C-H bonds phosphorylation of ketene dithioacetals

Liping Zhu; Hongmei Yu; Quanping Guo; Qiao Chen; Zhaoqing Xu; Rui Wang

doi:10.1021/acs.orglett.5b00728

C-H bonds phosphorylation of ketene dithioacetals

Liping Zhu, Hongmei Yu, Quanping Guo, Qiao Chen, Zhaoqing Xu, Rui Wang

The Hong Kong Polytechnic University

Research output: Journal article publication › Journal article › Academic research › peer-review

60 Citations (Scopus)

Abstract

C-H bond phosphorylation of ketene dithioacetals was achieved under transition-metal-free or AgNO₃ mediated conditions. Synthetic transformations of the coupling product provided promising methods for the construction of highly functionalized phosphorylated N-heterocycles and tetrasubstituted alkenes.

Original language	English
Pages (from-to)	1978-1981
Number of pages	4
Journal	Organic Letters
Volume	17
Issue number	8
DOIs	https://doi.org/10.1021/acs.orglett.5b00728
Publication status	Published - 17 Apr 2015

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/acs.orglett.5b00728

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title = "C-H bonds phosphorylation of ketene dithioacetals",

abstract = "C-H bond phosphorylation of ketene dithioacetals was achieved under transition-metal-free or AgNO3 mediated conditions. Synthetic transformations of the coupling product provided promising methods for the construction of highly functionalized phosphorylated N-heterocycles and tetrasubstituted alkenes.",

author = "Liping Zhu and Hongmei Yu and Quanping Guo and Qiao Chen and Zhaoqing Xu and Rui Wang",

year = "2015",

month = apr,

day = "17",

doi = "10.1021/acs.orglett.5b00728",

language = "English",

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journal = "Organic Letters",

issn = "1523-7060",

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T1 - C-H bonds phosphorylation of ketene dithioacetals

AU - Zhu, Liping

AU - Yu, Hongmei

AU - Guo, Quanping

AU - Chen, Qiao

AU - Xu, Zhaoqing

AU - Wang, Rui

PY - 2015/4/17

Y1 - 2015/4/17

N2 - C-H bond phosphorylation of ketene dithioacetals was achieved under transition-metal-free or AgNO3 mediated conditions. Synthetic transformations of the coupling product provided promising methods for the construction of highly functionalized phosphorylated N-heterocycles and tetrasubstituted alkenes.

AB - C-H bond phosphorylation of ketene dithioacetals was achieved under transition-metal-free or AgNO3 mediated conditions. Synthetic transformations of the coupling product provided promising methods for the construction of highly functionalized phosphorylated N-heterocycles and tetrasubstituted alkenes.

UR - https://www.scopus.com/pages/publications/84928037102

U2 - 10.1021/acs.orglett.5b00728

DO - 10.1021/acs.orglett.5b00728

M3 - Journal article

SN - 1523-7060

VL - 17

SP - 1978

EP - 1981

JO - Organic Letters

JF - Organic Letters

IS - 8

ER -

C-H bonds phosphorylation of ketene dithioacetals

Abstract

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