An Investigation of N-Aryl Sulfonation of 2-Azetidinone

RM Adlington; JE Baldwin; W McCoull; GJ Pritchard; CJ Schofield; Nicholas James Westwood

An Investigation of N-Aryl Sulfonation of 2-Azetidinone

RM Adlington, JE Baldwin, W McCoull, GJ Pritchard, CJ Schofield, Nicholas James Westwood

Research output: Other contribution

Abstract

N-Arylsulfonylation of 2-azetidinones can lead to the diastereoselective formation of oligomerization products. However, a simple increase of arylsulfonyl chloride concentration minimized oligomerization and allowed preparation of 1-arylsulfonyl-2-azetidinones in good yield.

Original language	English
Publication status	Published - 1997

Keywords

BETA-LACTAMS
INHIBITORS
DERIVATIVES

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@misc{d392bd7518d84594b4fb119bd40ec381,

title = "An Investigation of N-Aryl Sulfonation of 2-Azetidinone",

abstract = "N-Arylsulfonylation of 2-azetidinones can lead to the diastereoselective formation of oligomerization products. However, a simple increase of arylsulfonyl chloride concentration minimized oligomerization and allowed preparation of 1-arylsulfonyl-2-azetidinones in good yield.",

keywords = "BETA-LACTAMS, INHIBITORS, DERIVATIVES",

author = "RM Adlington and JE Baldwin and W McCoull and GJ Pritchard and CJ Schofield and Westwood, \{Nicholas James\}",

note = "Synth Commun",

year = "1997",

language = "English",

type = "Other",

}

TY - GEN

T1 - An Investigation of N-Aryl Sulfonation of 2-Azetidinone

AU - Adlington, RM

AU - Baldwin, JE

AU - McCoull, W

AU - Pritchard, GJ

AU - Schofield, CJ

AU - Westwood, Nicholas James

N1 - Synth Commun

PY - 1997

Y1 - 1997

N2 - N-Arylsulfonylation of 2-azetidinones can lead to the diastereoselective formation of oligomerization products. However, a simple increase of arylsulfonyl chloride concentration minimized oligomerization and allowed preparation of 1-arylsulfonyl-2-azetidinones in good yield.

AB - N-Arylsulfonylation of 2-azetidinones can lead to the diastereoselective formation of oligomerization products. However, a simple increase of arylsulfonyl chloride concentration minimized oligomerization and allowed preparation of 1-arylsulfonyl-2-azetidinones in good yield.

KW - BETA-LACTAMS

KW - INHIBITORS

KW - DERIVATIVES

M3 - Other contribution

ER -

An Investigation of N-Aryl Sulfonation of 2-Azetidinone

Abstract

Keywords

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