A chiral biselectrophile for efficient asymmetric synthesis in water

Olle Hidestål; Rui Ding; Ann Almesaker; Ulf Lindström

doi:10.1039/b415300f

A chiral biselectrophile for efficient asymmetric synthesis in water

Olle Hidestål, Rui Ding, Ann Almesaker, Ulf Lindström

Centre for Analysis and Synthesis

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

Abstract

The development of an efficient asymmetric dihydroxylation of 1,6-dibromodiene afforded a chiral biselectrophilic diol that displayed highly useful reactivity in water, as demonstrated by a three-step, two-pot asymmetric synthesis of a highly functionalized tetrahydrofuran.

Original language	English
Pages (from-to)	259-261
Journal	Green Chemistry
Volume	7
Issue number	5
DOIs	https://doi.org/10.1039/b415300f
Publication status	Published - 2005

Bibliographical note

The information about affiliations in this record was updated in December 2015.
The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)

Subject classification (UKÄ)

Organic Chemistry

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10.1039/b415300f

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@article{eca1c3169c7d43dba38ec88ff7972662,

title = "A chiral biselectrophile for efficient asymmetric synthesis in water",

abstract = "The development of an efficient asymmetric dihydroxylation of 1,6-dibromodiene afforded a chiral biselectrophilic diol that displayed highly useful reactivity in water, as demonstrated by a three-step, two-pot asymmetric synthesis of a highly functionalized tetrahydrofuran.",

author = "Olle Hidest{\aa}l and Rui Ding and Ann Almesaker and Ulf Lindstr{\"o}m",

note = "The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)",

year = "2005",

doi = "10.1039/b415300f",

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pages = "259--261",

journal = "Green Chemistry",

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publisher = "Royal Society of Chemistry",

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T1 - A chiral biselectrophile for efficient asymmetric synthesis in water

AU - Hidestål, Olle

AU - Ding, Rui

AU - Almesaker, Ann

AU - Lindström, Ulf

N1 - The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)

PY - 2005

Y1 - 2005

N2 - The development of an efficient asymmetric dihydroxylation of 1,6-dibromodiene afforded a chiral biselectrophilic diol that displayed highly useful reactivity in water, as demonstrated by a three-step, two-pot asymmetric synthesis of a highly functionalized tetrahydrofuran.

AB - The development of an efficient asymmetric dihydroxylation of 1,6-dibromodiene afforded a chiral biselectrophilic diol that displayed highly useful reactivity in water, as demonstrated by a three-step, two-pot asymmetric synthesis of a highly functionalized tetrahydrofuran.

U2 - 10.1039/b415300f

DO - 10.1039/b415300f

M3 - Article

SN - 1463-9270

VL - 7

SP - 259

EP - 261

JO - Green Chemistry

JF - Green Chemistry

IS - 5

ER -

A chiral biselectrophile for efficient asymmetric synthesis in water

Abstract

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