In- or In(I)-Employed Diastereoselective Reformatsky-Type Reactions with Ketones: 1H NMR Investigations on the Active Species-Reference-Cited by-同舟云学术

In- or In(I)-Employed Diastereoselective Reformatsky-Type Reactions with Ketones: 1H NMR Investigations on the Active Species

Published:2004-10-27 Issue:24 Volume:6 Page:4475-4478
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Babu Srinivasarao Arulananda¹,Yasuda Makoto¹,Shibata Ikuya¹,Baba Akio¹

Affiliation:

1. Department of Molecular Chemistry and Handai Frontier Research Center, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0482846

Reference24 articles.

1. Neue Synthese zweiatomiger einbasischer Säuren aus den Ketonen

2. Recent Advancements in the Reformatsky Reaction

3. (b) Rathke, M. W.; Weipert, P. InComprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: New York, 1991; Vol. 2, p 277.

4. Activated Metals. XI. An Improved Procedure for the Preparation of β-Hydroxy Esters Using Activated Zinc1.

5. Use of the Zn-Cu Couple in the Reformatsky Reaction

Cited by 40 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Iron-mediated Reformatsky reaction of iododifluoromethyl ketones with aldehydes: Preparation of α,α-difluoro-β-hydroxyketone derivatives;Journal of Fluorine Chemistry;2023-07

2. Photoinduced reductive Reformatsky reaction of α-haloesters and aldehydes or ketones by cooperative dual-metal catalysis;Chemical Communications;2023

3. Miscellaneous Reactions;Applied Organic Chemistry;2020-12-11

4. Highly Catalytic Enantioselective Reformatsky Reaction with Aldehydes and Ketones Using an Available Prolinol Ligand;ACS Omega;2020-06-26

5. Synthesis of β-cyanoalanine and enantiomerically enriched aspartate derivatives via the Zn- or In-mediated nucleophilic addition to α-imino esters;Tetrahedron;2020-06