Stannous chloride reduction of α,β-unsaturated nitroalkenes

A direct synthesis of 2-aryl-2H-1-benzopyran-3(4H)-one oximes

Rajender S. Varma, Manju Varma, Yuan Z. Gai, George Kabalka

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Stannous chloride, in acetone, readily reduced the α,β-unsaturated nitroalkenes to the corresponding oximes at room temperature. A series of 2-aryl-3-chromanone oximes were obtained via the reduction of 3-nitrochromenes.

Original languageEnglish (US)
Pages (from-to)2581-2586
Number of pages6
JournalHeterocycles
Volume24
Issue number9
StatePublished - Sep 1 1986
Externally publishedYes

Fingerprint

Benzopyrans
Oximes
Acetone
Temperature
stannous chloride

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Stannous chloride reduction of α,β-unsaturated nitroalkenes : A direct synthesis of 2-aryl-2H-1-benzopyran-3(4H)-one oximes. / Varma, Rajender S.; Varma, Manju; Gai, Yuan Z.; Kabalka, George.

In: Heterocycles, Vol. 24, No. 9, 01.09.1986, p. 2581-2586.

Research output: Contribution to journalArticle

@article{27cc51f350904f2c8c1b15e29e754653,
title = "Stannous chloride reduction of α,β-unsaturated nitroalkenes: A direct synthesis of 2-aryl-2H-1-benzopyran-3(4H)-one oximes",
abstract = "Stannous chloride, in acetone, readily reduced the α,β-unsaturated nitroalkenes to the corresponding oximes at room temperature. A series of 2-aryl-3-chromanone oximes were obtained via the reduction of 3-nitrochromenes.",
author = "Varma, {Rajender S.} and Manju Varma and Gai, {Yuan Z.} and George Kabalka",
year = "1986",
month = "9",
day = "1",
language = "English (US)",
volume = "24",
pages = "2581--2586",
journal = "Heterocycles",
issn = "0385-5414",
publisher = "Japan Institute of Heterocyclic Chemistry",
number = "9",

}

TY - JOUR

T1 - Stannous chloride reduction of α,β-unsaturated nitroalkenes

T2 - A direct synthesis of 2-aryl-2H-1-benzopyran-3(4H)-one oximes

AU - Varma, Rajender S.

AU - Varma, Manju

AU - Gai, Yuan Z.

AU - Kabalka, George

PY - 1986/9/1

Y1 - 1986/9/1

N2 - Stannous chloride, in acetone, readily reduced the α,β-unsaturated nitroalkenes to the corresponding oximes at room temperature. A series of 2-aryl-3-chromanone oximes were obtained via the reduction of 3-nitrochromenes.

AB - Stannous chloride, in acetone, readily reduced the α,β-unsaturated nitroalkenes to the corresponding oximes at room temperature. A series of 2-aryl-3-chromanone oximes were obtained via the reduction of 3-nitrochromenes.

UR - http://www.scopus.com/inward/record.url?scp=46149135342&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=46149135342&partnerID=8YFLogxK

M3 - Article

VL - 24

SP - 2581

EP - 2586

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

IS - 9

ER -