STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED AMINO-ALCOHOLS

B COATES; JF MALONE; MT MCCARNEY; PJ STEVENSON; Paul Stevenson

STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED AMINO-ALCOHOLS

B COATES, JF MALONE, MT MCCARNEY, PJ STEVENSON, Paul Stevenson

School of Chemistry and Chemical Engineering

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

2 Citations (Scopus)

Abstract

Acyclic amino alcohols can be obtained in high stereoisomeric purity by Stevens [2,3] rearrangement of tetrahydropyridine salts followed by reduction of the ketones and ring opening of the disubstituted pyrrolidine.

Original language	English
Pages (from-to)	2827-2828
Number of pages	2
Journal	Tetrahedron Letters
Volume	32
Issue number	24
Publication status	Published - 10 Jun 1991

Keywords

[2,3] SIGMATROPIC REARRANGEMENT
AMINO KETONE
AMINO ALCOHOL
CHELATION CONTROLLED REDUCTION

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@article{3d988d84472748608a25ff4fc30c1f38,

title = "STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED AMINO-ALCOHOLS",

abstract = "Acyclic amino alcohols can be obtained in high stereoisomeric purity by Stevens [2,3] rearrangement of tetrahydropyridine salts followed by reduction of the ketones and ring opening of the disubstituted pyrrolidine.",

keywords = "[2,3] SIGMATROPIC REARRANGEMENT, AMINO KETONE, AMINO ALCOHOL, CHELATION CONTROLLED REDUCTION",

author = "B COATES and JF MALONE and MT MCCARNEY and PJ STEVENSON and Paul Stevenson",

year = "1991",

month = jun,

day = "10",

language = "English",

volume = "32",

pages = "2827--2828",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "24",

}

TY - JOUR

T1 - STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED AMINO-ALCOHOLS

AU - COATES, B

AU - MALONE, JF

AU - MCCARNEY, MT

AU - STEVENSON, PJ

AU - Stevenson, Paul

PY - 1991/6/10

Y1 - 1991/6/10

N2 - Acyclic amino alcohols can be obtained in high stereoisomeric purity by Stevens [2,3] rearrangement of tetrahydropyridine salts followed by reduction of the ketones and ring opening of the disubstituted pyrrolidine.

AB - Acyclic amino alcohols can be obtained in high stereoisomeric purity by Stevens [2,3] rearrangement of tetrahydropyridine salts followed by reduction of the ketones and ring opening of the disubstituted pyrrolidine.

KW - [2,3] SIGMATROPIC REARRANGEMENT

KW - AMINO KETONE

KW - AMINO ALCOHOL

KW - CHELATION CONTROLLED REDUCTION

M3 - Article

SN - 0040-4039

VL - 32

SP - 2827

EP - 2828

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 24

ER -

STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED AMINO-ALCOHOLS

Abstract

Keywords

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