Catalytic Asymmetric Construction of α-Quaternary Cyclopentanones and Its Application to the Syntheses of (-)-1,14-Herbertenediol and (-)-Aphanorphine.

about

Catalytic Asymmetric Construction of α-Quaternary Cyclopentanones and Its Application to the Syntheses of (-)-1,14-Herbertenediol and (-)-Aphanorphine.

Item

http://www.wikidata.org/entity/Q50933333

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Catalytic Asymmetric Construct ...... tenediol and (-)-Aphanorphine.

@en

Catalytic Asymmetric Construct ...... tenediol and (-)-Aphanorphine.

@nl

type

Item

label

Catalytic Asymmetric Construct ...... tenediol and (-)-Aphanorphine.

@en

Catalytic Asymmetric Construct ...... tenediol and (-)-Aphanorphine.

@nl

prefLabel

Catalytic Asymmetric Construct ...... tenediol and (-)-Aphanorphine.

@en

Catalytic Asymmetric Construct ...... tenediol and (-)-Aphanorphine.

@nl

P1476

Catalytic Asymmetric Construct ...... tenediol and (-)-Aphanorphine.

@en

P2093

Dao-Yong Zhu

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

Fu-Min Zhang

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

Ming-Hui Xu

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

Shao-Hua Wang

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

Yong-Qiang Tu

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

P2860

Novel neurotrophic isocuparane-type sesquiterpene dimers, mastigophorenes A, B, C and D, isolated from the liverwort Mastigophora diclados

Semipinacol Rearrangement in Natural Product Synthesis

The Construction of All-Carbon Quaternary Stereocenters by Use of Pd-Catalyzed Asymmetric Allylic Alkylation Reactions in Total Synthesis

Chiral anion-mediated asymmetric ring opening of meso-aziridinium and episulfonium ions.

Asymmetric catalysis for the construction of quaternary carbon centres: nucleophilic addition on ketones and ketimines.

Catalytic asymmetric synthesis of all-carbon quaternary stereocenters

Bioactive compounds from liverworts: Inhibition of lipopolysaccharide-induced inducible NOS mRNA in RAW 264.7 cells by herbertenoids and cuparenoids.

Ring-contraction strategy for the practical, scalable, catalytic asymmetric synthesis of versatile γ-quaternary acylcyclopentenes.

An improved catalyst for the asymmetric arylation of ketone enolates.

The rearrangement of 2,3-epoxysulfonates and its application to natural products syntheses: formal synthesis of (-)-aphanorphine and total syntheses of (-)-alpha-herbertenol and (-)-herbertenediol.

P304

15502-15505

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

P31

scholarly article

P356

10.1002/CHEM.201502700

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

P577

2015-09-04T00:00:00Z

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

P698

26387785

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