1,2- Versus 1,4-Asymmetric Addition of Grignard Reagents to Carbonyl Compounds

Author(s):  
Pablo Ortiz ◽  
Francesco Lanza ◽  
Syuzanna R. Harutyunyan
Synfacts ◽  
2010 ◽  
Vol 2010 (05) ◽  
pp. 0618-0618
Author(s):  
C.-S. Da ◽  
J.-R. Wang ◽  
X.-G. Yin ◽  
X.-Y. Fan ◽  
Y. Liu ◽  
...  

ChemInform ◽  
2006 ◽  
Vol 37 (29) ◽  
Author(s):  
Scott D. Kuduk ◽  
Christina Ng Di Marco ◽  
Steven M. Pitzenberger ◽  
Nancy Tsou

Synthesis ◽  
2020 ◽  
Vol 52 (13) ◽  
pp. 1855-1873
Author(s):  
Senthil Narayanaperumal ◽  
Ricardo S. Schwab ◽  
Wystan K. O. Teixeira ◽  
Danilo Yano de Albuquerque

Enantiomerically enriched diaryl, aryl heteroaryl, and dihetero­aryl alcohols are an important family of compounds known for their biological properties. Moreover, these molecules are highly privileged scaffolds used as building blocks for the synthesis of pharmaceutically relevant products. This short review provides background on the enantioselective arylation and heteroarylation of carbonyl compounds, as well as, the most significant improvements in this field with special emphasis on the application of organometallic reagents.1 Introduction2 Background on the Enantioselective Synthesis of Diaryl, Aryl Heteroaryl, and Diheteroaryl Alcohols3 Organozinc Reagents4 Organolithium Reagents5 Grignard Reagents6 Organoaluminum Reagents7 Organotitanium Reagents8 Organobismuth Reagents9 Miscellaneous10 Conclusion


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