Triolborates: water-soluble complexes of arylboronic acids as precursors to iodoarenes
摘要:
A facile synthesis of aryl and heteroaryl iodides from water-soluble complexes of aryl- and heteroarylboronic acids has been developed. (C) 2010 Elsevier Ltd. All rights reserved.
REAGENT FOR ORGANIC SYNTHESIS REACTION CONTAINING ORGANIC TRIOL BORATE SALT
申请人:Miyaura Norio
公开号:US20100087646A1
公开(公告)日:2010-04-08
[Problem] To provide an organoboron compound-containing reagent for organic synthesis reactions which undergoes no trimerization with dehydration, does not necessitate activation with a base, and is stable and highly active.
[Means for Solving Problems] The reagent for organic synthesis reactions contains an organic triol borate salt represented by any of the general formulae (I) to (III) and general formula (XVI): (wherein R
1
represents alkyl, alkenyl, etc.; R
2
represents optionally substituted alkyl, alkenyl, alkynyl, etc. or represents hydrogen; m
+
represents an alkaline metal ion, phosphonium ion, or given ammonium ion; M
2+
represents an alkaline earth metal; X represents halogen or alkoxide; Y represents an alkali metal ion, etc.; A represents optionally substituted methylene; and n represents an integer).
Visible Light-Induced Selective Generation of Radicals from Organoborates by Photoredox Catalysis
作者:Yusuke Yasu、Takashi Koike、Munetaka Akita
DOI:10.1002/adsc.201200588
日期:2012.12.14
A new strategy for the generation of carbon-centered radicals via oxidation of alkyl-, allyl-, benzyl- and arylborates by visible-light-driven single electron transfer (SET) photoredoxcatalysis has been established. The generated radicals smoothly react with TEMPO and electron-deficient alkenes to afford CO and CC coupling products, respectively. In this radical initiating system, cyclic organo(triol)borates
NanoporousmetallicglassPd, which was fabricated by dealloying of a glassy metallic alloy Pd(30)Ni(50)P(20), exhibited a remarkable catalytic activity for the Suzuki-coupling reaction between iodoarenes and arylboronic acids under mild conditions. Moreover, the catalyst can be reused several times without a significant loss of catalytic activity.
Air- and moisture-stable Xantphos-ligated palladium dialkyl complex as a precatalyst for cross-coupling reactions
作者:Rina Takahashi、Koji Kubota、Hajime Ito
DOI:10.1039/c9cc06946a
日期:——
xantphos has been employed in a variety of palladium-catalyzed cross-couplingreactions, there has been little progress in developing Xantphos-ligated precatalysts. In this report, we describe a Xantphos-ligated palladium dialkyl complex that acts as a powerful precatalyst for C-N, C-S, and C-C cross-couplingreactions. This precatalyst is air- and moisture stable but can be thermally activated in the