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Merck
CN

900542

Sigma-Aldrich

(2S)-2-Phenyl-3,4-dihydro-2H-pyrimido[2,1-b][1,3]benzothiazole

95%

别名:

Birman (S)-HBTM Resolution Catalyst

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About This Item

经验公式(希尔记法):
C16H14N2S
分子量:
266.36
MDL编号:
UNSPSC代码:
12161600
NACRES:
NA.22

质量水平

方案

95%

表单

powder or chunks

mp

125 °C

官能团

phenyl
thioether

储存温度

2-8°C

SMILES字符串

C12=CC=CC=C1SC3=N[C@H](C4=CC=CC=C4)CCN23

InChI

1S/C16H14N2S/c1-2-6-12(7-3-1)13-10-11-18-14-8-4-5-9-15(14)19-16(18)17-13/h1-9,13H,10-11H2/t13-/m0/s1

InChI key

ZMYZJAQMQBHNLH-ZDUSSCGKSA-N

应用

Organocatalyst for the kinetic resolution of secondary alcohols by acylation with anhydrides.

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象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Ximin Li et al.
The Journal of organic chemistry, 77(4), 1722-1737 (2012-01-31)
Kinetic resolution of racemic alcohols has been traditionally achieved via enzymatic enantioselective esterification and ester hydrolysis. However, there has long been considerable interest in devising nonenzymatic alternative methods for this transformation. Amidine-based catalysts (ABCs), a new class of enantioselective acyl

相关内容

The main focus of research in the Birman group is on the de novo design of asymmetric catalysts and reagents. As part of this effort, they have developed Amidine-Based Catalysts, or ABCs, and demonstrated their high enantioselectivity in many asymmetric acyl transfer reactions. The versatility, accessibility, and ease of structural modification of ABCs have attracted the interest of a number of other research groups worldwide, which has led to further expansion of their synthetic utility.

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