Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis.
about
Direct Observation of Intermediates Involved in the Interruption of the Bischler-Napieralski ReactionMetal-Free C-H Alkyliminylation and Acylation of Alkenes with Secondary AmidesMechanistic 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.
P2860
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P2860
Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis.
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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name
Direct room-temperature lacton ...... amide strategy" for synthesis.
@en
Direct room-temperature lacton ...... amide strategy" for synthesis.
@nl
type
label
Direct room-temperature lacton ...... amide strategy" for synthesis.
@en
Direct room-temperature lacton ...... amide strategy" for synthesis.
@nl
prefLabel
Direct room-temperature lacton ...... amide strategy" for synthesis.
@en
Direct room-temperature lacton ...... amide strategy" for synthesis.
@nl
P2093
P2860
P356
P1476
Direct room-temperature lacton ...... "amide strategy" for synthesis
@en
P2093
Claire Madelaine
Desislava Petkova
Viviana Valerio
P2860
P304
P356
10.1002/CHEM.201203906
P407
P50
P577
2013-01-10T00:00:00Z