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Merck
CN

804363

Sigma-Aldrich

Potassium 4-anisoyltrifluoroborate

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经验公式(希尔记法):
C8H7BF3KO2
分子量:
242.04
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

形式

powder

质量水平

SMILES字符串

O=C(B(F)(F)F)C1=CC=C(OC)C=C1.[K]

InChI

1S/C8H7BF3O2.K.H/c1-14-7-4-2-6(3-5-7)8(13)9(10,11)12;;/h2-5H,1H3;;

InChI key

VXVQBCXLJYVTDZ-UHFFFAOYSA-N

应用

Acyltrifluroborates (KAT′s) are bench, air, and moisture stable reagents for rapid, chemoselective amide bond formations with hydroxylamines. These amide bond forming reactions proceed under aqueous conditions, without the need for coupling reagents or protecting groups. This product was introduced in collaboration with the Bode Research Group.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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相关内容

The Bode Group aims to develop new reactions and reagents for the synthesis of complex molecules. The Bode Group has developed N-mesityl-substituted NHCs as organocatalysts for the catalytic generation of reactive species including activated carboxylates, homoenolates, and enolates. These novel catalysts and reactions have made possible a new generation of highly enantioselective annulations from simple starting materials under mild reaction conditions, usually at room temperature and without added reagents. Furthering the goal of designing new reagents to enable the assembly of complex molecules, the Bode group has developed SnAP reagents for the facile, one-pot conversion of aldehydes into N-unprotected, saturated N-heterocycles, including bicyclic and spirocyclic structures. These easy to handle reagents provide a simple and robust alternative to the challenging and restrictive cross-coupling methods for the functionalization of saturated N-heterocycles.

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