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Journal ArticleDOI

Rhodium-catalyzed hydroborations of allylamine and allylimines

TLDR
The in situ rhodium-catalyzed addition of catecholborane (HBcat, cat = 1,2-O2C6H4) and pinacolboranes (HBpin, pin = 1 2 O2C2Me4) to allylamine, allylimine, 2- and 4-vinylpyridines, and a thienyl imi...
Abstract
The in situ rhodium-catalyzed addition of catecholborane (HBcat, cat = 1,2-O2C6H4) and pinacolborane (HBpin, pin = 1,2-O2C2Me4) to allylamine, allylimine, 2- and 4-vinylpyridines, and a thienyl imi...

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Journal ArticleDOI

Catalytic Asymmetric Hydroboration: Recent Advances and Applications in Carbon−Carbon Bond‐Forming Reactions

TL;DR: The metal-catalyzed hydroboration reaction provides access to functionalized organoboron derivatives that cannot be easily prepared using traditional reagents as discussed by the authors, including neoteric reaction media and novel ligands.
Journal ArticleDOI

Iron‐Catalyzed, Atom‐Economical, Chemo‐ and Regioselective Alkene Hydroboration with Pinacolborane

TL;DR: The synthesis of an electron-rich iron pincer complex and its application to the first example of iron-catalyzed alkene hydroboration of 4-methyl-1-pentene 1a with pinacolborane is reported.
Journal ArticleDOI

A Cobalt-Catalyzed Alkene Hydroboration with Pinacolborane†

TL;DR: An extremely efficient cobalt catalyst for the hydroboration of both vinylarenes and aliphatic α-olefins with pinacolborane is described, providing the anti-Markovnikov products with excellent regio- and chemoselectivity, broad functional-group tolerance, and high turnover numbers.
Journal ArticleDOI

Catalyst-free dehydrocoupling of amines, alcohols, and thiols with pinacol borane and 9-borabicyclononane (9-BBN)

TL;DR: The dehydrocoupling of pinacol borane and 9-borabicyclononane with a variety of amines, alcohols and thiols can be achieved under mild conditions without catalyst.
Journal ArticleDOI

Dramatic effect of Lewis acids on the rhodium-catalyzed hydroboration of olefins.

TL;DR: Preliminary mechanistic studies suggest that the B(C(6)F(5) needs to be present throughout the course of the reaction, not just at the initiation stage, and implicate this species, along with THF, in the heterolytic cleavage of the B-H bond of HBPin.
References
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Journal ArticleDOI

Palladium-catalyzed cross-coupling reactions of organoboron compounds

Norio Miyaura, +1 more
- 01 Nov 1995 - 
TL;DR: In this paper, a cross-coupling reaction is proposed for coupling 1 -Alkenylboron Derivatives: Synthesis of Conjugated Dienes 6.
Journal ArticleDOI

Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions

TL;DR: In this paper, the authors used Pd2(dba)3/P(t-Bu)3 as a catalyst for Suzuki cross-coupling of aryl and vinyl triflates.
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