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Literature DB >> 11317301

Modular Pyridinyl Peptide Ligands in Asymmetric Catalysis: Enantioselective Synthesis of Quaternary Carbon Atoms Through Copper-Catalyzed Allylic Substitutions This research was supported by the National Institutes of Health (GM47480 and GM57212). Additional funds were provided by DuPont.

Courtney A. Luchaco-Cullis¹, Hirotake Mizutani, Kerry E. Murphy, Amir H. Hoveyda.

Abstract

Entities: Chemical

Year: 2001 PMID： 11317301

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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12 in total

1. Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis.

Authors: Jiajie Feng; Michael Holmes; Michael J Krische
Journal: Chem Rev Date: 2017-09-14 Impact factor: 60.622

2. Chiral imine copper chloride-catalyzed enantioselective desymmetrization of 2-substituted 1,2,3-propanetriols.

Authors: Byunghyuck Jung; Sung Ho Kang
Journal: Proc Natl Acad Sci U S A Date: 2007-01-22 Impact factor: 11.205

3. Synthesis of quaternary carbon stereogenic centers through enantioselective Cu-catalyzed allylic substitutions with vinylaluminum reagents.

Authors: Fang Gao; Kevin P McGrath; Yunmi Lee; Amir H Hoveyda
Journal: J Am Chem Soc Date: 2010-10-13 Impact factor: 15.419

4. Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.

Authors: Douglas C Behenna; Justin T Mohr; Nathaniel H Sherden; Smaranda C Marinescu; Andrew M Harned; Kousuke Tani; Masaki Seto; Sandy Ma; Zoltán Novák; Michael R Krout; Ryan M McFadden; Jennifer L Roizen; John A Enquist; David E White; Samantha R Levine; Krastina V Petrova; Akihiko Iwashita; Scott C Virgil; Brian M Stoltz
Journal: Chemistry Date: 2011-11-14 Impact factor: 5.236

5. Quaternary carbon stereogenic centers through copper-catalyzed enantioselective allylic substitutions with readily accessible aryl- or heteroaryllithium reagents and aluminum chlorides.

Authors: Fang Gao; Yunmi Lee; Kyoko Mandai; Amir H Hoveyda
Journal: Angew Chem Int Ed Engl Date: 2010-11-02 Impact factor: 15.336

Modular Pyridinyl Peptide Ligands in Asymmetric Catalysis: Enantioselective Synthesis of Quaternary Carbon Atoms Through Copper-Catalyzed Allylic Substitutions This research was supported by the National Institutes of Health (GM47480 and GM57212). Additional funds were provided by DuPont.

1. Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis.

2. Chiral imine copper chloride-catalyzed enantioselective desymmetrization of 2-substituted 1,2,3-propanetriols.

3. Synthesis of quaternary carbon stereogenic centers through enantioselective Cu-catalyzed allylic substitutions with vinylaluminum reagents.

4. Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.

5. Quaternary carbon stereogenic centers through copper-catalyzed enantioselective allylic substitutions with readily accessible aryl- or heteroaryllithium reagents and aluminum chlorides.

6. Catalytic double stereoinduction in asymmetric allylic alkylation of oxindoles.

7. Catalytic asymmetric synthesis of all-carbon quaternary stereocenters.

Review 8. Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms.

9. Enantioselective construction of remote quaternary stereocentres.

10. Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes.