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Documenti fondamentali

ALD00444

Sigma-Aldrich

Late Stage Functionalization Toolkit

Sinonimo/i:

Baran Late-Stage Functionalization Kit, LSF Toolkit featuring Baran Diversinates™

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About This Item

Codice UNSPSC:
41116155
NACRES:
NA.22

Temperatura di conservazione

2-8°C

Applicazioni

The Baran Late-Stage Toolkit is a convenient collection of 12 highly innovative reagents that are highly effective in the diversification of complex molecules. The contents in the box are 11 Baran Diversinates™ and one vial of Palau′Chlor® in amounts of 100 mg each. For obtaining larger amounts of any desired kit component, see the kit component table at the bottom of the page.

Useful Topics:
Late Stage Functionalization

Baran Group – Professor Product Portal

Palau′Chlor
Diversinates

Note legali

Diversinates is a trademark of Sigma-Aldrich Co. LLC
Palau′Chlor is a registered trademark of Merck KGaA, Darmstadt, Germany

I componenti del kit sono disponibili anche separatamente

N° Catalogo
Descrizione
SDS
  • 745480Zinc isopropylsulfinate, 95%SDS
  • 745405Sodium 1,1-difluoroethanesulfinateSDS
  • 745499Zinc trifluoroethanesulfinateSDS
  • 767840Zinc difluoromethanesulfinate, 95%SDS
  • 771406Zinc trifluoromethanesulfinateSDS
  • ALD00288Sodium tert-butylsulfinateSDS
  • ALD00290Sodium 2,2-dimethylpropylsulfinateSDS
  • 792454Palau′Chlor®, 95%SDS
  • 790184Sodium 1-(trifluoromethyl)cyclopropanesulfinateSDS
  • 790796Zinc benzylsulfinateSDS
  • ALD00230Sodium 4,4-difluorocyclohexanesulfinateSDS
  • ALD00232Sodium tetrahydropyransulfinateSDS
Vedi tutto (12)

Avvertenze

Danger

Indicazioni di pericolo

H314,H335,H410

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

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Certificati d'analisi (COA)

Lot/Batch Number

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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

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A C?H Methylation Reaction of Heteroarenes Inspired by Radical SAM Methyl Transferase.
Gui J, et al.
Journal of the American Chemical Society, 136, 4853-4856 (2014)
Simple Sulfinate Synthesis Enables C-H Trifluoromethylcyclopropanation
Gianatassio R, et al.
Angewandte Chemie (International Edition in English), 53, 9851-9855 (2014)
Radical C?H Functionalization of Heteroarenes under Electrochemical Control.
O'Brien, et al.
Angewandte Chemie (International Edition in English), 53, 11868-11871 (2014)
Palau'chlor: A Practical and Reactive Chlorinating Reagent
Rodriguez RA, et al.
Journal of the American Chemical Society, 136, 6908-6911 (2014)
Yuta Fujiwara et al.
Journal of the American Chemical Society, 134(3), 1494-1497 (2012-01-11)
Molecular scaffolds containing alkylfluorine substituents are desired in many areas of chemical research from materials to pharmaceuticals. Herein, we report the invention of a new reagent (Zn(SO(2)CF(2)H)(2), DFMS) for the innate difluoromethylation of organic substrates via a radical process. This
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