A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles.

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Synthesis of 2-fluoro-2-pyrrolines via tandem reaction of α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates.Synthesis of 3-bromosubstituted pyrroles via palladium-catalyzed intermolecular oxidative cyclization of bromoalkynes with N-allylamines.

P2860

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P2860

A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles.

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http://www.wikidata.org/entity/Q53090421

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

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2013年學術文章

@zh-hant

name

A novel reaction of gem-difluo ...... s leading to 2-fluoropyrroles.

@en

A novel reaction of gem-difluo ...... s leading to 2-fluoropyrroles.

@nl

type

Item

label

A novel reaction of gem-difluo ...... s leading to 2-fluoropyrroles.

@en

A novel reaction of gem-difluo ...... s leading to 2-fluoropyrroles.

@nl

prefLabel

A novel reaction of gem-difluo ...... s leading to 2-fluoropyrroles.

@en

A novel reaction of gem-difluo ...... s leading to 2-fluoropyrroles.

@nl

P1476

A novel reaction of gem-difluo ...... s leading to 2-fluoropyrroles.

@en

P2093

Ji-Chang Xiao

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

Qing-Yun Chen

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

Tang-Po Yang

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

P2860

Pyrrolo[1,2-b]pyridazin-2-ones as potent inhibitors of HCV NS5B polymerase

A powerful new strategy for diversity-oriented synthesis of pyrroles from donor-acceptor cyclopropanes and nitriles.

A novel synthesis of 7-aryl-8-fluoro-pyrrolo[1,2-a]pyrimid-4-ones as potent, stable GnRH receptor antagonists.

Methylene-gem-difluorocyclopropane analogues of nucleosides: synthesis, cyclopropene-methylenecyclopropane rearrangement, and biological activity.

Trapping a diradical transition state by mechanochemical polymer extension.

Synthesis of tetrahydropyrans from propargyl alcohols and 1,1-cyclopropanediesters: a one-pot ring-opening/Conia-ene protocol.

Formal [3 + 2] cycloadditions of donor-acceptor cyclopropanes and nitriles.

Stereochemistry of C-6 nucleophilic displacements on 1,1-difluorocyclopropyldibenzosuberanyl substrates. An improved synthesis of multidrug resistance modulator LY335979 trihydrochloride.

Ionic liquid, surrogate hydrogen bromide reagent for ring opening of cyclopropyl ketones.

New synthesis of 3-fluoropyrroles.

P304

9833-9835

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P31

scholarly article

P356

10.1039/C3CC45456H

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English

P433

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

P478

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

P50

Jin-Hong Lin

P577

2013-10-01T00:00:00Z

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

P698

24030730

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

A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles.

about

P2860

P2860

A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698