Nickel(0)-Catalyzed [2 + 2 + 1] Carbonylative Cycloaddition of Imines and Alkynes or Norbornene Leading to γ-Lactams-Reference-Cited by-同舟云学术

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Nickel(0)-Catalyzed [2 + 2 + 1] Carbonylative Cycloaddition of Imines and Alkynes or Norbornene Leading to γ-Lactams

Published:2014-11-04 Issue:45 Volume:136 Page:15877-15880
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hoshimoto Yoichi¹²,Ohata Tomoya¹,Sasaoka Yukari¹,Ohashi Masato¹,Ogoshi Sensuke¹³

Affiliation:

1. Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan

2. Frontier Research Base for Global Young Researchers, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan

3. JST, ACT-C, Suita, Osaka 565-0871, Japan

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Japan Science and Technology Agency

Asahi Glass Foundation

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja509171a

Reference55 articles.

1. Applications of Transition Metal Catalysis in Drug Discovery and Development

2. Recent development in 2-pyrrolidinone-containing nootropics

3. Structure of oxazolomycin, a novel β-lactone antibiotic

4. Syntheses and Biological Evaluation of (+)-Lactacystin and Analogs

5. Salinosporamide A: A Highly Cytotoxic Proteasome Inhibitor from a Novel Microbial Source, a Marine Bacterium of the New Genus Salinospora

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