过渡金属催化的交叉偶联反应|Cross-Coupling using Transition Metal Catalysts-毕得医药

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过渡金属催化的交叉偶联反应是指在过渡金属配合物的催化下，RX与非过渡金属有机化合物R'M'形成碳-碳键的反应。

默认常备现货
纯度
- 请选择
- 99+%
- 99%
- 98+%
- 98%
- 97+%
- 97%
- 96+%
- 96%
- 95+%
- 95%
- 93%
- 90+%
- 90%
规格
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- 1mg
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- 5mg
- 10mg
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- 50mg
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- 250mg
- 1g
- 5g
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- 1kg

清空选项

Di-mu-chlorobis[2-[(dimethylamino)methyl]-4,6-dimethoxyphenyl-C,N]dipalladium(II): BD68246918987-71-898%; 登录 1g

Nickel(II) acetylacetonate xhydrate: BD144653120156-44-798%; 登录 1kg

Nickel(Ⅱ) acetate: BD144670373-02-495%; 登录 500g

1,3-Diisopropylimidazolinium Tetrafluoroborate: BD322186137581-18-195%; 登录 250mg

Bis(1,3-propanediaminE)copper(ii)dichloride: BD11679632270-93-295%; 登录 100mg

1,3-Di-tert-butyl-1H-imidazol-3-ium-2-ide: BD244485157197-53-098%; 登录 1g

Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0): BD3061241233717-68-495%; 登录 100mg

Hexakis(acetate)tripalladium(II): BD22525053189-26-797%; 登录 250mg

1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate: BD00813948917604-39-898% HPLC,T; 登录 1g

3,3'-Methylenebis[1-(2,6-diisopropylphenyl)-3-imidazolium bromide]: BD00811165889617-36-198%; 登录 1g

1,3-Diisopropyl-1H-imidazol-3-ium hydrogencarbonate: BD010958571372124-90-795%; 登录 250mg

Di-tert-butyl(1,1-diphenylprop-1-en-2-yl)phosphine: BD01100476384842-25-598%; 登录 1g

[(2-Dimethylamino)propyldiphenylphosphine]palladium(II) Dichloride: BD0127917985719-56-898%; 登录 250mg

Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](N,N-dimethyl-3,5-dimethoxybenzylamine)palladium(II)]: BD013446581093348-08-398+%; 登录 100mg

Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](acetanilide)palladium(II)]: BD013440331228009-69-598+%; 登录 1g

2-(Allylsulfonyl)-4-methylpyridine: BD013932642249891-89-098% +(stabilized with TBC); 登录 1g

2-(Allylsulfonyl)-5-methylpyridine: BD013593602249891-88-995% (stabilized with TBC); 登录 250mg

2-(Allylsulfonyl)-3-methylpyridine: BD013773342249891-90-398% +(stabilized with TBC); 登录 1g

2-(Allylsulfonyl)-6-methylpyridine: BD014202892249891-86-798% +(stabilized with TBC); 登录 1g

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