A novel route to arylacetones via a masked α-acylcarbonium intermediate

Shimon Shatzmiller; Ramy Lidor; Eytan Shalom; Eliezer Bahar

doi:10.1039/C39840000795

A novel route to arylacetones via a masked α-acylcarbonium intermediate

Shimon Shatzmiller, Ramy Lidor, Eytan Shalom, Eliezer Bahar

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

17 Scopus citations

Abstract

The Ag⁺ induced aromatic substitution reaction of bromoacetone O-methyloxime is described.

Original language	English
Pages (from-to)	795-796
Number of pages	2
Journal	Chemical Communications
Issue number	12
DOIs	https://doi.org/10.1039/C39840000795
State	Published - 1984
Externally published	Yes

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title = "A novel route to arylacetones via a masked α-acylcarbonium intermediate",

abstract = "The Ag+ induced aromatic substitution reaction of bromoacetone O-methyloxime is described.",

author = "Shimon Shatzmiller and Ramy Lidor and Eytan Shalom and Eliezer Bahar",

year = "1984",

doi = "10.1039/C39840000795",

language = "אנגלית",

pages = "795--796",

journal = "Chemical Communications",

issn = "0022-4936",

publisher = "Royal Society of Chemistry",

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AU - Shatzmiller, Shimon

AU - Lidor, Ramy

AU - Shalom, Eytan

AU - Bahar, Eliezer

PY - 1984

Y1 - 1984

N2 - The Ag+ induced aromatic substitution reaction of bromoacetone O-methyloxime is described.

AB - The Ag+ induced aromatic substitution reaction of bromoacetone O-methyloxime is described.

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AN - SCOPUS:37049095649

SN - 0022-4936

SP - 795

EP - 796

JO - Chemical Communications

JF - Chemical Communications

IS - 12

ER -

A novel route to arylacetones via a masked α-acylcarbonium intermediate

Abstract

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