2017Prayogik RasayanRequires access

Synthetic studies of antascomicin A: Construction of C1-C16 fragment

Jithender Reddy Vakiti, Subhash Ghosh

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Abstract

This communication describes the stereoselective synthesis of C1-C16 fragment of antascomicin A, a non-immunosuppressive immunophil-binding natural product. Evans aldol reaction was used extensively to install all the stereo centres present in the fragment. The hemikatel present in the fragment was synthesized via DMP-mediated oxidation of β-hydroxy amide followed by acid catalyzed hemiketalization.

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What this paper is about

This communication describes the stereoselective synthesis of C1-C16 fragment of antascomicin A, a non-immunosuppressive immunophil-binding natural product. Evans aldol reaction was used extensively to install all the stereo centres present in the fragment. The hemikatel present in the fragment was synthesized via DMP-mediated oxidation of β-hydroxy amide followed by acid catalyzed hemiketalization.

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Available abstract

This communication describes the stereoselective synthesis of C1-C16 fragment of antascomicin A, a non-immunosuppressive immunophil-binding natural product. Evans aldol reaction was used extensively to install all the stereo centres present in the fragment. The hemikatel present in the fragment was synthesized via DMP-mediated oxidation of β-hydroxy amide followed by acid catalyzed hemiketalization.

Key concepts: Fragment (logic), Aldol reaction, Stereoselectivity, Amide, Natural product, Stereochemistry, Chemistry, Combinatorial chemistry

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