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Your search keyword '"Chen, Xin-Meng"' showing total 2 results
Start Over Author "Chen, Xin-Meng" Publisher wiley-blackwell
2 results on '"Chen, Xin-Meng"'

1. Chiral Indoline‐2‐carboxylic Acid Enables Highly Enantioselective Catellani‐type Annulation with 4‐(Bromomethyl)cyclohexanone.

Author

Chen, Xin‐Meng, Zhu, Ling, Chen, Dian‐Feng, and Gong, Liu‐Zhu

Subjects
*CYCLOHEXANONES, *ANNULATION, *BORONIC acids, *AMINO acids, *ACIDS
Abstract

Chiral indoline‐2‐carboxylic acid has been identified to enable a highly enantioselective Catellani‐type annulation of (hetero)aryl, alkenyl triflate and conjugated vinyl iodides with 4‐(bromomethyl)cyclohexanone, directly assembling a diverse range of chiral all‐carbon bridged ring systems. Control experiments and DFT calculations suggest that the coordinating orientation of the chiral amino acid to the arylpalladium(II) center allows for high levels of stereochemical control. [ABSTRACT FROM AUTHOR]

Published
2021
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2. Chiral Indoline‐2‐carboxylic Acid Enables Highly Enantioselective Catellani‐type Annulation with 4‐(Bromomethyl)cyclohexanone.

Author

Chen, Xin‐Meng, Zhu, Ling, Chen, Dian‐Feng, and Gong, Liu‐Zhu

Subjects
*CYCLOHEXANONES, *ANNULATION, *BORONIC acids, *AMINO acids, *ACIDS
Abstract

Chiral indoline‐2‐carboxylic acid has been identified to enable a highly enantioselective Catellani‐type annulation of (hetero)aryl, alkenyl triflate and conjugated vinyl iodides with 4‐(bromomethyl)cyclohexanone, directly assembling a diverse range of chiral all‐carbon bridged ring systems. Control experiments and DFT calculations suggest that the coordinating orientation of the chiral amino acid to the arylpalladium(II) center allows for high levels of stereochemical control. [ABSTRACT FROM AUTHOR]

Published
2021
Full Text
View/download PDF

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