Enantioselective Synthesis of 1,3-Dioxygen-substituted Chiral Building Blocks

Synlett ◽  
1994 ◽  
Vol 1994 (03) ◽  
pp. 199-200 ◽  
Author(s):  
Chris H. Senanayake ◽  
Robert D. Larsen ◽  
Timothy J. Bill ◽  
Ji Liu ◽  
Edward G. Corley ◽  
...  
2019 ◽  
Author(s):  
Ming Shang ◽  
Karla S. Feu ◽  
Julien C. Vantourout ◽  
Lisa M. Barton ◽  
Heather L. Osswald ◽  
...  

<div> <div> <div> <p>The union of two powerful transformations, directed C–H activation and decarboxylative cross-coupling, for the enantioselective synthesis of vicinally functionalized alkyl, carbocyclic, and heterocyclic compounds is described. Starting from simple carboxylic acid building blocks, this modular sequence exploits the residual directing group to access more than 50 scaffolds that would be otherwise extremely difficult to prepare. The tactical use of these two transformations accomplishes a formal vicinal difunctionalization of carbon centers in a way that is modular and thus amenable to rapid diversity incorporation. A simplification of routes to known preclinical drug candidates is presented along with the rapid diversification of an antimalarial compound series. </p> </div> </div> </div>


ChemInform ◽  
2006 ◽  
Vol 37 (33) ◽  
Author(s):  
Alejandro Baeza ◽  
Jesus Casas ◽  
Carmen Najera ◽  
Jose M. Sansano ◽  
Jose M. Saa

2021 ◽  
Author(s):  
Zeynep Dilşad Susam ◽  
Merve Bozdemir ◽  
Gülsüm Gündoğdu ◽  
Cihangir Tanyeli

Asymmetric organocatalytic domino type Michael-SN2 reactions give access to enantiomerically enriched dihydrofuran derivatives that can be used as valuable chiral building blocks. A variety of α-bromonitroalkenes and 1,3-dicarbonyl compounds were...


2020 ◽  
Vol 56 (43) ◽  
pp. 5823-5826
Author(s):  
Marta Velázquez ◽  
Saúl Alberca ◽  
Javier Iglesias-Sigüenza ◽  
Rosario Fernández ◽  
José M. Lassaletta ◽  
...  

Asymmetric 1,2-addition of aryl boronic acids to N-carbamoyl (Cbz and Fmoc) protected glyoxylate-derived hydrazones affords α-aryl α-hydrazino esters/amides, key building blocks en route to artificial peptides.


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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