Organocatalytic highly enantioselective α-selenenylation of aldehydes

Henrik Sundén; Ramon Rios; Armando Córdova

doi:10.1016/j.tetlet.2007.08.125

Organocatalytic highly enantioselective α-selenenylation of aldehydes

Henrik Sundén
, Ramon Rios
, Armando Córdova

Chemistry

Arrhenius Laboratory

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

57 Scopus citations

Abstract

The highly enantioselective organocatalytic α-selenenylation of aldehydes is presented. The reaction gives access to α-phenylselenoaldehydes and β-selenoalcohols in high yields with up to >99% ee.

Original language	British English
Pages (from-to)	7865-7869
Number of pages	5
Journal	Tetrahedron Letters
Volume	48
Issue number	44
DOIs	https://doi.org/10.1016/j.tetlet.2007.08.125
State	Published - 29 Oct 2007

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@article{55dbc46a42f84ab1a3e1686726ef8251,

title = "Organocatalytic highly enantioselective α-selenenylation of aldehydes",

abstract = "The highly enantioselective organocatalytic α-selenenylation of aldehydes is presented. The reaction gives access to α-phenylselenoaldehydes and β-selenoalcohols in high yields with up to >99\% ee.",

author = "Henrik Sund{\'e}n and Ramon Rios and Armando C{\'o}rdova",

note = "Funding Information: We gratefully acknowledge the Swedish National Research Council, Wenner-Gren and Carl-Trygger Foundations for financial support. ",

year = "2007",

month = oct,

day = "29",

doi = "10.1016/j.tetlet.2007.08.125",

language = "British English",

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journal = "Tetrahedron Letters",

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T1 - Organocatalytic highly enantioselective α-selenenylation of aldehydes

AU - Sundén, Henrik

AU - Rios, Ramon

AU - Córdova, Armando

N1 - Funding Information: We gratefully acknowledge the Swedish National Research Council, Wenner-Gren and Carl-Trygger Foundations for financial support.

PY - 2007/10/29

Y1 - 2007/10/29

N2 - The highly enantioselective organocatalytic α-selenenylation of aldehydes is presented. The reaction gives access to α-phenylselenoaldehydes and β-selenoalcohols in high yields with up to >99% ee.

AB - The highly enantioselective organocatalytic α-selenenylation of aldehydes is presented. The reaction gives access to α-phenylselenoaldehydes and β-selenoalcohols in high yields with up to >99% ee.

UR - https://www.scopus.com/pages/publications/34848856348

U2 - 10.1016/j.tetlet.2007.08.125

DO - 10.1016/j.tetlet.2007.08.125

M3 - Article

AN - SCOPUS:34848856348

SN - 0040-4039

VL - 48

SP - 7865

EP - 7869

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 44

ER -

Organocatalytic highly enantioselective α-selenenylation of aldehydes

Abstract

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