NHC-Catalyzed Atroposelective Acylation of Phenols: Access to Enantiopure NOBIN Analogs by Desymmetrization-Reference-Cited by-同舟云学术

NHC-Catalyzed Atroposelective Acylation of Phenols: Access to Enantiopure NOBIN Analogs by Desymmetrization

Published:2019-07-24 Issue:15 Volume:21 Page:6169-6172
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lu Shenci¹²,Poh Si Bei²,Rong Zi-Qiang¹²,Zhao Yu²³^ORCID

Affiliation:

1. Shaanxi Key Laboratory of Flexible Electronics, Northwestern Polytechnical University (NPU), 127 West Youyi Road, Xi’an 710072, China

2. Department of Chemistry, National University of Singapore, 3 Science Drive 3, Republic of Singapore, 117543

3. Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou 350207, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02425

Reference68 articles.

1. Privileged Chiral Ligands and Catalysts

2. Axially chiral bidentate ligands in asymmetric catalysis

3. 1,1′-Binaphthyl-2,2′-diol and 2,2′-diamino-1,1′-binaphthyl: versatile frameworks for chiral ligands in coordination and metallosupramolecular chemistry

4. Atroposelective Synthesis of Axially Chiral Biaryl Compounds

5. Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling

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