Haloalkynes: a powerful and versatile building block in organic synthesis.

Haloalkynes: a powerful and versatile building block in organic synthesis.

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http://www.wikidata.org/entity/Q47592590
Calcium Carbide: A Unique Reagent for Organic Synthesis and Nanotechnology.Conversion of Triple Bonds into Single Bonds in a Domino Carbopalladation with Norbornene.A General Nickel-Catalyzed Method for C-H Bond Alkynylation of Heteroarenes Through Chelation Assistance.Metal-free, Regio-, and Stereo-Controlled Hydrochlorination and Hydrobromination of Ynones and Ynamides.N-Heterocyclic carbene palladium-catalyzed cascade annulation/alkynylation of 2-alkynylanilines with terminal alkynes.MnO2 -Promoted Oxidative Radical Sulfonylation of Haloalkynes with Sulfonyl Hydrazides: C(sp)-S Bond Formation towards Alkynyl Sulfones.Huanfeng Jiang.Cu-catalyzed Cascade Cyclization of Isothiocyanates, Alkynes, and Diaryliodonium Salts: Access to Diversely Functionalized Quinolines.Reductive Decarboxylative Alkynylation of N-Hydroxyphthalimide Esters with Bromoalkynes.Acetylenic scaffolding with subphthalocyanines - synthetic scope and elucidation of electronic interactions in dimeric structures.Sunlight-Driven Decarboxylative Alkynylation of α-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones.MnO2-promoted carboesterification of alkenes with anhydrides: a facile approach to γ-lactones.Highly Efficient and Stereoselective Thioallylation of Alkynes: Possible Gold Redox Catalysis with No Need of a Strong Oxidant.Intermolecular asymmetric carboesterification of alkenes by using chiral amine auxiliaries under O2: synthesis of enantioenriched α-methylene-γ-lactones through chloropalladation of alkynes.Synthesis of 3-bromosubstituted pyrroles via palladium-catalyzed intermolecular oxidative cyclization of bromoalkynes with N-allylamines.Regioselective Synthesis of Polyheterohalogenated Naphthalenes via the Benzannulation of Haloalkynes.Hydrogen-Bonding-Assisted Brønsted Acid and Gold Catalysis: Access to Both ()- and ()-1,2-Haloalkenes via Hydrochlorination of Haloalkynes
P2860

Haloalkynes: a powerful and versatile building block in organic synthesis.

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http://www.wikidata.org/entity/Q47592590
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2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
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2014年学术文章
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2014年學術文章
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2014年學術文章
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name
Haloalkynes: a powerful and versatile building block in organic synthesis.
@en
Haloalkynes: a powerful and versatile building block in organic synthesis.
@nl
type
label
Haloalkynes: a powerful and versatile building block in organic synthesis.
@en
Haloalkynes: a powerful and versatile building block in organic synthesis.
@nl
prefLabel
Haloalkynes: a powerful and versatile building block in organic synthesis.
@en
Haloalkynes: a powerful and versatile building block in organic synthesis.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P577
P698
P356
P1433
P1476
Haloalkynes: a powerful and versatile building block in organic synthesis.
@en
P2093
P304
P31
P356
P407
P433
P478
P577
P698