4.7 Article

Gold-Catalyzed Reactions between Alkenyldiazo Carbonyl Species and Acetals

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 78, Issue 11, Pages 5711-5716

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo400419d

Keywords

-

Funding

  1. National Science Council, Taiwan

Ask authors/readers for more resources

In the presence of catalyst IPrAuSbF6 catalyst (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene), alkenyldiazo carbonyl species react with organic acetals to give E-configured alkyl 3,5-dimethoxy-5-pent-2-enoates stereoselectively. This reaction sequence comprises an initial Prins-type reaction, followed by gold carbene formation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available