Phosphine-Catalyzed Asymmetric (3+2) Annulations of δ-Acetoxy Allenoates with 2-Naphthols-Reference-Cited by-同舟云学术

Phosphine-Catalyzed Asymmetric (3+2) Annulations of δ-Acetoxy Allenoates with 2-Naphthols

Published:2017-11-20 Issue:23 Volume:19 Page:6392-6395
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Dong¹,Tong Xiaofeng¹^ORCID

Affiliation:

1. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, 1 Gehu Road, Changzhou, 213164, China

Funder

National Natural Science Foundation of China

Jiangsu Province

Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b03250

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1. Stereochemistry of the active site of α-chymotrypsin

2. Bicyclic N-Hydroxyurea Inhibitors of 5-Lipoxygenase: Pharmacodynamic, Pharmacokinetic, and in Vitro Metabolic Studies Characterizing N-Hydroxy-N-(2,3-dihydro-6-(phenylmethoxy)-3-benzofuranyl)urea

3. C17,20-lyase inhibitors. Part 2: Design, synthesis and structure–activity relationships of (2-naphthylmethyl)-1H-imidazoles as novel C17,20-lyase inhibitors

4. Iron-Catalyzed Oxidative Cross-Coupling of Phenols and Alkenes

5. Convenient synthesis of novel 2,2-dialkyl-1,2-dihydronaphtho[2,1-b]furans

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