Synthesis of some 5-substituted indoles

Youhua Yang; Arnold R. Martin; David L. Nelson; John Regan

doi:10.3987/com-92-6009

Synthesis of some 5-substituted indoles

Youhua Yang, Arnold R. Martin, David L. Nelson, John Regan

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

39 Scopus citations

Abstract

A halogen-metal exchange strategy was employed to prepare several 5-substituted indoles from 5-bromoindole. Additional derivatives were elaborated from the formyl, acetyl, thiomethyl, boronic acid and trimethylstannyl analogues thus prepared.

Original language	English (US)
Pages (from-to)	1169-1175
Number of pages	7
Journal	Heterocycles
Volume	34
Issue number	6
DOIs	https://doi.org/10.3987/com-92-6009
State	Published - Jun 1 1992

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

Access to Document

10.3987/com-92-6009

Cite this

@article{d0129e7ded7240eb840b0156bcdec235,

title = "Synthesis of some 5-substituted indoles",

abstract = "A halogen-metal exchange strategy was employed to prepare several 5-substituted indoles from 5-bromoindole. Additional derivatives were elaborated from the formyl, acetyl, thiomethyl, boronic acid and trimethylstannyl analogues thus prepared.",

author = "Youhua Yang and Martin, {Arnold R.} and Nelson, {David L.} and John Regan",

year = "1992",

month = jun,

day = "1",

doi = "10.3987/com-92-6009",

language = "English (US)",

volume = "34",

pages = "1169--1175",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "6",

}

TY - JOUR

T1 - Synthesis of some 5-substituted indoles

AU - Yang, Youhua

AU - Martin, Arnold R.

AU - Nelson, David L.

AU - Regan, John

PY - 1992/6/1

Y1 - 1992/6/1

N2 - A halogen-metal exchange strategy was employed to prepare several 5-substituted indoles from 5-bromoindole. Additional derivatives were elaborated from the formyl, acetyl, thiomethyl, boronic acid and trimethylstannyl analogues thus prepared.

AB - A halogen-metal exchange strategy was employed to prepare several 5-substituted indoles from 5-bromoindole. Additional derivatives were elaborated from the formyl, acetyl, thiomethyl, boronic acid and trimethylstannyl analogues thus prepared.

UR - http://www.scopus.com/inward/record.url?scp=0001627456&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0001627456&partnerID=8YFLogxK

U2 - 10.3987/com-92-6009

DO - 10.3987/com-92-6009

M3 - Article

AN - SCOPUS:0001627456

VL - 34

SP - 1169

EP - 1175

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

IS - 6

ER -

Synthesis of some 5-substituted indoles

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this