Transition Metal/Base-Catalyzed Aldol Reactions of Isocyanoacetic Acid Derivatives with Prochiral Ketones, a Straightforward Approach to Stereochemically Defined β,β-Disubstituted-β-hydroxy-α-amino Acids.1 Scope and Limitations-Reference-Cited by-同舟云学术

Transition Metal/Base-Catalyzed Aldol Reactions of Isocyanoacetic Acid Derivatives with Prochiral Ketones, a Straightforward Approach to Stereochemically Defined β,β-Disubstituted-β-hydroxy-α-amino Acids.1 Scope and Limitations

Published:1997-05-01 Issue:11 Volume:62 Page:3470-3479
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Soloshonok Vadim A.¹,Kacharov Alexey D.¹,Avilov Dimitry V.¹,Ishikawa Kohki¹,Nagashima Nobuya¹,Hayashi Tamio¹

Affiliation:

1. National Industrial Research Institute of Nagoya, Hirate-cho 1-1, Kita-ku, Nagoya City, Aichi Prefecture 462, Japan, Institute of Bioorganic Chemistry and Petrochemistry, Ukrainian Academy of Sciences, Kiev 253160, Ukraine, Central Research Laboratories of Ajinomoto Co., Inc., Suzukicho, Kawasaki 210, Japan, and Department of Chemistry, Faculty of Science, Kyoto University, Sakyo, Kyoto 606-01, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9623402

Reference66 articles.

1. Highly diastereoselective aldol reaction of fluoroalkyl aryl ketones with methyl isocyanoacetate catalyzed by silver(I)/triethylamine

2. Stereoselective Aldol Reactions withα-Unsubstituted Chiral Enolates

3. In Organic Chemistry Series;For,1989

4. Structure-conformation-activity relationships of renin inhibitory peptides having P1-P1' Xaaψ[CH2NH]Yaa substitutions: molecular modeling and crystallography studies1

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