Ti-Crossed-Claisen Condensation between Carboxylic Esters and Acid Chlorides or Acids: A Highly Selective and General Method for the Preparation of Various β-Keto Esters-Reference-Cited by-同舟云学术

Ti-Crossed-Claisen Condensation between Carboxylic Esters and Acid Chlorides or Acids: A Highly Selective and General Method for the Preparation of Various β-Keto Esters

Published:2005-02-11 Issue:9 Volume:127 Page:2854-2855
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Misaki Tomonori¹,Nagase Ryohei¹,Matsumoto Kunshi¹,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

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja043833o

Reference31 articles.

1. Smith, M. B.; March, J.Advanced Organic Chemistry; Wiley: New York, 2001; p 569.

2. The Selective Claisen and Dieckmann Ester Condensations Promoted by Dichlorobis(trifluoromethanesulfonato)titanium(IV)

3. Powerful Claisen condensation and Claisen–aldol tandem reaction of α,α-dialkylated esters promoted by ZrCl4–iPr2NEt

4. A Highly Efficient Synthesis of Civetone

5. Practical Synthesis of (Z)-Civetone Utilizing Ti-Dieckmann Condensation

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