Mild and Efficient Pentafluorophenylammonium Triflate (PFPAT)-Catalyzed C-Acylations of Enol Silyl Ethers or Ketene Silyl (Thio)Acetals with Acid Chlorides-Reference-Cited by-同舟云学术

Mild and Efficient Pentafluorophenylammonium Triflate (PFPAT)-Catalyzed C-Acylations of Enol Silyl Ethers or Ketene Silyl (Thio)Acetals with Acid Chlorides

Published:2007-04-13 Issue:10 Volume:9 Page:1859-1862
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Iida Akira¹,Osada Jun¹,Nagase Ryohei¹,Misaki Tomonori¹,Tanabe Yoo¹

Affiliation:

1. Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo 669-1337, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol070191b

Reference69 articles.

1. (b) Vollhardt, K. P. C.; Schore, N. E.Organic Chemistry, 3rd ed.; Freeman: New York, 1999; p 1039.

2. (c) Clayden, J.; Greeves, N.; Warren, S.; Wothers, P.OrganicChemistry; Oxford: New York, 2001; p 726.

3. (d) Kürti, L.; Czakó, B.StrategicApplications of Named Reactions in Organic Synthesis; Elsevier: Burlington, 2005; p 86 and p 138.

4. Improvement of Boron Fluoride Method of Acylation of Ketones to Form β-Diketones. Ring Opening of 2-Acyl Cyclic Ketones to Form Keto Acids1

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