Phosphine-Catalyzed Chemo- and Diastereoselective [2 + 2 + 2] and [3 + 2] Annulations of γ-Methyl Allenoates with Doubly Activated Olefins: Syntheses of Highly Substituted Cyclohexanes and Cyclopentenes-Reference-Cited by-同舟云学术

Phosphine-Catalyzed Chemo- and Diastereoselective [2 + 2 + 2] and [3 + 2] Annulations of γ-Methyl Allenoates with Doubly Activated Olefins: Syntheses of Highly Substituted Cyclohexanes and Cyclopentenes

Published:2019-09-12 Issue:19 Volume:84 Page:12490-12498
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Rongfang¹,Qin Zifeng²,Fan Binbin¹^ORCID,Li Ruifeng¹,Zhou Rong¹^ORCID,He Zhengjie³^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. China

2. Department of Applied Chemistry, China Agricultural University, Beijing 100193, P. R. China

3. The State Key Laboratory of Elemento-Organic Chemistry and College of Chemistry, Nankai University, Tianjin 300071, P. R. China

Funder

National Natural Science Foundation of China

the Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b01968

Reference57 articles.

1. Phosphine Organocatalysis in the Synthesis of Natural Products and Bioactive Compounds

2. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions

3. The Diels-Alder Reaction in Total Synthesis

4. Novel methods for the synthesis of three-, four-, five-, six- and seven-membered, saturated and partially unsaturated carbocycles

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