chemistry.

13C NMR-Based Approaches for Solving Challenging Stereochemical Problems.

M. Reibarkh, I. E. Ndukwe, G. Martin, 2019, Organic letters.

Highly Enantioselective Rhodium-Catalyzed Transfer Hydrogenation of Tetrasubstituted Olefins: Application toward the Synthesis of GPR40 Agonist MK-2305.

D. Gauthier, Heather Wang, Y. Zhong, 2022, Organic letters.

Development of a Commercial Manufacturing Route to 2-Fluoroadenine, The Key Unnatural Nucleobase of Islatravir

Danielle M. Schultz, E. Sirota, J. McMullen, 2020 .

Total Synthesis of the CP Molecules CP-225,917 and CP-263,114- Part 2: Evolution of the Final Strategy.

Won Hyung Yoon, K. Nicolaou, P. Baran, 1999, Angewandte Chemie.

Iodine(V) reagents in organic synthesis. Part 3. New routes to heterocyclic compounds via o-iodoxybenzoic acid-mediated cyclizations: generality, scope, and mechanism.

K. Nicolaou, S. Barluenga, P. Baran, 2002, Journal of the American Chemical Society.

Mechanistic Studies of Periodinane-Mediated Reactions of Anilides and Related Systems.

K. Nicolaou, P. Baran, K. Sugita, 2001, Angewandte Chemie.

Iodine(V) reagents in organic synthesis. Part 2. Access to complex molecular architectures via Dess-Martin periodinane-generated o-imidoquinones.

K. Nicolaou, P. Baran, K. Sugita, 2002, Journal of the American Chemical Society.

Iodine(V) reagents in organic synthesis. Part 4. o-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes.

K. Nicolaou, P. Baran, Y. Zhong, 2002, Journal of the American Chemical Society.

Iodine(V) reagents in organic synthesis. Part 1. Synthesis of polycyclic heterocycles via Dess-Martin periodinane-mediated cascade cyclization: generality, scope, and mechanism of the reaction.

K. Nicolaou, P. Baran, K. Sugita, 2002, Journal of the American Chemical Society.

Synthesis of the GPR40 Partial Agonist MK-8666 through a Kinetically Controlled Dynamic Enzymatic Ketone Reduction.

Nicholas J Agard, L. Tan, Eric Ashley, 2016, Organic letters.

General Principles and Strategies for Salting-Out Informed by the Hofmeister Series

S. L. Zultanski, Y. Zhong, Feng Peng, 2017 .

A polar radical pair pathway to assemble the pyrimidinone core of the HIV integrase inhibitor raltegravir potassium.

K. Houk, R. Reamer, Gavin O. Jones, 2008, Angewandte Chemie.

Discovery and Process Development of MK‐4965, a Potent Nonnucleoside Reverse Transcriptase Inhibitor

T. Tucker, Y. Zhong, Jingjun Yin, 2012 .

An efficient access to 3,6-disubstituted 1H-pyrazolo[3,4-b]pyridines via a one-pot double SNAr reaction and pyrazole formation

Y. Zhong, N. Yasuda, Matthew G. Lindale, 2009 .

Efficient synthesis of functionalized pyrimidones via microwave-accelerated rearrangement reaction

Hua Zhou, D. Gauthier, Y. Zhong, 2006 .

Scalable Asymmetric Synthesis of MK-8998, a T-Type Calcium Channel Antagonist.

L. Tan, Jeffrey C. Moore, J. Janey, 2021, The Journal of organic chemistry.

Total synthesis of the CP-molecules (CP-263,114 and CP-225,917, phomoidrides B and A). 2. Model studies for the construction of key structural elements and first-generation strategy.

K. Nicolaou, P. Baran, Y. Zhong, 2002, Journal of the American Chemical Society.

An efficient synthesis of 4-chromanones

D. Gauthier, Y. Zhong, D. Askin, 2011 .

Total synthesis of the CP-molecules (CP-263,114 and CP-225,917, phomoidrides B and A). 3. Completion and synthesis of advanced analogues.

Won Hyung Yoon, K. Nicolaou, P. Baran, 2002, Journal of the American Chemical Society.

The Absolute Configuration and Asymmetric Total Synthesis of the CP Molecules (CP-263,114 and CP-225,917, Phomoidrides B and A)

Won Hyung Yoon, K. Nicolaou, P. Baran, 2000 .

Two New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoides

Y. Zhong, Jingyu. Su, L. Zeng, 1993 .

Efficient and Facile Glycol Cleavage Oxidation Using Improved Silica Gel-Supported Sodium Metaperiodate.

Y. Zhong, T. Shing, 1997, The Journal of organic chemistry.

Biomimetic Total Synthesis of Bisorbicillinol, Bisorbibutenolide, Trichodimerol, and Designed Analogues of the Bisorbicillinoids

Veroniki P. Vidali, K. Nicolaou, P. Baran, 2000 .

New Method for the Synthesis of Diversely Functionalized Imidazoles from N-Acylated α-Aminonitriles

R. Reamer, Y. Zhong, D. Askin, 2004 .

Selective oxidation at carbon adjacent to aromatic systems with IBX.

K. Nicolaou, P. Baran, Y. Zhong, 2001, Journal of the American Chemical Society.

Ring-selective synthesis of O-heterocycles from acyclic 3-O-allyl-monosaccharides via intramolecular nitrone–alkene cycloaddition

Y. Zhong, T. Shing, 2001 .

Scalable Synthesis of Diazeniumdiolates: Application to the Preparation of MK-8150.

Daniel J. Muzzio, K. Maloney, G. Humphrey, 2019, Organic letters.

Asymmetric Synthesis of Functionalized trans-Cyclopropoxy Building Block for Grazoprevir.

