Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

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Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

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http://www.wikidata.org/entity/Q52314989

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2018 nî lūn-bûn

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2018年の論文

@ja

2018年学术文章

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2018年学术文章

@zh

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年學術文章

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2018年學術文章

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name

Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

@en

Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

@nl

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Item

label

Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

@en

Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

@nl

prefLabel

Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

@en

Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides.

@nl

P1476

Stereoselective photoredox ring-opening polymerization of O-carboxyanhydrides

@en

P2093

Dong Guo

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

Lei Yang

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

Wei Huang

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

Yongliang Zhong

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

P2860

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

Remarkable stereocontrol in the polymerization of racemic lactide using aluminum initiators supported by tetradentate aminophenoxide ligands.

Allosteric supramolecular triple-layer catalysts.

Kinetic resolution of racemic alpha-olefins with ansa-zirconocene polymerization catalysts: Enantiomorphic site vs. chain end control

Crystalline CO2-based polycarbonates prepared from racemic catalyst through intramolecularly interlocked assembly.

Synthesis of water-soluble poly(α-hydroxy acids) from living ring-opening polymerization of O-benzyl-L-serine carboxyanhydrides.

Drug-initiated ring-opening polymerization of O-carboxyanhydrides for the preparation of anticancer drug-poly(O-carboxyanhydride) nanoconjugates

Stereocontrolled ring-opening polymerization of cyclic esters: synthesis of new polyester microstructures.

Stereocontrolled ring-opening polymerisation of lactide.

Beyond stereoselectivity, switchable catalysis: some of the last frontier challenges in ring-opening polymerization of cyclic esters.

P2888

s41467-018-03879-5

P304

1559

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P31

scholarly article

P356

10.1038/S41467-018-03879-5

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

P407

English

P433

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

P478

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

P50

P577

2018-04-19T00:00:00Z

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P698

29674720

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P921

stereoselectivity

P932

5908805

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