ChemInform Abstract: Organocatalytic Asymmetric Conjugate Addition of 2‐Oxindole‐3‐carboxylate Esters to 2‐Phthalimido Acrylates: Efficient Synthesis of C<sup>γ</sup>‐Tetrasubstituted α‐Amino Acid Derivatives.

Gao, Juan; Chen, Jia‐Rong; Duan, Shu‐Wen; Li, Tian‐Ren; Lu, Liang‐Qiu; Xiao, Wen‐Jing

doi:10.1002/chin.201444111

ChemInform

2014

DOI: 10.1002/chin.201444111

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ChemInform Abstract: Organocatalytic Asymmetric Conjugate Addition of 2‐Oxindole‐3‐carboxylate Esters to 2‐Phthalimido Acrylates: Efficient Synthesis of C^γ‐Tetrasubstituted α‐Amino Acid Derivatives.

Juan Gao

Jia‐Rong Chen

Shu‐Wen Duan

et al.

Abstract: An asymmetric conjugate addition of 2‐oxoindole‐3‐carboxylates to 2‐activated phthalimidoacrylates using a bifunctional cinchona‐derived thiourea as the catalyst is presented.

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ChemInform Abstract: Organocatalytic Asymmetric Conjugate Addition of 2‐Oxindole‐3‐carboxylate Esters to 2‐Phthalimido Acrylates: Efficient Synthesis of C^γ‐Tetrasubstituted α‐Amino Acid Derivatives.

Abstract: An asymmetric conjugate addition of 2‐oxoindole‐3‐carboxylates to 2‐activated phthalimidoacrylates using a bifunctional cinchona‐derived thiourea as the catalyst is presented.

Cited by 0 publications

References 1 publication

No citations

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ChemInform Abstract: Organocatalytic Asymmetric Conjugate Addition of 2‐Oxindole‐3‐carboxylate Esters to 2‐Phthalimido Acrylates: Efficient Synthesis of Cγ‐Tetrasubstituted α‐Amino Acid Derivatives.

Abstract: An asymmetric conjugate addition of 2‐oxoindole‐3‐carboxylates to 2‐activated phthalimidoacrylates using a bifunctional cinchona‐derived thiourea as the catalyst is presented.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: Organocatalytic Asymmetric Conjugate Addition of 2‐Oxindole‐3‐carboxylate Esters to 2‐Phthalimido Acrylates: Efficient Synthesis of C^γ‐Tetrasubstituted α‐Amino Acid Derivatives.