» Articles » PMID: 25665129

Highly Regio- and Stereoselective Synthesis of Boron-substituted Enynes Via Copper-catalyzed Borylation of Conjugated Diynes

Overview
Journal Org Lett
Specialties Biochemistry
Chemistry
Date 2015 Feb 10
PMID 25665129
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

A mild copper-catalyzed regio- and stereoselective monoborylation of conjugated diynes with bis(pinacolato)diboron that affords enynylboronates is reported. The reaction is efficient for different types of conjugated diynes including unsymmetrical diynes and produces enynylboron compounds with high and complementary regioselectivity compared with classical hydrometalation reactions. In particular, the reactions of internal conjugated diynes with a silyl substitution produced highly functionalized enynes with high regio- and stereoselectivity, which can be used in further transformations.

Citing Articles

Chemo-, Regio-, and Stereoselective -Hydroboration of 1,3-Enynes: Copper-Catalyzed Access to ()- and ()-2-Boryl-1,3-dienes.

Buchbinder N, Nguyen L, Beck O, Bage A, Slebodnick C, Santos W Org Lett. 2024; 26(29):6136-6141.

PMID: 39018130 PMC: 11287746. DOI: 10.1021/acs.orglett.4c01929.


[Pt(PPh)]-Catalyzed Selective Diboration of Symmetrical and Unsymmetrical 1,3-Diynes.

Szyling J, Szymanska A, Franczyk A, Walkowiak J J Org Chem. 2022; 87(16):10651-10663.

PMID: 35917577 PMC: 9396666. DOI: 10.1021/acs.joc.2c00844.


Transition Metal-Free Regio- and Stereo-Selective trans Hydroboration of 1,3-Diynes: A Phosphine-Catalyzed Access to (E)-1-Boryl-1,3-Enynes.

Jos S, Szwetkowski C, Slebodnick C, Ricker R, Lok Chan K, Chan W Chemistry. 2022; 28(63):e202202349.

PMID: 35917135 PMC: 9804376. DOI: 10.1002/chem.202202349.