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Merck
모든 사진(1)

주요 문서

905798

Sigma-Aldrich

Dimethylsulfoxonium-(isobutanoyl)methylide

≥95%

동의어(들):

1-(Dimethyl(oxo)-sulfaneylidene)-3-methylbutan-2-one

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About This Item

실험식(Hill 표기법):
C7H14O2S
CAS Number:
Molecular Weight:
162.25
UNSPSC 코드:
12352101

분석

≥95%

양식

solid

반응 적합성

reaction type: C-C Bond Formation

mp

140-144 °C

작용기

ketone
sulfoxide

저장 온도

−20°C

SMILES string

O=C(C(C)C)C=S(C)(C)=O

일반 설명

Sulfoxonium ylides are highly stable carbene precursors, serving as a safer alternative to diazo compounds as they that do not generate gases as byproducts. Sulfoxonium ylides have been shown to be effective in a wide array of transition metal catalyzed C-H functionalization and coupling reactions.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Alicia M Phelps et al.
The Journal of organic chemistry, 81(10), 4158-4169 (2016-04-23)
An iridium-catalyzed method was developed for the synthesis of imidazo-fused pyrrolopyrazines. The presence or absence of a nitrogenated ligand controlled the outcome of the reaction, leading to simple β-keto amine products in the absence of added ligand and the cyclized
Shuying Ji et al.
Organic letters, 20(18), 5981-5984 (2018-09-13)
A Cp*Co(III)-catalyzed C-H bond functionalization of a range of arenes by employing sulfoxonium ylides as carbene precursors instead of diazo compounds and other carbene precursors has been established. This reaction is highly efficient without any additive, possesses high step and
Panjie Hu et al.
Organic letters, 20(8), 2160-2163 (2018-04-03)
Rh(III)-catalyzed cascade C-H activation of benzoylacetonitriles and annulation with sulfoxonium ylides was realized, leading to selective synthesis of naphthols, 2,3-dihydronaphtho[1,8- bc]pyrans, and naphtho[1,8- bc]pyrans. This step-economic reaction proceeded efficiently under mild and redox-neutral conditions via multiple C-H activations.

관련 콘텐츠

Ketosulfoxonium ylides serve as versatile carbene equivalents for large-scale reactions, releasing dimethyl sulfoxide biproducts.

Ellman group developed electron-rich phosphine ligands for C-H functionalization and tert-Butanesulfinamide for asymmetric amine synthesis.

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