Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis (Q43883582)

27 November 2017

title

Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis (English)

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27 November 2017

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David W C MacMillan

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27 November 2017

Joel F Austin

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27 November 2017

language of work or name

English

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publication date

1 February 2002

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Journal of the American Chemical Society

27 November 2017

published in

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volume

124

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issue

7

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27 November 2017

page(s)

1172-1173

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The Palladium-Catalyzed Cross-Coupling Reactions of Organotin Reagents with Organic Electrophiles[New Synthetic Methods(58)]

27 November 2017

cites work

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017255C

New strategies in organic catalysis: the first enantioselective organocatalytic Friedel-Crafts alkylation

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017255C

Catalytic Asymmetric Friedel-Crafts Alkylation of β,γ-Unsaturated α-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017255C

Carbon−Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and Sulfides

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017255C

Novel 5-hydroxytryptamine (5-HT3) receptor antagonists. III. Pharmacological evaluations and molecular modeling studies of optically active 4,5,6,7-tetrahydro-1H-benzimidazole derivatives

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017255C

A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017255C

Identifiers

DOI

10.1021/JA017255C

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27 November 2017

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