Mild and Efficient Synthesis of (Z)-α-Chloroalkylidene-β-lactones via the PdCl2-Catalyzed Cyclocarbonylation of 2-Alkynols-Reference-Cited by-同舟云学术

Mild and Efficient Synthesis of (Z)-α-Chloroalkylidene-β-lactones via the PdCl2-Catalyzed Cyclocarbonylation of 2-Alkynols

Published:2003-10-17 Issue:23 Volume:5 Page:4429-4432
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ma Shengming¹,Wu Bin¹,Zhao Shimin¹

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0357245

Reference38 articles.

1. Highly Enantioselective Preparation of Multifunctionalized Propargylic Building Blocks

2. A Novel, Highly Enantioselective Ketone Alkynylation Reaction Mediated by Chiral Zinc Aminoalkoxides

3. Solid-Phase Synthesis of Substituted Alkynes Using the Nicholas Reaction

4. Atom-Efficient Assembly of 1,5-Oxygen-Bridged Medium-Sized Carbocycles by Sequential Combination of a Ru-Catalyzed Alkyne−Alkene Coupling and a Prins-Type Cyclization

5. Stereoselective Synthesis of a Family of Alternating Polyols from Six-Carbon Epoxyalkynol Modules

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