Tandem Nucleophilic Addition/Oxy-2-azonia-Cope Rearrangement for the Formation of Homoallylic Amides and Lactams: Total Synthesis and Structural Verification of Motuporamine G-Reference-Cited by-同舟云学术

Tandem Nucleophilic Addition/Oxy-2-azonia-Cope Rearrangement for the Formation of Homoallylic Amides and Lactams: Total Synthesis and Structural Verification of Motuporamine G

Published:2012-12-03 Issue:49 Volume:134 Page:20009-20012
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhou Lijun¹²,Li Zhiming¹,Zou Yue²,Wang Quanrui¹,Sanhueza Italo A.³,Schoenebeck Franziska³,Goeke Andreas²

Affiliation:

1. Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, China

2. Givaudan Fragrances (Shanghai) Ltd, 298 Li Shi Zhen Road, Shanghai 201203, China

3. Laboratory for Organic Chemistry, ETH Zürich, Wolfgang-Pauli-Strasse 10, 8093 Zürich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja310002m

Reference48 articles.

1. Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides

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4. A Knowledge-Based Approach in Designing Combinatorial or Medicinal Chemistry Libraries for Drug Discovery. 1. A Qualitative and Quantitative Characterization of Known Drug Databases

5. Key green chemistry research areas—a perspective from pharmaceutical manufacturers

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