Cu-Catalyzed hydrophosphorylative ring opening of propargyl epoxides: highly selective access to 4-phosphoryl 2,3-allenols.

about

Fifty Years of (Benz)oxaphospholene Chemistry.Copper-catalyzed silylation reactions of propargyl epoxides: easy access to 2,3-allenols and stereodefined alkenes.

P2860

Q47802032-33490CB5-4A3E-451C-9484-F254B72D01DD Q54212932-6E4A980A-799F-4516-A47C-75A64E1C15C8

P2860

Cu-Catalyzed hydrophosphorylative ring opening of propargyl epoxides: highly selective access to 4-phosphoryl 2,3-allenols.

Item

http://www.wikidata.org/entity/Q51144782

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

Cu-Catalyzed hydrophosphorylat ...... to 4-phosphoryl 2,3-allenols.

@en

Cu-Catalyzed hydrophosphorylat ...... to 4-phosphoryl 2,3-allenols.

@nl

type

Item

label

Cu-Catalyzed hydrophosphorylat ...... to 4-phosphoryl 2,3-allenols.

@en

Cu-Catalyzed hydrophosphorylat ...... to 4-phosphoryl 2,3-allenols.

@nl

prefLabel

Cu-Catalyzed hydrophosphorylat ...... to 4-phosphoryl 2,3-allenols.

@en

Cu-Catalyzed hydrophosphorylat ...... to 4-phosphoryl 2,3-allenols.

@nl

P1476

Cu-Catalyzed hydrophosphorylat ...... to 4-phosphoryl 2,3-allenols.

@en

P2093

Haipeng Zhao

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

Jianlin Yang

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

Li-Biao Han

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

Lixiong Zhang

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

Ruwei Shen

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

Yu Feng

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

P2860

Synthesis and properties of allenic natural products and pharmaceuticals.

Organo-manganese η2-auxiliary directed reactions: a diastereoselective approach to 2,3-allenols.

Catalytic Borylative Opening of Propargyl Cyclopropane, Epoxide, Aziridine, and Oxetane Substrates: Ligand Controlled Synthesis of Allenyl Boronates and Alkenyl Diboronates.

Phenylsulfonyl ene-allenes as efficient precursors to bicyclic systems via intramolecular [2 + 2]-cycloaddition reactions.

Palladium pincer complex catalyzed stannyl and silyl transfer to propargylic substrates: synthetic scope and mechanism.

Stereoselective synthesis of syn-configured alpha-allenols by rhodium-catalyzed reaction of alkynyl oxiranes with arylboronic acids.

An efficient synthesis of carbazoles from PtCl(2)-catalyzed cyclization of 1-(indol-2-yl)-2,3-allenols.

Efficient synthesis of 3-chloromethyl-2(5H)-furanones and 3-chloromethyl-5,6-dihydropyran-2-ones via the PdCl2-catalyzed chlorocyclocarbonylation of 2,3- or 3,4-allenols.

Synthesis of diversely substituted 2-(furan-3-yl)acetates from allenols through cascade carbonylations.

C-P bond-forming reactions via C-O/P-H cross-coupling catalyzed by nickel.

P304

11959-11962

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

P31

scholarly article

P356

10.1039/C6CC05428E

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

2016-09-01T00:00:00Z

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

P698

27709204

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

Cu-Catalyzed hydrophosphorylative ring opening of propargyl epoxides: highly selective access to 4-phosphoryl 2,3-allenols.

about

P2860

P2860

Cu-Catalyzed hydrophosphorylative ring opening of propargyl epoxides: highly selective access to 4-phosphoryl 2,3-allenols.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698