Thieme chemistry journal awardees - Where are they now? Asymmetric br?nsted acid catalyzed transfer hydrogenations

Magnus Rueping; Erli Sugiono; Fenja R. Schoepke

doi:10.1055/s-0029-1219528

Thieme chemistry journal awardees - Where are they now? Asymmetric br?nsted acid catalyzed transfer hydrogenations

Magnus Rueping^*, Erli Sugiono, Fenja R. Schoepke

^*Corresponding author for this work

Research output: Contribution to journal › Review article › peer-review

180 Scopus citations

Abstract

Asymmetric hydrogenations are of great importance in the synthesis of optically active amines. This account highlights the development of the first metal-free transfer hydrogenation that is both highly enantioselective and inspired by natures dehydrogen?ase. Further focus is given to the extension of this bioinspired process to provide a variety of valuable, biologically active products and natural products under mild reaction conditions.

Original language	English (US)
Pages (from-to)	852-865
Number of pages	14
Journal	Synlett
Issue number	6
DOIs	https://doi.org/10.1055/s-0029-1219528
State	Published - 2010
Externally published	Yes

Keywords

Asymmetric reduction
Binol phosphate
Br?nsted acid
Hantzsch ester
Organocatalysis
Transfer hydrogenation

ASJC Scopus subject areas

Organic Chemistry

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10.1055/s-0029-1219528

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title = "Thieme chemistry journal awardees - Where are they now? Asymmetric br?nsted acid catalyzed transfer hydrogenations",

abstract = "Asymmetric hydrogenations are of great importance in the synthesis of optically active amines. This account highlights the development of the first metal-free transfer hydrogenation that is both highly enantioselective and inspired by natures dehydrogen?ase. Further focus is given to the extension of this bioinspired process to provide a variety of valuable, biologically active products and natural products under mild reaction conditions.",

keywords = "Asymmetric reduction, Binol phosphate, Br?nsted acid, Hantzsch ester, Organocatalysis, Transfer hydrogenation",

author = "Magnus Rueping and Erli Sugiono and Schoepke, {Fenja R.}",

year = "2010",

doi = "10.1055/s-0029-1219528",

language = "English (US)",

pages = "852--865",

journal = "Synlett",

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T1 - Thieme chemistry journal awardees - Where are they now? Asymmetric br?nsted acid catalyzed transfer hydrogenations

AU - Rueping, Magnus

AU - Sugiono, Erli

AU - Schoepke, Fenja R.

PY - 2010

Y1 - 2010

N2 - Asymmetric hydrogenations are of great importance in the synthesis of optically active amines. This account highlights the development of the first metal-free transfer hydrogenation that is both highly enantioselective and inspired by natures dehydrogen?ase. Further focus is given to the extension of this bioinspired process to provide a variety of valuable, biologically active products and natural products under mild reaction conditions.

AB - Asymmetric hydrogenations are of great importance in the synthesis of optically active amines. This account highlights the development of the first metal-free transfer hydrogenation that is both highly enantioselective and inspired by natures dehydrogen?ase. Further focus is given to the extension of this bioinspired process to provide a variety of valuable, biologically active products and natural products under mild reaction conditions.

KW - Asymmetric reduction

KW - Binol phosphate

KW - Br?nsted acid

KW - Hantzsch ester

KW - Organocatalysis

KW - Transfer hydrogenation

UR - http://www.scopus.com/inward/record.url?scp=77949893012&partnerID=8YFLogxK

U2 - 10.1055/s-0029-1219528

DO - 10.1055/s-0029-1219528

M3 - Review article

AN - SCOPUS:77949893012

SN - 0936-5214

SP - 852

EP - 865

JO - Synlett

JF - Synlett

IS - 6

ER -

Thieme chemistry journal awardees - Where are they now? Asymmetric br?nsted acid catalyzed transfer hydrogenations

Abstract

Keywords

ASJC Scopus subject areas

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