ChemInform Abstract: Highly Stereoselective [3 + 2] Cycloadditions of Chiral Palladium‐Containing N<sup>1</sup>‐1,3‐Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles.

Li, Tian‐Ren; Cheng, Bei‐Yi; Fan, Siqi; Wang, Ya‐Ni; Lu, Liang‐Qiu; Xiao, Wen‐Jing

doi:10.1002/chin.201636091

ChemInform

2016

DOI: 10.1002/chin.201636091

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ChemInform Abstract: Highly Stereoselective [3 + 2] Cycloadditions of Chiral Palladium‐Containing N¹‐1,3‐Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles.

Tian‐Ren Li

Bei‐Yi Cheng

Siqi Fan

et al.

Abstract: A catalytic asymmetric cycloaddition of 1,3‐dipoles, generated in situ by ring‐opening of aziridines, with 3‐methylene‐2‐oxindoles is developed furnishing spirooxindoles in high yields and excellent stereoselectivities.

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ChemInform Abstract: Highly Stereoselective [3 + 2] Cycloadditions of Chiral Palladium‐Containing N¹‐1,3‐Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles.

Abstract: A catalytic asymmetric cycloaddition of 1,3‐dipoles, generated in situ by ring‐opening of aziridines, with 3‐methylene‐2‐oxindoles is developed furnishing spirooxindoles in high yields and excellent stereoselectivities.

Cited by 0 publications

References 1 publication

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ChemInform Abstract: Highly Stereoselective [3 + 2] Cycloadditions of Chiral Palladium‐Containing N1‐1,3‐Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles.

Abstract: A catalytic asymmetric cycloaddition of 1,3‐dipoles, generated in situ by ring‐opening of aziridines, with 3‐methylene‐2‐oxindoles is developed furnishing spirooxindoles in high yields and excellent stereoselectivities.

Cited by 0 publications

References 1 publication

No citations

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ChemInform Abstract: Highly Stereoselective [3 + 2] Cycloadditions of Chiral Palladium‐Containing N¹‐1,3‐Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles.