A catalytic asymmetric one-pot [3+2] cyclization/semipinacol rearrangement sequence: an efficient construction of a multi-substituted 3H-spiro[benzofuran-2,1′-cyclopentane] skeleton-Reference-Cited by-同舟云学术

A catalytic asymmetric one-pot [3+2] cyclization/semipinacol rearrangement sequence: an efficient construction of a multi-substituted 3H-spiro[benzofuran-2,1′-cyclopentane] skeleton

Published:2019 Issue:26 Volume:55 Page:3789-3792
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Liu Lin¹²³⁴,Lei Lin-Sheng¹²³⁴,Zhan Zong-Song¹²³⁴,Liu Si-Zhan¹²³⁴,Wang Yu-Xiao¹²³⁴,Tu Yong-Qiang¹²³⁴^ORCID,Zhang Fu-Min¹²³⁴^ORCID,Zhang Xiao-Ming¹²³⁴^ORCID,Ma Ai-Jun⁵⁶⁷⁴,Wang Shao-Hua¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry & School of Pharmacy

2. Lanzhou University

3. Lanzhou 730000

4. P. R. China

5. School of Biotechnology and Health Science

6. Wuyi University

7. Jiangmen 529020

Abstract

We report an asymmetric construction of multi-substituted 3H-spiro[benzofuran-2,1’-cyclopentane]s with three new stereocenters and two new ring systems.

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC00811J

Reference56 articles.

1. Sesquiterpenes from the Red Alga Laurencia tristicha

2. Synthesis and Structural Revision of (±)-Laurentristich-4-ol

3. Design and Synthesis of 4,6-Di-tert-butyl-2,3-dihydro-5-benzofuranols as a Novel Series of Antiatherogenic Antioxidants

4. Novel Selective PDE4 Inhibitors. 2. Synthesis and Structure−Activity Relationships of 4-Aryl-Substituted cis-Tetra- and cis-Hexahydrophthalazinones

5. Novel Spirodihydrobenzofuranlactams as Antagonists of Endothelin and as Inhibitors of HIV-1 Protease Produced by Stachybotrys sp. I. Fermentation, Isolation and Biological Activity.

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