Recyclable Helical Poly(phenyl isocyanide)-Supported l-Proline Catalyst for Direct Asymmetric Aldol Reaction in Brine

[1] James T(2015)Development and applications of disulfonimides in enantioselective organocatalysis Chem Rev 115 9388-9409

[2] Van Gemmeren M(2016)Enantioselective organocatalyzed transformations of β-ketoesters Chem Rev 116 9375-9437

[3] List B(2017)Organocatalysis in inert C-H bond functionalization Chem Rev 117 9433-9520

[4] Govender T(2008)The advent and development of organocatalysis Nature 455 304-308

[5] Arvidsson PI(2018)Construction of axially chiral compounds via asymmetric organocatalysis Acc Chem Res 51 534-547

[6] Maguire GEM(2010)Organocatalytic tunable amino acid polymers prepared by controlled radical polymerization Macromolecules 43 6374-6380

[7] Kruger HG(2015)Exerting control over the helical chirality in the main chain of sergeants- and -soldiers-type poly(quinoxaline-2,3-diyl)s by changing from random to block copolymerization protocols J Am Chem Soc 137 4070-4073

[8] Naicker T(2017)Significant improvement on enantioselectivity and diastereoselectivity of organocatalyzed asymmetric Aldol reaction using helical polyisocyanides bearing proline pendants ACS Macro Lett 6 824-829

[9] Qin Y(2015)Majority-rules type helical poly(quinoxaline-2,3-diyl)s as highly efficient chirality amplification systems for asymmetric catalysis Angew Chem Int Ed 54 9333-9337

[10] Zhu L(2018)Optically active helical polyisocyanides bearing chiral phosphine pendants: facile synthesis and application in enantioselective Rauhut-Currier reaction Chinese J Polym Sci 36 163-170

[1] James T(2015)Development and applications of disulfonimides in enantioselective organocatalysis Chem Rev 115 9388-9409

[2] Van Gemmeren M(2016)Enantioselective organocatalyzed transformations of β-ketoesters Chem Rev 116 9375-9437

[3] List B(2017)Organocatalysis in inert C-H bond functionalization Chem Rev 117 9433-9520

[4] Govender T(2008)The advent and development of organocatalysis Nature 455 304-308

[5] Arvidsson PI(2018)Construction of axially chiral compounds via asymmetric organocatalysis Acc Chem Res 51 534-547

[6] Maguire GEM(2010)Organocatalytic tunable amino acid polymers prepared by controlled radical polymerization Macromolecules 43 6374-6380

[7] Kruger HG(2015)Exerting control over the helical chirality in the main chain of sergeants- and -soldiers-type poly(quinoxaline-2,3-diyl)s by changing from random to block copolymerization protocols J Am Chem Soc 137 4070-4073

[8] Naicker T(2017)Significant improvement on enantioselectivity and diastereoselectivity of organocatalyzed asymmetric Aldol reaction using helical polyisocyanides bearing proline pendants ACS Macro Lett 6 824-829

[9] Qin Y(2015)Majority-rules type helical poly(quinoxaline-2,3-diyl)s as highly efficient chirality amplification systems for asymmetric catalysis Angew Chem Int Ed 54 9333-9337

[10] Zhu L(2018)Optically active helical polyisocyanides bearing chiral phosphine pendants: facile synthesis and application in enantioselective Rauhut-Currier reaction Chinese J Polym Sci 36 163-170