about
CO/O2 assisted oxidative carbon-carbon and carbon-heteroatom bond cleavage for the synthesis of oxosulfonates from DMSO and olefinsSynthesis of a Sulfonimidamide-Based Analog of Tasisulam and Its Biological Evaluation in the Melanoma Cell Lines SKMel23 and A375.A New, Practical One-Pot Synthesis of Unprotected Sulfonimidamides by Transfer of Electrophilic NH to Sulfinamides.SuFEx Chemistry of Thionyl Tetrafluoride (SOF4 ) with Organolithium Nucleophiles: Synthesis of Sulfonimidoyl Fluorides, Sulfoximines, Sulfonimidamides, and Sulfonimidates.Mechanistic investigation of the NH-sulfoximination of sulfide. Evidence for λ6-sulfanenitrile intermediates.Exploration of Novel Chemical Space: Synthesis and in vitro Evaluation of N-Functionalized Tertiary Sulfonimidamides.
P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
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
@yue
2016年學術文章
@zh-hant
name
Copper-Catalyzed S-C/S-N Bond Interconversions.
@en
Copper-Catalyzed S-C/S-N Bond Interconversions.
@nl
type
label
Copper-Catalyzed S-C/S-N Bond Interconversions.
@en
Copper-Catalyzed S-C/S-N Bond Interconversions.
@nl
prefLabel
Copper-Catalyzed S-C/S-N Bond Interconversions.
@en
Copper-Catalyzed S-C/S-N Bond Interconversions.
@nl
P2860
P356
P1476
Copper-Catalyzed S-C/S-N Bond Interconversions.
@en
P2093
P2860
P304
P356
10.1002/CHEM.201600661
P407
P577
2016-02-19T00:00:00Z