Single-step construction of an acetoxypyrroloindole skeleton via tandem iodocyclization/acetoxylation of indoles

Org Biomol Chem. 2022 Jul 13;20(27):5397-5401. doi: 10.1039/d2ob01001a.

Abstract

A method for the synthesis of C3a acetoxy hexahydropyrrolo[2,3-b]indole derivatives via a PhI(OAc)2/nBu4NI mediated tandem iodocyclization/acetoxylation has been developed. The newly developed synthetic strategy features the single-step assembly of various C3a acetoxylated tetrahydropyrrole-, tetrahydrofuran-, and lactone-fused indolines under mild reaction conditions, which enabled efficient asymmetric synthesis of (-)-protubonine B.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Indoles*
  • Skeleton*

Substances

  • Indoles