ChemInform Abstract: An Organo-NHC Catalyzed Domino Addition Approach for the Selective Synthesis of 5-Butynylisoxazoles (III) and Subsequent Sonogashira Coupling.

ChemInform ◽  
2016 ◽  
Vol 47 (6) ◽  
pp. no-no
Author(s):  
Shravankumar Kankala ◽  
Sreekantha B. Jonnalagadda ◽  
Chandra Sekhar Vasam
RSC Advances ◽  
2015 ◽  
Vol 5 (93) ◽  
pp. 76582-76587 ◽  
Author(s):  
Shravankumar Kankala ◽  
Sreekantha B. Jonnalagadda ◽  
Chandra Sekhar Vasam

An organo-NHC catalysed domino addition approach for the selective synthesis of 5-butynylisoxazoles and the subsequent Sonogashira cross-coupling for the selective synthesis of corresponding internal alkynes is described.


2015 ◽  
Vol 357 (14-15) ◽  
pp. 3052-3056 ◽  
Author(s):  
Shanfei Pan ◽  
Xueji Ma ◽  
Danni Zhong ◽  
Wanzhi Chen ◽  
Miaochang Liu ◽  
...  

ChemInform ◽  
2016 ◽  
Vol 47 (8) ◽  
pp. no-no
Author(s):  
Shanfei Pan ◽  
Xueji Ma ◽  
Danni Zhong ◽  
Wanzhi Chen ◽  
Miaochang Liu ◽  
...  

Author(s):  
William Finnigan ◽  
Lorna J. Hepworth ◽  
Nicholas J. Turner ◽  
Sabine Flitsch

As the enzyme toolbox for biocatalysis has expanded, so has the potential for the construction of powerful enzymatic cascades for efficient and selective synthesis of target molecules. Additionally, recent advances in computer-aided synthesis planning (CASP) are revolutionizing synthesis design in both synthetic biology and organic chemistry. However, the potential for biocatalysis is not well captured by tools currently available in either field. Here we present RetroBioCat, an intuitive and accessible tool for computer-aided design of biocatalytic cascades, freely available at retrobiocat.com. Our approach uses a set of expertly encoded reaction rules encompassing the enzyme toolbox for biocatalysis, and a system for identifying literature precedent for enzymes with the correct substrate specificity where this is available. Applying these rules for automated biocatalytic retrosynthesis, we show our tool to be capable of identifying promising biocatalytic pathways to target molecules, validated using a test-set of recent cascades described in the literature.


2018 ◽  
Author(s):  
Matthew L. Landry ◽  
Grace McKenna ◽  
Noah Burns

A concise and selective synthesis of the dichlorinated meroterpenoid azamerone is described. The paucity of tactics for the synthesis of chiral organochlorides motivated the development of unique strategies for accessing these motifs in enantioenriched forms. The route features a novel enantioselective chloroetherification reaction, a Pd-catalyzed cross-coupling between a quinone diazide and a boronic hemiester, and a late-stage tetrazine [4+2]-cycloaddition/oxidation cascade.


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