4.7 Article

Palladium-catalyzed Atroposelective Interannular C-H Arylation of Biaryl Aldehydes with Aryl Iodides Enabled by a Transient Directing Group Strategy

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 364, Issue 20, Pages 3589-3599

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.202200659

Keywords

Palladium; Atroposelectivity; C-H activation; Biaryl aldehyde; Transient directing group

Funding

  1. National Natural Science Foundation of China [21702237]
  2. Natural Science Foundation of Anhui Province [2108085MB60]
  3. Scientific Research Foundation of the Higher Education Institutions of Anhui Province [KJ2019 A0500]

Ask authors/readers for more resources

A concise method for the synthesis of axially chiral biaryl aldehydes has been developed through Pd/amino acid-catalyzed interannular C-H arylation of biaryl aldehydes with aryl iodides. This reaction exhibits excellent enantioselectivity and good tolerance towards functional groups. The scalability and potential utility of this asymmetric catalytic protocol have been highlighted.
A concise synthesis of axially chiral biaryl aldehydes through Pd/amino acid-catalyzed atroposelective interannular C-H arylation of biaryl aldehydes with aryl iodides is developed. This reaction proceeds smoothly involving excellent enantiocontrol and accomplishes with good tolerance of functional groups. Moreover, the readily accessible scale-up synthesis and further transformation of products has highlighted the potential utility of this asymmetric catalytic protocol.

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