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Archive | 2011

The Chemistry of the Morita-Baylis-Hillman Reaction

Min Shi; Feijun Wang; Mei-Xin Zhao; Yin Wei

Morita-Baylis-Hillman Reaction Catalytic System for the Morita-Baylis-Hillman Reaction Transformations of Functional Groups in Morita-Baylis-Hillman Adducts Morita-Baylis-Hillman Adducts or Derivatives for the Construction of Cyclic Frameworks The application of Morita-Baylis-Hillman Reaction for the Synthesis of Natural Products


Beilstein Journal of Organic Chemistry | 2012

Synthesis of axially chiral oxazoline–carbene ligands with an N-naphthyl framework and a study of their coordination with AuCl·SMe2

Feijun Wang; Shengke Li; Mingliang Qu; Mei-Xin Zhao; Lian-jun Liu; Min Shi

Summary Axially chiral oxazoline–carbene ligands with an N-naphthyl framework were successfully prepared, and their coordination behavior with AuCl·SMe2 was also investigated, affording the corresponding Au(I) complexes in moderate to high yields.


Archive | 2011

Chapter 3:Transformations of Functional Groups in Morita–Baylis–Hillman Adducts

Mei-Xin Zhao; Yin Wei; Min Shi

This chapter will mainly describe the transformations of hydroxyl group in MBH adducts and the MBH adducts related Friedel-Crafts reaction, isomerization, Heck reaction, hydrogenation, Diels-Alder reaction as well as a variety of nucleophilic additions such as carbon nucleophiles, nitrogen nucleophiles and so on. Moreover, radical reaction and metathesis reaction of MBH adducts will also be discussed.


Archive | 2011

Chapter 2:Catalytic Systems for the Morita–Baylis–Hillman Reaction

Mei-Xin Zhao; Yin Wei; Min Shi

A remarkable number of effective catalysts have been identified and developed for Morita-Baylis-Hillman reaction and its asymmetric version. This Chapter will discuss achiral or chiral catalytic systems for the Morita-Baylis-Hillman reaction, which include amine-catalyzed system, phosphine-catalyzed system, Lewis acids-catalyzed system, co-catalyzed system, as well as polymer supported catalysts.


Archive | 2011

Chapter 1:Morita–Baylis–Hillman Reaction

Mei-Xin Zhao; Yin Wei; Min Shi

This Chapter will describe the origin and growth of Morita-Baylis-Hillman reaction, the reactant classes and reaction conditions, and also discuss the general catalytic mechanisms.


Journal of Organic Chemistry | 2008

Axially chiral BINIM and Ni(II)-catalyzed highly enantioselective 1,3-dipolar cycloaddition reactions of azomethine ylides and N-arylmaleimides.

Jing-Wen Shi; Mei-Xin Zhao; Zhi-Yu Lei; Min Shi


Tetrahedron Letters | 2007

A highly efficient asymmetric Michael addition of anthrone to nitroalkenes with cinchona organocatalysts

Min Shi; Zhi-Yu Lei; Mei-Xin Zhao; Jing-Wen Shi


Tetrahedron-asymmetry | 2010

Cu(I)-catalyzed asymmetric α-hydroxylation of β-keto esters in the presence of chiral phosphine-Schiff base-type ligands

Jia-Jun Jiang; Jian Huang; De Wang; Mei-Xin Zhao; Fei-Jun Wang; Min Shi


Beilstein Journal of Organic Chemistry | 2011

Synthesis of chiral mono(N-heterocyclic carbene) palladium and gold complexes with a 1,1'-biphenyl scaffold and their applications in catalysis

Lian-jun Liu; Feijun Wang; Wenfeng Wang; Mei-Xin Zhao; Min Shi


Tetrahedron-asymmetry | 2008

Bifunctional chiral phosphine-containing Lewis base catalyzed asymmetric Morita–Baylis–Hillman reaction of aldehydes with activated alkenes

Zhi-Yu Lei; Xu-Guang Liu; Min Shi; Mei-Xin Zhao

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Min Shi

Chinese Academy of Sciences

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Feijun Wang

East China University of Science and Technology

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Jia-Jun Jiang

East China University of Science and Technology

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De Wang

East China University of Science and Technology

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Jian Huang

East China University of Science and Technology

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Jun Zhang

East China University of Science and Technology

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Lian-jun Liu

Chinese Academy of Sciences

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Yin Wei

Chinese Academy of Sciences

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Zhi-Yu Lei

East China University of Science and Technology

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Jing-Wen Shi

East China University of Science and Technology

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