Thiocyanation/Cyclization of γ-hydroxy Olefins to Access Thiocyanato-Containing Oxygen Heterocyclic Compounds

Chengcheng Li; Pingliang Long; Zhenda Fu; Di Wu; Fu Xue Chen; Hongquan Yin

doi:10.1002/ajoc.202100175

Thiocyanation/Cyclization of γ-hydroxy Olefins to Access Thiocyanato-Containing Oxygen Heterocyclic Compounds

Chengcheng Li, Pingliang Long, Zhenda Fu, Di Wu, Fu Xue Chen, Hongquan Yin^*

^*Corresponding author for this work

School of Chemistry and Chemical Engineering

Beijing Institute of Technology

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

9 Citations (Scopus)

Abstract

A new thiocyanation/cyclization reaction was developed to synthesize thiocyanato-containing oxygen heterocyclic compounds with terminal and non-terminal enols. The approach supplies an efficient method to build the multi-substituted ring and spiro ring structure of furan, which has a wide range of substrates, good functional group tolerance, and the desired products can be obtained in a medium to high yield.

Original language	English
Pages (from-to)	1643-1646
Number of pages	4
Journal	Asian Journal of Organic Chemistry
Volume	10
Issue number	7
DOIs	https://doi.org/10.1002/ajoc.202100175
Publication status	Published - Jul 2021

Keywords

cyclization
oxygen heterocyclic
spiro ring structure
thiocyanation

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10.1002/ajoc.202100175

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abstract = "A new thiocyanation/cyclization reaction was developed to synthesize thiocyanato-containing oxygen heterocyclic compounds with terminal and non-terminal enols. The approach supplies an efficient method to build the multi-substituted ring and spiro ring structure of furan, which has a wide range of substrates, good functional group tolerance, and the desired products can be obtained in a medium to high yield.",

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author = "Chengcheng Li and Pingliang Long and Zhenda Fu and Di Wu and Chen, {Fu Xue} and Hongquan Yin",

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AU - Li, Chengcheng

AU - Long, Pingliang

AU - Fu, Zhenda

AU - Wu, Di

AU - Chen, Fu Xue

AU - Yin, Hongquan

PY - 2021/7

Y1 - 2021/7

N2 - A new thiocyanation/cyclization reaction was developed to synthesize thiocyanato-containing oxygen heterocyclic compounds with terminal and non-terminal enols. The approach supplies an efficient method to build the multi-substituted ring and spiro ring structure of furan, which has a wide range of substrates, good functional group tolerance, and the desired products can be obtained in a medium to high yield.

AB - A new thiocyanation/cyclization reaction was developed to synthesize thiocyanato-containing oxygen heterocyclic compounds with terminal and non-terminal enols. The approach supplies an efficient method to build the multi-substituted ring and spiro ring structure of furan, which has a wide range of substrates, good functional group tolerance, and the desired products can be obtained in a medium to high yield.

KW - cyclization

KW - oxygen heterocyclic

KW - spiro ring structure

KW - thiocyanation

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U2 - 10.1002/ajoc.202100175

DO - 10.1002/ajoc.202100175

M3 - Article

AN - SCOPUS:85105048682

SN - 2193-5807

VL - 10

SP - 1643

EP - 1646

JO - Asian Journal of Organic Chemistry

JF - Asian Journal of Organic Chemistry

IS - 7

ER -

Thiocyanation/Cyclization of γ-hydroxy Olefins to Access Thiocyanato-Containing Oxygen Heterocyclic Compounds

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Keywords

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