Thieme chemistry journal awardees - Where are they now? aldol synthesis by anti-markovnikov hydration of propargyloxy substrates: Feasibility, stereospecifity, and reiterative alkynylation-hydration

Lukas Hintermann; Thomas Kribber; Aurélie Labonne; Eva Paciok

doi:10.1055/s-0029-1217734

Thieme chemistry journal awardees - Where are they now? aldol synthesis by anti-markovnikov hydration of propargyloxy substrates: Feasibility, stereospecifity, and reiterative alkynylation-hydration

Lukas Hintermann
, Thomas Kribber
, Aurélie Labonne
, Eva Paciok

RWTH Aachen University

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

25 Scopus citations

Abstract

Aldol derivatives have been synthesized by redox-neutral catalytic anti-Markovnikov hydration of propargyloxy sub-strates. A reiterative sequence of aldehyde alkynylation and alkyne hydration leads to 1,3-polyol derivatives.

Original language	English
Pages (from-to)	2412-2416
Number of pages	5
Journal	Synlett
Issue number	15
DOIs	https://doi.org/10.1055/s-0029-1217734
State	Published - Sep 2009
Externally published	Yes

Keywords

Addition reactions
Aldehydes
Alkynes
Homogeneous catalysis
Ruthenium

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10.1055/s-0029-1217734

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title = "Thieme chemistry journal awardees - Where are they now? aldol synthesis by anti-markovnikov hydration of propargyloxy substrates: Feasibility, stereospecifity, and reiterative alkynylation-hydration",

abstract = "Aldol derivatives have been synthesized by redox-neutral catalytic anti-Markovnikov hydration of propargyloxy sub-strates. A reiterative sequence of aldehyde alkynylation and alkyne hydration leads to 1,3-polyol derivatives.",

keywords = "Addition reactions, Aldehydes, Alkynes, Homogeneous catalysis, Ruthenium",

author = "Lukas Hintermann and Thomas Kribber and Aur{\'e}lie Labonne and Eva Paciok",

year = "2009",

month = sep,

doi = "10.1055/s-0029-1217734",

language = "English",

pages = "2412--2416",

journal = "Synlett",

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publisher = "Georg Thieme Verlag",

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Thieme chemistry journal awardees - Where are they now? aldol synthesis by anti-markovnikov hydration of propargyloxy substrates: Feasibility, stereospecifity, and reiterative alkynylation-hydration. / Hintermann, Lukas; Kribber, Thomas; Labonne, Aurélie et al.
In: Synlett, No. 15, 09.2009, p. 2412-2416.

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

TY - JOUR

T1 - Thieme chemistry journal awardees - Where are they now? aldol synthesis by anti-markovnikov hydration of propargyloxy substrates

T2 - Feasibility, stereospecifity, and reiterative alkynylation-hydration

AU - Hintermann, Lukas

AU - Kribber, Thomas

AU - Labonne, Aurélie

AU - Paciok, Eva

PY - 2009/9

Y1 - 2009/9

N2 - Aldol derivatives have been synthesized by redox-neutral catalytic anti-Markovnikov hydration of propargyloxy sub-strates. A reiterative sequence of aldehyde alkynylation and alkyne hydration leads to 1,3-polyol derivatives.

AB - Aldol derivatives have been synthesized by redox-neutral catalytic anti-Markovnikov hydration of propargyloxy sub-strates. A reiterative sequence of aldehyde alkynylation and alkyne hydration leads to 1,3-polyol derivatives.

KW - Addition reactions

KW - Aldehydes

KW - Alkynes

KW - Homogeneous catalysis

KW - Ruthenium

UR - https://www.scopus.com/pages/publications/70349275870

U2 - 10.1055/s-0029-1217734

DO - 10.1055/s-0029-1217734

M3 - Article

AN - SCOPUS:70349275870

SN - 0936-5214

SP - 2412

EP - 2416

JO - Synlett

JF - Synlett

IS - 15

ER -

Thieme chemistry journal awardees - Where are they now? aldol synthesis by anti-markovnikov hydration of propargyloxy substrates: Feasibility, stereospecifity, and reiterative alkynylation-hydration

Abstract

Keywords

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