New chemistry of alkynyl trifluoroborates under transition metal catalyst-free conditions-Reference-Cited by-同舟云学术

New chemistry of alkynyl trifluoroborates under transition metal catalyst-free conditions

Published:2024 Issue: Volume: Page:
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Teng Shenghan¹^ORCID,Zhou Jianrong Steve²^ORCID,Huang Wei¹³

Affiliation:

1. Strait Laboratory of Flexible Electronics (SLoFE), Strait Institute of Flexible Electronics (SIFE, Future Technologies), Fujian Normal University, Fuzhou, 350117, China

2. State Key Laboratory of Chemical Oncogenomics, Shenzhen Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, 2199 Lishui Road, Nanshan District, Shenzhen 518055, China

3. Frontiers Science Center for Flexible Electronics (FSCFE), MIIT Key Laboratory of Flexible Electronics (KLoFE), Northwestern Polytechnical University, Xi'an, China

Abstract

This review summarizes recent advances in alkynyl trifluoroborate chemistry, emphasizing their unique reactivity and stability in organic synthesis and biological applications under transition metal catalyst-free conditions.

Funder

National Natural Science Foundation of China

Fujian Normal University

Shenzhen Graduate School, Peking University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO01398K

Reference118 articles.

1. Recent Developments in Organoboron Chemistry: Old Dogs, New Tricks

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3. Organotrifluoroborates: Another Branch of the Mighty Oak

4. Atom-Efficient Synthesis of Alkynylfluoroborates Using BF3 -Based Frustrated Lewis Pairs

5. Organotrifluoroborates: Protected Boronic Acids That Expand the Versatility of the Suzuki Coupling Reaction