Oxidative Cyclization Based on Reversing the Polarity of Enol Ethers and Ketene Dithioacetals. Construction of a Tetrahydrofuran Ring and Application to the Synthesis of (+)-Nemorensic Acid-Reference-Cited by-同舟云学术

Oxidative Cyclization Based on Reversing the Polarity of Enol Ethers and Ketene Dithioacetals. Construction of a Tetrahydrofuran Ring and Application to the Synthesis of (+)-Nemorensic Acid

Published:2002-08-01 Issue:34 Volume:124 Page:10101-10111
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liu Bin¹,Duan Shengquan¹,Sutterer Angela C.¹,Moeller Kevin D.¹

Affiliation:

1. Contribution from the Department of Chemistry, Washington University, St. Louis, Missouri 63130

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja026739l

Reference29 articles.

1. Intramolecular anodic olefin coupling reactions: a useful method for carbon-carbon bond formation

2. Reversing the Polarity of Enol Ethers: An Anodic Route to Tetrahydrofuran and Tetrahydropyran Rings

3. Pyrrolizidine alkaloids. XX. Nemorensine, an alkaloid from Senecio nemorensis L.

4. Total synthesis of (.+-.)-nemorensic acid

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