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Merck
CN

906719

Pyrylium tetrafluoroborate

≥95%

别名:

Pyry-BF4

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关于此项目

经验公式(希尔记法):
C5H5BF4O
化学文摘社编号:
分子量:
167.90
MDL number:
UNSPSC Code:
12352107
NACRES:
NA.22
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InChI key

SJNICXIZTGPXAU-UHFFFAOYSA-N

InChI

1S/C5H5O.BF4/c1-2-4-6-5-3-1;2-1(3,4)5/h1-5H;/q+1;-1

SMILES string

[B-](F)(F)(F)F.[o+]1ccccc1

assay

≥95%

form

powder

storage temp.

2-8°C

Application

Pyrylium tetrafluoroborate is used for the functionalization of heterocyclic amines, activating them for nucleophilic substitution. As demonstrated by the Cornella lab, the intermediate pyridinium salts can react with a vast array of nucelophiles to form new C-N, C-O, and C-S bonds, making pyrylium tetrafluoroborate a valuable reagent for late-stage functionalization.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Daniel Moser et al.
Angewandte Chemie (International ed. in English), 57(34), 11035-11039 (2018-07-04)
The functionalization of aminoheterocycles by using a pyrylium tetrafluoroborate reagent (Pyry-BF4 ) is presented. This reagent efficiently condenses with a great variety of heterocyclic amines and primes the C-N bond for nucleophilic aromatic substitution. More than 60 examples for the

相关内容

The main focus of the Cornella research group is the development of rapid, practical and efficient methodologies for organic synthesis. In addition to efficiency and practicality, the group is highly interested in discovering new reactivity with the aim of unveiling novel transformations. More specifically, on the fundamental understanding and application of catalytic processes and the development of simple reagents. These two approaches have enormous potential and impact across the chemical sciences.

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