volume 21 issue 50 pages 18439-18444

Stereoselective Synthesis of Trisubstituted Alkenes through Sequential Iron-Catalyzed Reductiveanti-Carbozincation of Terminal Alkynes and Base-Metal-Catalyzed Negishi Cross-Coupling

Publication typeJournal Article
Publication date2015-11-04
scimago Q1
wos Q2
SJR0.981
CiteScore6.7
Impact factor3.7
ISSN09476539, 15213765
General Chemistry
Catalysis
Organic Chemistry
Abstract
The stereoselective synthesis of trisubstituted alkenes is challenging. Here, we show that an iron-catalyzed anti-selective carbozincation of terminal alkynes can be combined with a base-metal-catalyzed cross-coupling to prepare trisubstituted alkenes in a one-pot reaction and with high regio- and stereocontrol. Cu-, Ni-, and Co-based catalytic systems are developed for the coupling of sp-, sp(2) -, and sp(3) -hybridized carbon electrophiles, respectively. The method encompasses a large substrate scope, as various alkynyl, aryl, alkenyl, acyl, and alkyl halides are suitable coupling partners. Compared with conventional carbometalation reactions of alkynes, the current method avoids pre-made organometallic reagents and has a distinct stereoselectivity.
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Cheung C. W., Hu X. Stereoselective Synthesis of Trisubstituted Alkenes through Sequential Iron-Catalyzed Reductiveanti-Carbozincation of Terminal Alkynes and Base-Metal-Catalyzed Negishi Cross-Coupling // Chemistry - A European Journal. 2015. Vol. 21. No. 50. pp. 18439-18444.
GOST all authors (up to 50) Copy
Cheung C. W., Hu X. Stereoselective Synthesis of Trisubstituted Alkenes through Sequential Iron-Catalyzed Reductiveanti-Carbozincation of Terminal Alkynes and Base-Metal-Catalyzed Negishi Cross-Coupling // Chemistry - A European Journal. 2015. Vol. 21. No. 50. pp. 18439-18444.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1002/chem.201504049
UR - https://doi.org/10.1002/chem.201504049
TI - Stereoselective Synthesis of Trisubstituted Alkenes through Sequential Iron-Catalyzed Reductiveanti-Carbozincation of Terminal Alkynes and Base-Metal-Catalyzed Negishi Cross-Coupling
T2 - Chemistry - A European Journal
AU - Cheung, Chi Wai
AU - Hu, Xile
PY - 2015
DA - 2015/11/04
PB - Wiley
SP - 18439-18444
IS - 50
VL - 21
PMID - 26534875
SN - 0947-6539
SN - 1521-3765
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2015_Cheung,
author = {Chi Wai Cheung and Xile Hu},
title = {Stereoselective Synthesis of Trisubstituted Alkenes through Sequential Iron-Catalyzed Reductiveanti-Carbozincation of Terminal Alkynes and Base-Metal-Catalyzed Negishi Cross-Coupling},
journal = {Chemistry - A European Journal},
year = {2015},
volume = {21},
publisher = {Wiley},
month = {nov},
url = {https://doi.org/10.1002/chem.201504049},
number = {50},
pages = {18439--18444},
doi = {10.1002/chem.201504049}
}
MLA
Cite this
MLA Copy
Cheung, Chi Wai, and Xile Hu. “Stereoselective Synthesis of Trisubstituted Alkenes through Sequential Iron-Catalyzed Reductiveanti-Carbozincation of Terminal Alkynes and Base-Metal-Catalyzed Negishi Cross-Coupling.” Chemistry - A European Journal, vol. 21, no. 50, Nov. 2015, pp. 18439-18444. https://doi.org/10.1002/chem.201504049.