Palladium‐Catalyzed Asymmetric Allylic Alkylations with Toluene Derivatives as Pronucleophiles-Reference-Cited by-同舟云学术

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Palladium‐Catalyzed Asymmetric Allylic Alkylations with Toluene Derivatives as Pronucleophiles

Published:2016-01-12 Issue:7 Volume:128 Page:2572-2576
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Mao Jianyou¹²,Zhang Jiadi²,Jiang Hui¹²,Bellomo Ana²,Zhang Mengnan²,Gao Zidong¹,Dreher Spencer D.³,Walsh Patrick J.²

Affiliation:

1. Department of Applied Chemistry China Agricultural University 2 West Yuanmingyuan Road Beijing 100193 P. R. China

2. Roy and Diana Vagelos Laboratories Department of Chemistry University of Pennsylvania 231 South 34th Street Philadelphia PA 19104-6323 USA

3. Department of Process Chemistry Merck Research Laboratories P.O. Box 2000 Rahway NJ 07065 USA

Funder

National Science Foundation

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201509917

Reference60 articles.

1.

2. Asymmetric Transition Metal-Catalyzed Allylic Alkylations

3. Pd Asymmetric Allylic Alkylation (AAA). A Powerful Synthetic Tool.

4. Pd-Catalyzed Enantioselective Allylic Substitution: New Strategic Options for the Total Synthesis of Natural Products

5. Pd-katalysierte enantioselektive allylische Substitution: neue strategische Optionen für die Naturstoffsynthese

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