Molecular complexity from aromatics: synthesis and photoreaction of endo-tricyclo[5.2.2.02,6]undecane—A stereoselective route to tricyclic framework of protoilludanes

SINGH, VISHWAKARMA
LAHIRI, SANJOY
PAL, SHANTANU

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Publication date

January 2005

DOI

10.1016/j.bmcl.2005.06.030

Publisher

Elsevier BV

Journal

Bioorganic & Medicinal Chemistry Letters

Abstract

A stereoselective route towards protoilludanoids from simple aromatic precursor is described. The methodology involves in situ generation of spiroepoxycyclohexadienone and cycloaddition with cyclopentadiene and photochemical 1,3-acyl shift.© Elsevie

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Molecular complexity from aromatics: synthesis and photoreaction of endo-tricyclo[5.2.2.02,6]undecane—A stereoselective route to tricyclic framework of protoilludanes

Abstract

Extracted data

Molecular complexity from aromatics: synthesis and photoreaction of endo-tricyclo[5.2.2.02,6]undecane—A stereoselective route to tricyclic framework of protoilludanes

Abstract

Extracted data

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