4.6 Article

Copper-catalyzed regiodivergent 1,4-and 1,6-conjugate silyl addition to diendioates: access to functionalized allylsilanes

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 17, Issue 25, Pages 6122-6126

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ob01086f

Keywords

-

Funding

  1. Anhui Provincial Natural Science Foundation [1708085MB29]
  2. National Natural Science Foundation of China [21871240, 21672198]
  3. Fundamental Research Funds for the Central Universities [WK2060190082]
  4. State Key Program of National Natural Science Foundation of China [21432009]

Ask authors/readers for more resources

A copper-catalyzed regioselective 1,4- and 1,6-conjugate addition of a silyl reagent to diendioates was established. Various 1,4- and 1,6-protosilylation products were obtained in good yields and with high regioselectivity via tuning the ligands used in the reactions. This protocol has provided a simple and efficient method for the synthesis of multisubstituted functionalized allylsilanes.

Authors

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

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available