AuBr3- and Cu(OTf)2-Catalyzed Intramolecular [4 + 2] Cycloaddition of Tethered Alkynyl and Alkenyl Enynones and Enynals: A New Synthetic Method for Functionalized Polycyclic Hydrocarbons-Reference-Cited by-同舟云学术

AuBr3- and Cu(OTf)2-Catalyzed Intramolecular [4 + 2] Cycloaddition of Tethered Alkynyl and Alkenyl Enynones and Enynals: A New Synthetic Method for Functionalized Polycyclic Hydrocarbons

Published:2005-04-01 Issue:9 Volume:70 Page:3682-3685
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Asao Naoki¹,Sato Kenichiro¹,Menggenbateer ¹,Yamamoto Yoshinori¹

Affiliation:

1. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0500434

Reference18 articles.

1. Diastereoselection in Lewis-Acid-Mediated Aldol Additions

2. (e) Shambayati, S.; Schreiber, S. L. InComprehensive Organic Synthesis; Trost, B. M., Fleming I., Eds.; Pergamon Press: Oxford, 1991; Vol. 1, pp 283−324.

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