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Chaozhong Cai

Showing results (1-10 of 14) with videos related to

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The Journal of Organic Chemistry|February 16, 2002
Regioselective and stereoselective nucleophilic ring opening reactions of a phenyl-substituted aziridine: enantioselective synthesis of beta-substituted tryptophan, cysteine, and serine derivativesChiyi Xiong, Wei Wang, Chaozhong Cai, et al.
The Journal of Organic Chemistry|July 17, 2004
Virtually complete control of simple and face diastereoselectivity in the Michael addition reactions between achiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: practical method for preparation of beta-substituted pyroglutamic acids and prolinesVadim A Soloshonok, Hisanori Ueki, Rohit Tiwari, et al.
Chemical Communications (Cambridge, England)|May 8, 2010
Direct dehydrative cross-coupling of tautomerizable heterocycles with alkynes via Pd/Cu-catalyzed phosphonium couplingFu-An Kang, James C Lanter, Chaozhong Cai, et al.
Journal of the American Chemical Society|October 27, 2005
Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivityVadim A Soloshonok, Chaozhong Cai, Takeshi Yamada, et al.
The Journal of Organic Chemistry|August 31, 2002
Stereoselective synthesis of dipeptide beta-turn mimetics: 7-benzyl and 8-phenyl substituted azabicyclo[4.3.0]nonane amino acid estersWei Wang, Jianqing Yang, Jinfa Ying, et al.
Bioorganic & Medicinal Chemistry Letters|November 28, 2012
Novel 2-aminooctahydrocyclopentalene-3a-carboxamides as potent CCR2 antagonistsChaozhong Cai, Fu-An Kang, Cuifen Hou, et al.
Bioorganic & Medicinal Chemistry Letters|February 18, 2006
Identification of potent phenyl imidazoles as opioid receptor agonistsHenry J Breslin, Chaozhong Cai, Tamara A Miskowski, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2013
Discovery and SAR of 5-aminooctahydrocyclopentapyrrole-3a-carboxamides as potent CCR2 antagonistsChaozhong Cai, Dave F McComsey, Cuifen Hou, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2011
Overcoming hERG activity in the discovery of a series of 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonistsXuqing Zhang, Heather Hufnagel, Thomas Markotan, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2012
Identification of a dual δ OR antagonist/μ OR agonist as a potential therapeutic for diarrhea-predominant Irritable Bowel Syndrome (IBS-d)Henry J Breslin, Craig J Diamond, Robert W Kavash, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
The Journal of Organic Chemistry|February 16, 2002
Regioselective and stereoselective nucleophilic ring opening reactions of a phenyl-substituted aziridine: enantioselective synthesis of beta-substituted tryptophan, cysteine, and serine derivativesChiyi Xiong, Wei Wang, Chaozhong Cai, et al.
The Journal of Organic Chemistry|July 17, 2004
Virtually complete control of simple and face diastereoselectivity in the Michael addition reactions between achiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: practical method for preparation of beta-substituted pyroglutamic acids and prolinesVadim A Soloshonok, Hisanori Ueki, Rohit Tiwari, et al.
Chemical Communications (Cambridge, England)|May 8, 2010
Direct dehydrative cross-coupling of tautomerizable heterocycles with alkynes via Pd/Cu-catalyzed phosphonium couplingFu-An Kang, James C Lanter, Chaozhong Cai, et al.
Journal of the American Chemical Society|October 27, 2005
Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivityVadim A Soloshonok, Chaozhong Cai, Takeshi Yamada, et al.
The Journal of Organic Chemistry|August 31, 2002
Stereoselective synthesis of dipeptide beta-turn mimetics: 7-benzyl and 8-phenyl substituted azabicyclo[4.3.0]nonane amino acid estersWei Wang, Jianqing Yang, Jinfa Ying, et al.
Bioorganic & Medicinal Chemistry Letters|November 28, 2012
Novel 2-aminooctahydrocyclopentalene-3a-carboxamides as potent CCR2 antagonistsChaozhong Cai, Fu-An Kang, Cuifen Hou, et al.
Bioorganic & Medicinal Chemistry Letters|February 18, 2006
Identification of potent phenyl imidazoles as opioid receptor agonistsHenry J Breslin, Chaozhong Cai, Tamara A Miskowski, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2013
Discovery and SAR of 5-aminooctahydrocyclopentapyrrole-3a-carboxamides as potent CCR2 antagonistsChaozhong Cai, Dave F McComsey, Cuifen Hou, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2011
Overcoming hERG activity in the discovery of a series of 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonistsXuqing Zhang, Heather Hufnagel, Thomas Markotan, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2012
Identification of a dual δ OR antagonist/μ OR agonist as a potential therapeutic for diarrhea-predominant Irritable Bowel Syndrome (IBS-d)Henry J Breslin, Craig J Diamond, Robert W Kavash, et al.
Pageof 2