Dependence of the Reactivities of Titanium Enolates on How They Are Generated: Diastereoselective Coupling of Phenylacetic Acid Esters Using Titanium Tetrachloride-Reference-Cited by-同舟云学术

Dependence of the Reactivities of Titanium Enolates on How They Are Generated: Diastereoselective Coupling of Phenylacetic Acid Esters Using Titanium Tetrachloride

Published:1996-01-01 Issue:8 Volume:61 Page:2809-2812
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Matsumura Yoshihiro¹,Nishimura Maiko¹,Hiu Hiroyuki¹,Watanabe Mitsuaki²,Kise Naoki³

Affiliation:

1. Faculty of Pharmaceutical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852, Japan

2. Center for Instrumental Analysis, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852, Japan

3. Department of Biotechnology, Faculty of Engineering, Tottori University, Koyama, Tottori 680, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo952204h

Reference18 articles.

1. Organotitanium Reagents in Organic Synthesis

2. Oxidative Dimerization of Lithium-Enolates of Esters Promoted by TitaniumTetrachloride

3. Novel and convenient route to substituted succinates. The dimerization of ketene silyl acetals promoted by titanium tetrachloride

4. Coupling reactions of vinylketene silyl acetals promoted by titanium tetrachloride

5. Lewis‐Säure‐bedingte α‐ tert ‐Alkylierung von Carbonsäuren und Carbonsäureestern

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