Facile oxidative rearrangements using hypervalent iodine reagents.
about
Thioamination of Alkenes with Hypervalent Iodine ReagentsEnantioselective diamination with novel chiral hypervalent iodine catalysts.Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine ReagentsChiral hypervalent iodine reagents: synthesis and reactivity.Hypervalent iodine(iii) fluorinations of alkenes and diazo compounds: new opportunities in fluorination chemistry.Stereoselective rearrangements with chiral hypervalent iodine reagents.A diversity oriented synthesis of natural product inspired molecular libraries.Synthesis of the Strychnos Alkaloid (-)-Strychnopivotine and Confirmation of its Absolute Configuration.Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents.One-Pot Synthesis of Allylic Sulfones, Ketosulfones, and Triflyl Allylic Alcohols from Domino Reactions of Allylic Alcohols with Sulfinic Acid under Metal-Free Conditions.Formation of the Main Cores Present in Natural Products by Tandem Additions.
P2860
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P2860
Facile oxidative rearrangements using hypervalent iodine reagents.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Facile oxidative rearrangements using hypervalent iodine reagents.
@en
Facile oxidative rearrangements using hypervalent iodine reagents.
@nl
type
label
Facile oxidative rearrangements using hypervalent iodine reagents.
@en
Facile oxidative rearrangements using hypervalent iodine reagents.
@nl
prefLabel
Facile oxidative rearrangements using hypervalent iodine reagents.
@en
Facile oxidative rearrangements using hypervalent iodine reagents.
@nl
P2093
P2860
P356
P1433
P1476
Facile oxidative rearrangements using hypervalent iodine reagents.
@en
P2093
Fateh V Singh
Julia Rehbein
Thomas Wirth
P2860
P304
P356
10.1002/OPEN.201200037
P577
2012-11-06T00:00:00Z