Chaozhong Cai - Concepedia

Concepedia

Author

Chaozhong Cai

University of Arizona

Also Known As

Cai, Cai, Chaozhong, Chaozhong Cai

55

Publications

1.4K

Citations

20

H-Index

19

Concepts

All Affiliations

University of Arizona University of Oklahoma Springhouse Johnson & Johnson (United States)Janssen (United States)

CC

About

Chaozhong Cai is an author at University of Arizona specializing in organic chemistry, pharmacology, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	7	7	384
2	Engineering	6	6	370
3	Biochemistry	6	6	327
4	Biomolecular Engineering	6	6	370
5	Medicine	5	5	168

Chaozhong Cai

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24

Publications

1.4K

Citations

20

H-Index

	Year	Citations
Asymmetric synthesis of novel highly sterically constrained (2S,3S)-3-methyl-3-trifluoromethyl- and (2S,3S,4R)-3-trifluoromethyl-4-methylpyroglutamic acids Vadim A. Soloshonok, Chaozhong Cai, Victor J. Hruby, Tetrahedron EngineeringAsymmetric SynthesisFluorous SynthesisOrganic ChemistryChemistry	1999	105
(<i>S</i>)- or (<i>R</i>)-3-(<i>E</i>-Enoyl)-4-phenyl-1,3- oxazolidin-2-ones: Ideal Michael Acceptors To Afford a Virtually Complete Control of Simple and Face Diastereoselectivity in Addition Reactions with Glycine Derivatives Vadim A. Soloshonok, Chaozhong Cai, Victor J. Hruby Organic Letters	2000	87
Stereochemically defined C-substituted glutamic acids and their derivatives. 1. An efficient asymmetric synthesis of (2S,3S)-3-methyl- and -3-trifluoromethylpyroglutamic acids Vadim A. Soloshonok, Chaozhong Cai, Victor J. Hruby, Tetrahedron DerivativesBioorganic ChemistryBiochemistryEngineeringNatural Sciences	1999	86
Michael Addition Reactions between Chiral Equivalents of a Nucleophilic Glycine and (<i>S</i>)- or (<i>R</i>)-3-[(<i>E</i>)-Enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a General Method for Efficient Preparation of β-Substituted Pyroglutamic Acids. Case of Topographically Controlled Stereoselectivity Vadim A. Soloshonok, Chaozhong Cai, Takeshi Yamada, Journal of the American Chemical Society	2005	86
Virtually Complete Control of Simple and Face Diastereoselectivity in the Michael Addition Reactions between Achiral Equivalents of a Nucleophilic Glycine and (<i>S</i>)- or (<i>R</i>)-3-(<i>E</i>-Enoyl)-4-phenyl-1,3-oxazolidin-2-ones: Practical Method for Preparation of β-Substituted Pyroglutamic Acids and Prolines Vadim A. Soloshonok, Hisanori Ueki, Rohit Tiwari, The Journal of Organic Chemistry	2004	86
Rational Design of Highly Diastereoselective, Organic Base-Catalyzed, Room-Temperature Michael Addition Reactions<sup>1</sup> Vadim A. Soloshonok, Chaozhong Cai, Victor J. Hruby, The Journal of Organic Chemistry	2000	79
Michael Addition Reactions between Chiral Ni(II) Complex of Glycine and 3-(<i>trans</i>-Enoyl)oxazolidin-2-ones. A Case of Electron Donor−Acceptor Attractive Interaction-Controlled Face Diastereoselectivity<sup>1</sup> Chaozhong Cai, Vadim A. Soloshonok, Victor J. Hruby The Journal of Organic Chemistry	2001	78
Toward design of a practical methodology for stereocontrolled synthesis of χ-constrained pyroglutamic acids and related compounds. Virtually complete control of simple diastereoselectivity in the Michael addition reactions of glycine Ni(II) complexes with N-(enoyl)oxazolidinones Vadim A. Soloshonok, Chaozhong Cai, Victor J. Hruby Tetrahedron Letters Asymmetric CatalysisEngineeringNatural SciencesDiversity-oriented Synthesisχ-Constrained Pyroglutamic Acids	2000	75
Regioselective and Stereoselective Nucleophilic Ring Opening Reactions of A Phenyl-Substituted Aziridine: Enantioselective Synthesis of β-Substituted Tryptophan, Cysteine, and Serine Derivatives Chiyi Xiong, Wei Wang, Chaozhong Cai, The Journal of Organic Chemistry	2002	74
A Practical Asymmetric Synthesis of Enantiomerically Pure 3-Substituted Pyroglutamic Acids and Related Compounds Vadim A. Soloshonok, Chaozhong Cai, Victor J. Hruby Angewandte Chemie International Edition Room TemperatureSchiff BaseBiochemistryGlycine 1Natural Sciences	2000	71

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