Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis. - Wikidata - wikimedia - TriplyDB

Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis.

Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis.

http://www.wikidata.org/entity/Q51838871

about

Direct Observation of Intermediates Involved in the Interruption of the Bischler-Napieralski Reaction Metal-Free C-H Alkyliminylation and Acylation of Alkenes with Secondary Amides Mechanistic Pathways in Amide Activation: Flexible Synthesis of Oxazoles and Imidazoles.Synthesis of γ-pyrones via decarboxylative condensation of β-ketoacids.General one-pot reductive gem-bis-alkylation of tertiary lactams/amides: rapid construction of 1-azaspirocycles and formal total synthesis of (±)-cephalotaxine.Ru-catalyzed asymmetric hydrogenation of δ-keto Weinreb amides: enantioselective synthesis of (+)-Centrolobine.MnO2-promoted carboesterification of alkenes with anhydrides: a facile approach to γ-lactones.Direct reductive coupling of secondary amides: chemoselective formation of vicinal diamines and vicinal amino alcohols.Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones.Unusual mechanisms in Claisen rearrangements: an ionic fragmentation leading to a meta-selective rearrangement.

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P2860

Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis.

http://www.wikidata.org/entity/Q51838871

description

2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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name

Direct room-temperature lacton ...... amide strategy" for synthesis.

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Direct room-temperature lacton ...... amide strategy" for synthesis.

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type

label

Direct room-temperature lacton ...... amide strategy" for synthesis.

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Direct room-temperature lacton ...... amide strategy" for synthesis.

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prefLabel

Direct room-temperature lacton ...... amide strategy" for synthesis.

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Direct room-temperature lacton ...... amide strategy" for synthesis.

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Chemistry: A European Journal

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Direct room-temperature lacton ...... "amide strategy" for synthesis

@en

P2093

Claire Madelaine

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Desislava Petkova

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Viviana Valerio

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P2860

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

Twisted amide reduction under Wolff-Kishner conditions: synthesis of a benzo-1-aza-adamantane derivative.

Macrolactonizations in the total synthesis of natural products.

Asymmetric total synthesis of soraphen A: a flexible alkyne strategy

Protecting-group-free synthesis as an opportunity for invention.

Aiming for the ideal synthesis.

Versatile one-pot reductive alkylation of lactams/amides via amide activation: application to the concise syntheses of bioactive alkaloids (±)-bgugaine, (±)-coniine, (+)-preussin, and (-)-cassine.

Controlled and chemoselective reduction of secondary amides.

Asymmetric, protecting-group-free total synthesis of (-)-englerin A.

Macrolactonization via hydrocarbon oxidation.

P304

2606-2610

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scholarly article

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10.1002/CHEM.201203906

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8

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19

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2013-01-10T00:00:00Z

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23307662

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