Facile synthesis of spiropyrans from chromene hemiacetal esters and bifunctional nucleophiles

Yan Chao Wu; Hui Jing Li; Li Liu; Nicolas Demoulin; Zhe Liu; Dong Wang; Yong Jun Chen

doi:10.1055/s-0030-1260766

Facile synthesis of spiropyrans from chromene hemiacetal esters and bifunctional nucleophiles

Yan Chao Wu^*
, Hui Jing Li
, Li Liu
, Nicolas Demoulin
, Zhe Liu
, Dong Wang
, Yong Jun Chen

^*Corresponding author for this work

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

15 Scopus citations

Abstract

Facile synthesis of several new kinds of spiropyrans has been accomplished through the condensation of chromene hemi-acetal esters with bifunctional nuclephiles, in which previously nonpractical amination and amidation processes help each other and all become practical processes of the corresponding tandem reactions.

Original language	English
Pages (from-to)	1573-1578
Number of pages	6
Journal	Synlett
Issue number	11
DOIs	https://doi.org/10.1055/s-0030-1260766
State	Published - 2011
Externally published	Yes

Keywords

bifunctional nucleophile
chromene
hemiacetal ester
spiropyran
tandem reaction

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10.1055/s-0030-1260766

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title = "Facile synthesis of spiropyrans from chromene hemiacetal esters and bifunctional nucleophiles",

abstract = "Facile synthesis of several new kinds of spiropyrans has been accomplished through the condensation of chromene hemi-acetal esters with bifunctional nuclephiles, in which previously nonpractical amination and amidation processes help each other and all become practical processes of the corresponding tandem reactions.",

keywords = "bifunctional nucleophile, chromene, hemiacetal ester, spiropyran, tandem reaction",

author = "Wu, \{Yan Chao\} and Li, \{Hui Jing\} and Li Liu and Nicolas Demoulin and Zhe Liu and Dong Wang and Chen, \{Yong Jun\}",

year = "2011",

doi = "10.1055/s-0030-1260766",

language = "英语",

pages = "1573--1578",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "11",

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TY - JOUR

T1 - Facile synthesis of spiropyrans from chromene hemiacetal esters and bifunctional nucleophiles

AU - Wu, Yan Chao

AU - Li, Hui Jing

AU - Liu, Li

AU - Demoulin, Nicolas

AU - Liu, Zhe

AU - Wang, Dong

AU - Chen, Yong Jun

PY - 2011

Y1 - 2011

N2 - Facile synthesis of several new kinds of spiropyrans has been accomplished through the condensation of chromene hemi-acetal esters with bifunctional nuclephiles, in which previously nonpractical amination and amidation processes help each other and all become practical processes of the corresponding tandem reactions.

AB - Facile synthesis of several new kinds of spiropyrans has been accomplished through the condensation of chromene hemi-acetal esters with bifunctional nuclephiles, in which previously nonpractical amination and amidation processes help each other and all become practical processes of the corresponding tandem reactions.

KW - bifunctional nucleophile

KW - chromene

KW - hemiacetal ester

KW - spiropyran

KW - tandem reaction

UR - https://www.scopus.com/pages/publications/80955179610

U2 - 10.1055/s-0030-1260766

DO - 10.1055/s-0030-1260766

M3 - 文章

AN - SCOPUS:80955179610

SN - 0936-5214

SP - 1573

EP - 1578

JO - Synlett

JF - Synlett

IS - 11

ER -

Facile synthesis of spiropyrans from chromene hemiacetal esters and bifunctional nucleophiles

Abstract

Keywords

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