Novel amide-functionalized chloramphenicol base bifunctional organocatalysts for enantioselective alcoholysis of meso-cyclic anhydrides.

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Novel amide-functionalized chloramphenicol base bifunctional organocatalysts for enantioselective alcoholysis of meso-cyclic anhydrides.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

@zh-my

2018年学术文章

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2018年學術文章

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2018年學術文章

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name

Novel amide-functionalized chl ...... sis of meso-cyclic anhydrides.

@en

Novel amide-functionalized chl ...... sis of meso-cyclic anhydrides.

@nl

type

Item

label

Novel amide-functionalized chl ...... sis of meso-cyclic anhydrides.

@en

Novel amide-functionalized chl ...... sis of meso-cyclic anhydrides.

@nl

prefLabel

Novel amide-functionalized chl ...... sis of meso-cyclic anhydrides.

@en

Novel amide-functionalized chl ...... sis of meso-cyclic anhydrides.

@nl

P1476

Novel amide-functionalized chl ...... ysis of meso-cyclic anhydrides

@en

P2093

Fener Chen

http://www.w3.org/2001/XMLSchema#string

Haifeng Wang

http://www.w3.org/2001/XMLSchema#string

Haihui Peng

http://www.w3.org/2001/XMLSchema#string

Linjie Yan

http://www.w3.org/2001/XMLSchema#string

Shuwen Han

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P2860

Cooperative, highly enantioselective phosphinothiourea catalysis of imine-allene [3 + 2] cycloadditions.

How cinchona alkaloid-derived primary amines control asymmetric electrophilic fluorination of cyclic ketones.

Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts.

Elucidation of the active conformation of cinchona alkaloid catalyst and chemical mechanism of alcoholysis of meso anhydrides

Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts.

Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance.

The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of beta-amino acids.

Stereoselective anhydride openings.

Recent advances in enantioselective organocatalyzed anhydride desymmetrization and its application to the synthesis of valuable enantiopure compounds.

Organocatalytic enantioselective desymmetrisation.

P304

309-317

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P31

scholarly article

P356

10.3762/BJOC.14.19

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P478

http://www.w3.org/2001/XMLSchema#string

P50

Lingjun Xu

P577

2018-01-31T00:00:00Z

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P698

29507636

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P921

enantioselectivity

P932

5815282

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