Synthesis of Cyclopentenes, Pyrroles, and Thiophenes via a Sequence of Propargyl–Allenyl Isomerizations, Michael Additions, and Intramolecular Wittig Reactions-Reference-Cited by-同舟云学术

Synthesis of Cyclopentenes, Pyrroles, and Thiophenes via a Sequence of Propargyl–Allenyl Isomerizations, Michael Additions, and Intramolecular Wittig Reactions

Published:2014-11-04 Issue:22 Volume:79 Page:10867-10872
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhao Guoqing¹,Zhang Qianyun¹,Zhou Hongwei¹

Affiliation:

1. Department of Chemistry, Zhejiang University (Campus Xixi), Hangzhou 310028, People’s Republic of China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo501867h

Reference61 articles.

1. Phosphine-Catalyzed Rauhut-Currier Domino Reaction: A Facile Strategy for the Construction of Highly Functionalized Cyclopentene

2. Ring Expansion of Cyclobutylmethylcarbenium Ions to Cyclopentane or Cyclopentene Derivatives and Metal-Promoted Analogous Rearrangements

3. From Discovery to Application: 50 Years of the Vinylcyclopropane-Cyclopentene Rearrangement and Its Impact on the Synthesis of Natural Products

4. Multicomponent reactions for the synthesis of pyrroles

5. Pd-Catalyzed C–H Bond Functionalization on the Indole and Pyrrole Nucleus

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