作者:Chao Li、Jie Wang、Lisa M. Barton、Shan Yu、Maoqun Tian、David S. Peters、Manoj Kumar、Antony W. Yu、Kristen A. Johnson、Arnab K. Chatterjee、Ming Yan、Phil S. Baran
DOI:10.1126/science.aam7355
日期:2017.6.9
functionalized alkyl boronate esters from abundant carboxylic substituents. This broad-scope nickel-catalyzed reaction uses the same activating principle as amide bond formation to replace a carboxylic acid moiety with a boronate ester. Application to peptides allowed expedient preparations of α-amino boronic acids, often with high stereoselectivity, thereby facilitating synthesis of the alkyl boronic acid drugs
A copper(II)-catalyzed borylation of alkyl halides with bis(pinacolato)diboron (B2pin2) has been developed, which can be carried out in air, providing a wide range of primary, secondary, and some tertiary alkylboronates in high yields. A variety of functional groups are tolerated and the protocol is also applicable to unactivated alkyl chlorides (including 1,1- and 1,2-dichlorides). Preliminary mechanistic
Ni-catalyzed hydroboration and hydrosilylation of olefins with diboron and silylborane
作者:Toshiyuki Kamei、Sohshi Nishino、Toyoshi Shimada
DOI:10.1016/j.tetlet.2018.06.024
日期:2018.7
Herein we report a Ni-catalyzed formal hydroboration of olefins, which afforded anti-Markovnikov-type alkylboranes with B2pin2 and a stoichiometric amount of water. Formal hydrosilylation using air- and moisture-sensitive silylboranes also proceeded under optimized conditions. The reaction with trans-stilbene and D2O resulted in 1,2-H migration, which suggested that the reaction proceeded via β-hydride
Base-free nickel-catalyzed hydroboration of simple alkenes with bis(pinacolato)diboron in an alcoholic solvent
作者:Jiang-Fei Li、Zhen-Zhong Wei、Yong-Qiu Wang、Mengchun Ye
DOI:10.1039/c7gc02282d
日期:——
A base-free nickel-catalyzed hydroboration of unreactive simple alkenes with bis(pinacolato)diboron using methanol as the hydride source under mild conditions has been developed.
Iron-Catalyzed, Markovnikov-Selective Hydroboration of Styrenes
作者:Xu Chen、Zhaoyang Cheng、Zhan Lu
DOI:10.1021/acs.orglett.7b00227
日期:2017.3.3
A highly Markovnikov-selective, iron-catalyzed hydroboration of styrenes is reported using available oxazolinylphenyl picolinamide as the ligand to afford the branched hydroboration products with up to >50/1 b/l. This reaction is operationally simple and could be carried out in gram scale.
据报道,使用可用的恶唑啉基苯基吡啶甲酸酰胺作为配体,对苯乙烯进行了高度马尔科夫尼科夫选择性铁催化的硼氢化反应,以提供最高> 50/1 b / l的支链硼氢化产物。该反应操作简单,可以以克为单位进行。