Stereoselective Approach to Multisubstituted Enolates from Unactivated Alkynes: Oxyalkylidenation of Alkynyl Ketone Enolates with Aldehydes-Reference-Cited by-同舟云学术

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Stereoselective Approach to Multisubstituted Enolates from Unactivated Alkynes: Oxyalkylidenation of Alkynyl Ketone Enolates with Aldehydes

Published:2023-09-21 Issue:19 Volume:88 Page:14096-14104
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sasaki Shuma¹,Kikuchi Jun¹^ORCID,Ito Shingo²^ORCID,Yoshikai Naohiko¹^ORCID

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan

2. School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, 21 Nanyang Link, Singapore 637371, Singapore

Funder

Agency for Science, Technology and Research

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Uehara Memorial Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c01615

Reference44 articles.

1. aKobayashi, S.; Yamashita, Y.; Yoo, W.J.; Kitanosono, T.; Soulé, J.F. In Comprehensive Organic Synthesis II; Knochel, P., Ed. Elsevier, 2014; Vol. 2, pp 396–450.

2. The Mukaiyama Aldol Reaction: 40 Years of Continuous Development

3. cStoltz, B. M.; Duquette, D. C.; Goldberg, A. F. G.; Liu, Y.; Loewinger, M. B.; Reeves, C. M. In Comprehensive Organic Synthesis II; Knochel, P., Ed. Elsevier, 2014; Vol. 3, pp 1–55.

4. Alkynes to (E)-enolates using tandem catalysis: stereoselective anti-aldol and syn-[3,3]-rearrangement reactions

5. The First Stereoselective Ficini−Claisen Rearrangement Using Chiral Ynamides

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