Rationalising the effect of reducing agent on the oxazaborolidine-mediated asymmetric reduction of N-substituted imines

E.H.M. Kirton; G. Tughan; R.E. Morris; R.A. Field

doi:10.1016/j.tetlet.2003.11.021

Rationalising the effect of reducing agent on the oxazaborolidine-mediated asymmetric reduction of N-substituted imines

E.H.M. Kirton
, G. Tughan
, R.E. Morris
, R.A. Field

Manchester Institute of Biotechnology

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

Abstract

Comparing the effect of borane-based reducing agents on the stereochemical outcome of oxazaborolidine-mediated ketone and N-substituted imine reduction highlights the potential importance of reducing agent structure on the asymmetric sense of imine reduction.

Original language	Undefined
Pages (from-to)	853-855
Number of pages	3
Journal	Tetrahedron Letters
Volume	45
Issue number	4
DOIs	https://doi.org/10.1016/j.tetlet.2003.11.021
Publication status	Published - 19 Jan 2004

Research Beacons, Institutes and Platforms

Manchester Institute of Biotechnology

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10.1016/j.tetlet.2003.11.021

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title = "Rationalising the effect of reducing agent on the oxazaborolidine-mediated asymmetric reduction of N-substituted imines",

abstract = "Comparing the effect of borane-based reducing agents on the stereochemical outcome of oxazaborolidine-mediated ketone and N-substituted imine reduction highlights the potential importance of reducing agent structure on the asymmetric sense of imine reduction.",

author = "E.H.M. Kirton and G. Tughan and R.E. Morris and R.A. Field",

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AU - Kirton, E.H.M.

AU - Tughan, G.

AU - Morris, R.E.

AU - Field, R.A.

PY - 2004/1/19

Y1 - 2004/1/19

N2 - Comparing the effect of borane-based reducing agents on the stereochemical outcome of oxazaborolidine-mediated ketone and N-substituted imine reduction highlights the potential importance of reducing agent structure on the asymmetric sense of imine reduction.

AB - Comparing the effect of borane-based reducing agents on the stereochemical outcome of oxazaborolidine-mediated ketone and N-substituted imine reduction highlights the potential importance of reducing agent structure on the asymmetric sense of imine reduction.

UR - https://www.scopus.com/pages/publications/0346787842

U2 - 10.1016/j.tetlet.2003.11.021

DO - 10.1016/j.tetlet.2003.11.021

M3 - Article

SN - 0040-4039

VL - 45

SP - 853

EP - 855

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 4

ER -

Rationalising the effect of reducing agent on the oxazaborolidine-mediated asymmetric reduction of N-substituted imines

Abstract

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