Controlling Regioselectivity in the Enantioselective N‐Alkylation of Indole Analogues Catalyzed by Dinuclear Zinc‐ProPhenol-Reference-Cited by-同舟云学术

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Controlling Regioselectivity in the Enantioselective N‐Alkylation of Indole Analogues Catalyzed by Dinuclear Zinc‐ProPhenol

Published:2017-07-19 Issue:35 Volume:56 Page:10451-10456
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Trost Barry M.¹^ORCID,Gnanamani Elumalai¹^ORCID,Hung Chao‐I (Joey)¹

Affiliation:

1. Department of Chemistry Stanford University Stanford CA 94305-5080 USA

Funder

National Institutes of Health

National Science Foundation

Fulbright Association

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201705315

Reference58 articles.

1.

2. Biogenetically-Inspired Total Synthesis of Epidithiodiketopiperazines and Related Alkaloids

3. Stereoselective manipulation of acetals derived from o-substituted benzaldehyde chromium tricarbonyl complexes

4. α-Amido Sulfones as Stable Precursors of Reactive N-Acylimino Derivatives

5. Cyclizations of N-Acyliminium Ions

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3. Direct Catalytic Asymmetric and Regiodivergent N1‐ and C3‐Allenylic Alkylation of Indoles;Angewandte Chemie;2023-04-13

4. Synthesis ofN-β-aminoacrylate substituted indolesvia^tBuOK catalyzed addition of indoles to ketenimines;Organic Chemistry Frontiers;2023

5. Chiral Phosphoric Acid‐Catalyzed Chemo‐ and Enantioselective N‐Alkylation of Indoles with Imines;Advanced Synthesis & Catalysis;2022-11-16

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