ChemInform Abstract: Asymmetric Synthesis of trans-2,5-Diphenylpyrrolidine: A C2-Symmetric Chiral Amine.

ChemInform ◽  
2010 ◽  
Vol 26 (32) ◽  
pp. no-no
Author(s):  
J. M. CHONG ◽  
I. S. CLARKE ◽  
I. KOCH ◽  
P. C. OLBACH ◽  
N. J. TAYLOR
Keyword(s):  
Asymmetric Synthesis ◽  
Chiral Amine

Engineering the large pocket of an (S)-selective transaminase for asymmetric synthesis of (S)-1-amino-1-phenylpropane

2021 ◽  
Author(s):  
Youyu Xie ◽  
Feng Xu ◽  
Lin Yang ◽  
He Liu ◽  
Xiangyang Xu ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Environmentally Benign ◽  
Chiral Amine ◽  
Synthesis Route

Amine transaminases offer an environmentally benign chiral amine asymmetric synthesis route.

Asymmetric Synthesis of α-Chloro-α-halo Ketones by Decarboxylative Chlorination of α-Halo-β-ketocarboxylic Acids

Synthesis ◽  
2019 ◽  
Vol 51 (23) ◽  
pp. 4385-4392 ◽  
Author(s):  
Kazumasa Kitahara ◽  
Haruna Mizutani ◽  
Seiji Iwasa ◽  
Kazutaka Shibatomi
Keyword(s):  
Asymmetric Synthesis ◽  
Chiral Amine

Chiral α-chloro-α-fluoro ketones were synthesized by enantio­selective decarboxylative chlorination of α-chloro-β-ketocarboxylic acids in the presence of a chiral amine catalyst. The reaction yielded the corresponding α-chloro-α-fluoro ketones with moderate-to-high enantioselectivity (up to 90% ee). The method was also applied to the synthesis of α-bromo-α-chloro ketones with 90% ee.

Asymmetric synthesis of trans-2,5-diphenylpyrrolidine: A C2-symmetric chiral amine

1995 ◽  
Vol 6 (2) ◽  
pp. 409-418 ◽  
Author(s):  
J Michael Chong ◽  
Ian S Clarke ◽  
Iris Koch ◽  
Peter C Olbach ◽  
Nicholas J Taylor
Keyword(s):  
Asymmetric Synthesis ◽  
Chiral Amine

Asymmetric synthesis of chiral amine in organic solvent and in-situ product recovery for process intensification: A case study

2017 ◽  
Vol 117 ◽  
pp. 97-104 ◽  
Author(s):  
Yamini Satyawali ◽  
Ehiaze Ehimen ◽  
Lieve Cauwenberghs ◽  
Miranda Maesen ◽  
Pieter Vandezande ◽  
...  
Keyword(s):  
Organic Solvent ◽  
Asymmetric Synthesis ◽  
Process Intensification ◽  
Product Recovery ◽  
Chiral Amine ◽  
In Situ Product Recovery

scholarly journals Conversion of racemic alcohols to optically pure amine precursors enabled by catalyst dynamic kinetic resolution: experiment and computation

2020 ◽  
Vol 56 (64) ◽  
pp. 9094-9097
Author(s):  
Luis Miguel Azofra ◽  
Mai Anh Tran ◽  
Viktoriia Zubar ◽  
Luigi Cavallo ◽  
Magnus Rueping ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Base Metal ◽  
Kinetic Resolution ◽  
Dynamic Kinetic Resolution ◽  
Chiral Amine ◽  
Optically Pure

An unprecedented base metal catalysed asymmetric synthesis of α-chiral amine precursors from racemic alcohols is reported.

Asymmetric synthesis of 3-substituted-2-exo-methylenecyclohexanones via 1,5-diastereoselection by using a chiral amine

1990 ◽  
Vol 55 (2) ◽  
pp. 408-410 ◽  
Author(s):  
Rui Tamura ◽  
Kenichiro Watabe ◽  
Hitoshi Katayama ◽  
Hitomi Suzuki ◽  
Yukio Yamamoto
Keyword(s):  
Asymmetric Synthesis ◽  
Chiral Amine

ChemInform Abstract: Asymmetric Synthesis of 3-Substituted 2-exo-Methylenecyclohexanones via 1,5-Diastereoselection by Using a Chiral Amine.

ChemInform ◽  
1990 ◽  
Vol 21 (24) ◽  
Author(s):  
R. TAMURA ◽  
K. WATABE ◽  
H. KATAYAMA ◽  
H. SUZUKI ◽  
Y. YAMAMOTO
Keyword(s):  
Asymmetric Synthesis ◽  
Chiral Amine
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