Asymmetric Synthesis of β-Substituted γ-Lactams via Rhodium/Diene-Catalyzed 1,4-Additions: Application to the Synthesis of (R)-Baclofen and (R)-Rolipram-Reference-Cited by-同舟云学术

Asymmetric Synthesis of β-Substituted γ-Lactams via Rhodium/Diene-Catalyzed 1,4-Additions: Application to the Synthesis of (R)-Baclofen and (R)-Rolipram

Published:2011-01-19 Issue:4 Volume:13 Page:788-791
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shao Cheng¹,Yu Hong-Jie¹,Wu Nuo-Yi¹,Tian Ping¹,Wang Rui¹,Feng Chen-Guo¹,Lin Guo-Qiang¹

Affiliation:

1. Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China, and State Key Laboratory of Applied Organic Chemistry and Institute of Biochemistry and Molecular Biology, Lanzhou University, Lanzhou 730000, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol103054a

Reference42 articles.

1. Gamma-lactams—A novel scaffold for highly potent and selective α7 nicotinic acetylcholine receptor agonists

2. γ- and δ-Amino Acids: Synthetic Strategies and Relevant Applications

3. Stereoselective synthesis of γ-amino acids

4. Enantioselective Michael Addition of Nitromethane to α,β-Enones Catalyzed by Chiral Quaternary Ammonium Salts. A Simple Synthesis of (R)-Baclofen

5. Enantioselective synthesis of (R)-(−)-baclofen via Ru(II)–BINAP catalyzed asymmetric hydrogenation

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