Highly Regio- and Enantioselective Formal [3 + 2]-Annulation of Indoles with Electrophilic Enol Carbene Intermediates.
about
Cycloaddition reactions of enoldiazo compounds.Catalytic Asymmetric [3+1]-Cycloaddition Reaction of Ylides with Electrophilic Metallo-enolcarbene Intermediates.A Stereoselective [3+1] Ring Expansion for the Synthesis of Highly Substituted Methylene Azetidines.Gold-catalyzed stereoselective dearomatization/metal-free aerobic oxidation: access to 3-substituted indolines/oxindoles.Blue light-promoted photolysis of aryldiazoacetates.
P2860
Highly Regio- and Enantioselective Formal [3 + 2]-Annulation of Indoles with Electrophilic Enol Carbene Intermediates.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
@wuu
2016年学术文章
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2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
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2016年學術文章
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name
Highly Regio- and Enantioselec ...... ic Enol Carbene Intermediates.
@en
Highly Regio- and Enantioselec ...... ic Enol Carbene Intermediates.
@nl
type
label
Highly Regio- and Enantioselec ...... ic Enol Carbene Intermediates.
@en
Highly Regio- and Enantioselec ...... ic Enol Carbene Intermediates.
@nl
prefLabel
Highly Regio- and Enantioselec ...... ic Enol Carbene Intermediates.
@en
Highly Regio- and Enantioselec ...... ic Enol Carbene Intermediates.
@nl
P50
P1433
P1476
Highly Regio- and Enantioselec ...... lic Enol Carbene Intermediates
@en
P2093
Hadi Arman
Michael P Doyle
P304
P356
10.1021/ACS.ORGLETT.6B02192
P407
P577
2016-09-02T00:00:00Z