Silver‐Catalyzed Asymmetric Aldol Reaction of Isocyanoacetic Acid Derivatives Enabled by Cooperative Participation of Classical and Nonclassical Hydrogen Bonds-Reference-Cited by-同舟云学术

Silver‐Catalyzed Asymmetric Aldol Reaction of Isocyanoacetic Acid Derivatives Enabled by Cooperative Participation of Classical and Nonclassical Hydrogen Bonds

Published:2022-06-21 Issue:14 Volume:364 Page:2333-2339
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv Synth Catal

Author:

Sakai Satoshi¹,Fujioka Akane¹,Imai Koji¹,Uchiyama Kei¹,Shimizu Yohei¹²^ORCID,Higashida Kosuke¹²,Sawamura Masaya¹²^ORCID

Affiliation:

1. Department of Chemistry Faculty of Science Hokkaido University Kita 10 Nishi 8, Kita-ku Sapporo Hokkaido 060-0810 Japan

2. Institute for Chemical Reaction Design and Discovery (WPI-ICReDD) Hokkaido University Kita 21 Nishi 10, Kita-ku Sapporo Hokkaido 001-0021 Japan

Publisher

Wiley

Subject

Organic Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200327

Reference48 articles.

2. Catalytic asymmetric aldol reaction: reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex

3. Catalytic asymmetric synthesis by means of secondary interaction between chiral ligands and substrates

4. M. Sawamura Y. Ito Asymmetric Aldol Reaction. inCatalytic Asymmetric Synthesis VCH Publishers Inc. 1997 pp 367–388.

5. For reviews on the use of isocyanoacetate derivatives in asymmetric catalysis see:

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