Asymmetric Aldol Addition by Oligopeptide Immobilized on Magnetic Particles through an Ionic Liquids Spacer

2008 ◽  
Vol 47 (23) ◽  
pp. 9628-9635 ◽  
Author(s):  
Yangyang Jiang ◽  
Chen Guo ◽  
Hansong Xia ◽  
Iram Mahmood ◽  
Huizhou Liu
2007 ◽  
Vol 349 (11-12) ◽  
pp. 2061-2065 ◽  
Author(s):  
Marco Lombardo ◽  
Filippo Pasi ◽  
Srinivasan Easwar ◽  
Claudio Trombini

Synthesis ◽  
2017 ◽  
Vol 50 (02) ◽  
pp. 211-226 ◽  
Author(s):  
Perla Ramesh ◽  
Devatha Suman ◽  
Koti Reddy

Baclofen is an antispastic drug used as a muscle relaxant in the treatment of the paroxysmal pain of trigeminal neuralgia, spasticity of the spinal cord and cerebral origin. Baclofen resides biological activity exclusively in its (R)-(–)-enantiomer. In this review, various asymmetric synthetic strategies for (R)-(–)-baclofen are described.1 Introduction2 Resolution Synthetic Approaches2.1 Chemical Resolution2.2 Biocatalytic Resolution3 Asymmetric Desymmetrization3.1 Catalytic Enantioselective Desymmetrization3.2 Enzymatic Desymmetrization4 Chiral Auxiliary Induced Asymmetric Synthesis4.1 Asymmetric Michael Addition4.2 Asymmetric Aldol Addition4.3 Asymmetric Nucleophilic Substitution5 Asymmetric Reduction5.1 Catalytic Asymmetric Hydrogenation5.2 Bioreduction6 Catalytic Asymmetric Conjugate Addition7 Conclusion


ChemInform ◽  
2009 ◽  
Vol 40 (10) ◽  
Author(s):  
Marco Lombardo ◽  
Srinivasan Easwar ◽  
Filippo Pasi ◽  
Claudio Trombini ◽  
Dilip D. Dhavale

Tetrahedron ◽  
2016 ◽  
Vol 72 (35) ◽  
pp. 5414-5419 ◽  
Author(s):  
Rosaria Villano ◽  
Maria Rosaria Acocella ◽  
Arrigo Scettri

ChemInform ◽  
2010 ◽  
Vol 28 (51) ◽  
pp. no-no
Author(s):  
K. ISEKI ◽  
Y. KUROKI ◽  
D. ASADA ◽  
M. TAKAHASHI ◽  
S. KISHIMOTO ◽  
...  

Synfacts ◽  
2011 ◽  
Vol 2011 (02) ◽  
pp. 0177-0177
Author(s):  
S. Denmark ◽  
T. Wilson

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 648
Author(s):  
Yu-Hao Zhou ◽  
Yu-Zu Zhang ◽  
Zhu-Lian Wu ◽  
Tian Cai ◽  
Wei Wen ◽  
...  

A highly efficient quinine-derived primary-amine-catalyzed asymmetric aldol addition of hydroxyacetone to arylglyoxals is described. Structurally diverse anti-2,3-dihydroxy-1,4-diones were generated in high yields, with good diastereoselectivities and enantioselectivities.


ChemInform ◽  
2007 ◽  
Vol 38 (52) ◽  
Author(s):  
Marco Lombardo ◽  
Filippo Pasi ◽  
Srinivasan Easwar ◽  
Claudio Trombini

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