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Featured researches published by Niannian Yi.


Journal of Organic Chemistry | 2015

Copper/Iron-Catalyzed Aerobic Oxyphosphorylation of Terminal Alkynes Leading to β-Ketophosphonates

Niannian Yi; Ruijia Wang; Huaxu Zou; Weibao He; Wenqiang Fu; Weimin He

A copper/iron-catalyzed oxyphosphorylation of alkynes with H-phosphonates through a radical process was developed. The present protocol provides an attractive approach to β-ketophosphonates in moderate to good yields, with the advantages of readily available substrate, high functional group tolerance and operation simplicity.


Journal of Organic Chemistry | 2014

Method for transforming alkynes into (E)-dibromoalkenes.

Jiannan Xiang; Rui Yuan; Ruijia Wang; Niannian Yi; Linghui Lu; Huaxu Zou; Weimin He

The highly stereoselective bromination of alkynes has been realized by using copper(II) bromide as both the reacting partner and the catalyst, offering a generally efficient synthesis of (E)-dibromoalkenes. The reaction conditions are exceptionally mild, and a wide range of functional groups are well tolerated.


Organic Letters | 2016

Copper/Silver Cocatalyzed Oxidative Coupling of Vinylarenes with ICH2CF3 or ICH2CHF2 Leading to β-CF3/CHF2-Substituted Ketones

Niannian Yi; Hao Zhang; Chonghui Xu; Wei Deng; Ruijia Wang; Dongming Peng; Zebing Zeng; Jiannan Xiang

A novel copper/silver cocatalyzed oxidative coupling of vinylarenes with ICH2CF3 or ICH2CHF2 through a radical process has been developed. The transformation provides an attractive approach to β-CF3/CHF2-substituted ketones, with the advantages of easily available starting materials and operational simplicity.


Synthetic Communications | 2017

Synthesis of 3-acylated indoles through iron-catalyzed oxidative coupling of indoles with α-amino carbonyl compounds

Niannian Yi; Jinxia Li; Hao Zhang; Ruijia Wang; Jun Jiang; Wei Deng; Zebing Zeng; Jiannan Xiang

ABSTRACT A novel iron-catalyzed oxidative coupling of indoles with α-amino carbonyl compounds has been developed. The transformation provides an attractive approach to the synthesis of 3-acylindoles, with the advantages of easily available starting materials and high functional group tolerance. Furthermore, control experiments imply that a radical process maybe involved in this reaction. GRAPHICAL ABSTRACT


Organic and Biomolecular Chemistry | 2016

Fast regioselective sulfonylation of pyridine/quinoline N-oxides induced by iodine

Ruijia Wang; Zebing Zeng; Chuang Chen; Niannian Yi; Jun Jiang; Zhong Cao; Wei Deng; Jiannan Xiang


European Journal of Organic Chemistry | 2016

First Catalyzed Hydration of Halo­alkynes by a Recyclable Catalytic ­System

Huaxu Zou; Weibao He; Qizhi Dong; Ruijia Wang; Niannian Yi; Jun Jiang; Dongming Pen; Weimin He


Tetrahedron | 2015

Synthesis of β-ketophosphonates via AgNO3-catalyzed hydration of alkynylphosphonates: a rate-enhancement effect of methanol

Jiannan Xiang; Niannian Yi; Ruijia Wang; Linghui Lu; Huaxu Zou; Yuan Pan; Weimin He


Organic and Biomolecular Chemistry | 2017

Hypervalent iodine-triggered transformation of homopropargyl sulfonamides into dihalo-2,3-dihydropyrroles

Ruijia Wang; Yuejun OuYang; Chonghui Xu; Niannian Yi; Jun Jiang; Wei Deng; Zebing Zeng; Jiannan Xiang


Organic and Biomolecular Chemistry | 2017

PhI(OAc)2-mediated 1,2-aminohalogenation of alkynes: a general access to (E)-4-(halomethylene)oxazolidin-2-ones

Ruijia Wang; Huaxu Zou; Yi Xiong; Niannian Yi; Wei Deng; Jiannan Xiang


Chinese Journal of Chemistry | 2017

Synthesis of 2-Amino-1,3,4-oxadiazoles through Elemental Sulfur Promoted Cyclization of Hydrazides with Isocyanides

Wenhu Bao; Chuang Chen; Niannian Yi; Jun Jiang; Zebing Zeng; Wei Deng; Zhihong Peng; Jiannan Xiang

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