The reduction of some alicyclic- and aryl-substituted 3-acyl derivatives of 2-methylindole

Brian J Clark, R Grayshan, D D Miller

Research output: Contribution to journalArticle

Abstract

The structures of the products formed from the reduction of some 3-acyl derivatives of 2-methylindole were dependent on the nature of the substituent a to the carbonyl group and the reducing agent being used. When the substituent was aryl the only recoverable product had the hydrogenolysed structure; when the substituent was alicyclic the product had either the intermediate hydroxy or fully hydrogenolysed structure.

Original languageEnglish
Pages (from-to)2237-2240
Number of pages4
JournalJournal of the Chemical Society, Perkin Transactions 1
Publication statusPublished - 1983

Fingerprint

Reducing Agents
Derivatives
2-methylindole

Cite this

@article{149ed346b4fa4468824455603b8cabb8,
title = "The reduction of some alicyclic- and aryl-substituted 3-acyl derivatives of 2-methylindole",
abstract = "The structures of the products formed from the reduction of some 3-acyl derivatives of 2-methylindole were dependent on the nature of the substituent a to the carbonyl group and the reducing agent being used. When the substituent was aryl the only recoverable product had the hydrogenolysed structure; when the substituent was alicyclic the product had either the intermediate hydroxy or fully hydrogenolysed structure.",
author = "Clark, {Brian J} and R Grayshan and Miller, {D D}",
year = "1983",
language = "English",
pages = "2237--2240",
journal = "Journal of the Chemical Society, Perkin Transactions 1",
issn = "1472-7781",

}

The reduction of some alicyclic- and aryl-substituted 3-acyl derivatives of 2-methylindole. / Clark, Brian J; Grayshan, R; Miller, D D.

In: Journal of the Chemical Society, Perkin Transactions 1, 1983, p. 2237-2240.

Research output: Contribution to journalArticle

TY - JOUR

T1 - The reduction of some alicyclic- and aryl-substituted 3-acyl derivatives of 2-methylindole

AU - Clark, Brian J

AU - Grayshan, R

AU - Miller, D D

PY - 1983

Y1 - 1983

N2 - The structures of the products formed from the reduction of some 3-acyl derivatives of 2-methylindole were dependent on the nature of the substituent a to the carbonyl group and the reducing agent being used. When the substituent was aryl the only recoverable product had the hydrogenolysed structure; when the substituent was alicyclic the product had either the intermediate hydroxy or fully hydrogenolysed structure.

AB - The structures of the products formed from the reduction of some 3-acyl derivatives of 2-methylindole were dependent on the nature of the substituent a to the carbonyl group and the reducing agent being used. When the substituent was aryl the only recoverable product had the hydrogenolysed structure; when the substituent was alicyclic the product had either the intermediate hydroxy or fully hydrogenolysed structure.

UR - http://www.scopus.com/inward/record.url?scp=37049106139&partnerID=8YFLogxK

M3 - Article

SP - 2237

EP - 2240

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

SN - 1472-7781

ER -