A highly stereoselective Diels-Alder cycloaddition of enones with chiral cyclic 2-amidodienes derived from allenamides.
about
A highly regio- and stereoselective synthesis of α-fluorinated imides via fluorination of chiral enamidesStereoselective synthesis of isoquinuclidines through an aza-[4 + 2] cycloaddition of chiral cyclic 2-amidodienes.A Silver(I)-Catalyzed Intramolecular Ficini's [2 + 2] Cycloaddition Employing Ynamides.Copper-catalyzed skeletal rearrangements of O-propargylic oximes via cleavage of a carbon-oxygen bond.An unexpected double Diels-Alder reaction of (E)-2-bromo-4-aryl-1,3-pentadiene involving [1,5]-hydrogen migration and HBr elimination: synthesis of bicyclo[2.2.2]octene derivatives.Facile Synthesis of 3-Amido-Dienynes via a Tandem α-Propargylation-Isomerization of Chiral Allenamides and their Applications in Diels-Alder Cycloadditions.
P2860
A highly stereoselective Diels-Alder cycloaddition of enones with chiral cyclic 2-amidodienes derived from allenamides.
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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name
A highly stereoselective Diels ...... enes derived from allenamides.
@en
A highly stereoselective Diels ...... enes derived from allenamides.
@nl
type
label
A highly stereoselective Diels ...... enes derived from allenamides.
@en
A highly stereoselective Diels ...... enes derived from allenamides.
@nl
prefLabel
A highly stereoselective Diels ...... enes derived from allenamides.
@en
A highly stereoselective Diels ...... enes derived from allenamides.
@nl
P2093
P2860
P356
P1433
P1476
A highly stereoselective Diels ...... enes derived from allenamides.
@en
P2093
Li-Chao Fang
Richard P Hsung
William R Presser
Zhi-Xiong Ma
P2860
P304
P356
10.1021/OL402254P
P407
P577
2013-09-03T00:00:00Z