Developing a bench-scale green diboration reaction toward industrial application

Albert Farre; Rachel Briggs; Cristina Pubill-Ulldemolins; Amadeu Bonet

doi:10.1055/s-0036-1590912

Developing a bench-scale green diboration reaction toward industrial application

Albert Farre, Rachel Briggs, Cristina Pubill-Ulldemolins^*, Amadeu Bonet

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

We report a new methodology for the organocatalytic diboration reaction using inexpensive, sustainable, nontoxic, commercially available halogen salts. This is an educative manuscript for the transformation of laboratory scale reactions into a sustainable approach of appeal to industry.

Original language	English
Pages (from-to)	4775-4782
Number of pages	8
Journal	Synthesis
Volume	49
Issue number	21
Early online date	10 Oct 2017
DOIs	https://doi.org/10.1055/s-0036-1590912
Publication status	Published - 2 Nov 2017

Keywords

Ate complexes
Boron chemistry
Green chemistry
Organocatalysis

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10.1055/s-0036-1590912

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title = "Developing a bench-scale green diboration reaction toward industrial application",

abstract = "We report a new methodology for the organocatalytic diboration reaction using inexpensive, sustainable, nontoxic, commercially available halogen salts. This is an educative manuscript for the transformation of laboratory scale reactions into a sustainable approach of appeal to industry.",

keywords = "Ate complexes, Boron chemistry, Green chemistry, Organocatalysis",

author = "Albert Farre and Rachel Briggs and Cristina Pubill-Ulldemolins and Amadeu Bonet",

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AU - Briggs, Rachel

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AU - Bonet, Amadeu

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AB - We report a new methodology for the organocatalytic diboration reaction using inexpensive, sustainable, nontoxic, commercially available halogen salts. This is an educative manuscript for the transformation of laboratory scale reactions into a sustainable approach of appeal to industry.

KW - Ate complexes

KW - Boron chemistry

KW - Green chemistry

KW - Organocatalysis

U2 - 10.1055/s-0036-1590912

DO - 10.1055/s-0036-1590912

M3 - Article

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VL - 49

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EP - 4782

JO - Synthesis

JF - Synthesis

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Developing a bench-scale green diboration reaction toward industrial application

Abstract

Keywords

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