Rebecca T. Ruck, M. Truppo, Hongming Li, 2017, Organic letters.

Practical and efficient synthesis of N-halo compounds

Hua Zhou, R. Volante, D. Gauthier, 2005 .

Total Synthesis of the CP‐Molecules (CP‐263,114 and CP‐225,917, Phomoidrides B and A). Part 2. Model Studies for the Construction of Key Structural Elements and First‐Generation Strategy.

K. Nicolaou, P. Baran, Y. Zhong, 2002 .

Novel chemistry of alpha-tosyloxy ketones: applications to the solution- and solid-phase synthesis of privileged heterocycle and enediyne libraries.

K. Nicolaou, P. Baran, T. Ulven, 2002, Journal of the American Chemical Society.

New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B.

K. Nicolaou, P. Baran, K. Sugita, 2001, Angewandte Chemie.

Acyclic Stereodifferentiation: Selective Construction of Tetrahydropyran/Oxepane via Intramolecular Nitrone-Alkene Cycloaddition of Acyclic 3-O-Allylmonosaccharides.

F. Xue, Y. Zhong, T. Mak, 1998, The Journal of organic chemistry.

Clavudiol A and clavirolide A, two marine dolabellane diterpenes from the soft coral Clavularia viridis

J. Snyder, Y. Zhong, Jingyu. Su, 1991 .

Practical and cost-effective manufacturing route for the synthesis of a β-lactamase inhibitor.

Steven P. Miller, Y. Zhong, N. Yasuda, 2014, Organic letters.

A Practical and Scalable Synthesis of N‐Halo Compounds: 2‐Chloro‐6,7‐Dimethoxy‐1,2,3,4‐Tetrahydroisoquinoline

Y. Zhong, P. Bulger, 2011 .

Total synthesis of the CP-molecules (CP-263,114 and CP-225,917, phomoidrides B and A). 1. Racemic and asymmetric synthesis of bicyclo[4.3.1] key building blocks.

Won Hyung Yoon, K. Nicolaou, P. Baran, 2002, Journal of the American Chemical Society.

Biologically Active Metabolites from Marine Organisms

Xiong Fu, Y. Zhong, Jingyu. Su, 1995 .

Total Synthesis of the CP Molecules CP-263,114 and CP-225,917- Part 1: Synthesis of Key Intermediates and Intelligence Gathering.

Yun He, K C Nicolaou, Phil S Baran, 1999, Angewandte Chemie.

Development of a Scalable and Safer Synthesis of Diazeniumdiolates

Daniel J. Muzzio, K. Maloney, G. Humphrey, 2020 .

Practical synthesis of sultams via sulfonamide dianion alkylation: application to the synthesis of chiral sultams.

R. Reamer, Y. Zhong, D. Askin, 2003, Organic letters.

Rapid Access to Complex Molecular Architectures via o-Azaquinones.

K. Nicolaou, P. Baran, Y. Zhong, 2001, Angewandte Chemie.

New synthetic technology for the synthesis of hindered alpha-diazoketones via acyl mesylates.

Won Hyung Yoon, K. Nicolaou, P. Baran, 1999, Organic letters.

Novel strategies to construct the gamma-hydroxy lactone moiety of the CP molecules. Synthesis of the CP-225,917 core skeleton.

Won Hyung Yoon, K. Nicolaou, P. Baran, 1999, Organic letters.

A Novel Route to the Fused Maleic Anhydride Moiety of CP Molecules.

Won Hyung Yoon, K. Nicolaou, P. Baran, 1999, Angewandte Chemie.

Structure of a new sterol from the south china sponge Dysidea fragilis

Y. Zhong, Jingyu. Su, L. Zeng, 2010 .

Development of a Second-Generation, Highly Efficient Manufacturing Route for the HIV Integrase Inhibitor Raltegravir Potassium

Yong-Li Zhong, Guy R. Humphrey, Kevin M. Belyk, 2011 .

Terpenoids from Laurencia karlae

Y. Zhong, Jingyu. Su, L. Zeng, 1995 .

Novel Solution- and Solid-Phase Chemistry of α-Sulfonated Ketones Applicable to Combinatorial Chemistry

K. Nicolaou, Y. Zhong, A. Baran, 2000 .

Catalytic asymmetric synthesis of an HIV integrase inhibitor.

Hua Zhou, Yong-kui Sun, R. Reamer, 2009, Organic letters.

Directed Evolution to Reverse Epoxide Hydrolase Enantioselectivity for meso‐3,4‐Epoxytetrahydrofuran

Michael J. Ardolino, K. Hiraga, T. Itoh, 2023, ChemCatChem.

Calcium Dialkylamine Diazeniumdiolates: Synthesis, Stability, and Nitric Oxide Generation.

Amjad Ali, M. M. Lo, Y. Zhong, 2020, The Journal of organic chemistry.

Three New Diketopiperazines from a Marine Sponge Dysidea fragilis

Y. Zhong, T. Mak, L. Zeng, 1993 .

Two furano-sesquiterpenes from the South China Sea Sponge Dysidea fragilis

Y. Zhong, L. Zeng, K. Ma, 2010 .

Total synthesis of the CP-molecules (CP-263,114 and CP-225,917, phomoidrides B and A). 2. Model studies for the construction of key structural elements and first-generation strategy.

K. Nicolaou, P. Baran, Y. Zhong, 2002, Journal of the American Chemical Society.

A Concise and Atom-Economical Suzuki-Miyaura Coupling Reaction Using Unactivated Trialkyl- and Triarylboranes with Aryl Halides.

Cheng-yi Chen, Hongmei Li, Y. Zhong, 2015, Organic Letters.