CuBr-Catalyzed Coupling of Propargyl Bromides with Terminal Alkynes: Syntheses of 1,4-Diynes and Alkynyl Shift Access to Unsymmetrical 1, <i>n</i>-Diynes-Reference-Cited by-同舟云学术

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CuBr-Catalyzed Coupling of Propargyl Bromides with Terminal Alkynes: Syntheses of 1,4-Diynes and Alkynyl Shift Access to Unsymmetrical 1, n-Diynes

Published:2024-06-06 Issue:12 Volume:89 Page:8851-8860
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wang Yunpeng¹,Lv Jiaying¹,Hua Ruimao¹²^ORCID

Affiliation:

1. Key Laboratory of Organic Optoelectronics & Molecular Engineering of Ministry of Education, Department of Chemistry, Tsinghua University, Beijing 100084, China

2. State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, College of Chemistry, Xinjiang University, Urumqi 830017, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00733

Reference32 articles.

1. Hydroelementation of diynes

2. One step synthesis of [7]metacyclophanediyne complexes from bis(propargyldicobalt) dication equivalents

3. Total Synthesis of (+)-Mesembrine Applying Asymmetric Gold Catalysis

4. Construction of (Z,Z ) skipped 1,4-dienes. Application to the synthesis of polyunsaturated fatty acids and derivatives †

5. Photosensitised oxidation of model unsaturated lipid systems: (4Z,7Z)-undeca-4,7-diene and (4Z)-undec-4-en-7-yne

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