Synthesis of novel and diverse naphtho[1,2-b]furans by phosphine-catalyzed [3+2] annulation of activated 1,4-naphthoquinones and acetylenecarboxylates

Mol Divers. 2015 Feb;19(1):55-66. doi: 10.1007/s11030-014-9555-1. Epub 2014 Oct 1.

Abstract

A new phosphine-catalyzed [3+2] annulation reaction between activated 1,4-naphthoquinones and acetylenecarboxylates is described. This reaction provides a facile and efficient route to a variety of biologically promising and novel naphtho[1,2-b]furans. This devised method provides a first example for the synthesis of diverse naphtho[1,2-b]furan derivatives from 1,4-naphthoquinones via phosphine-catalyzed [3+2] annulation. A variety of novel naphtho[1,2-b]furans were synthesized via the phosphine-catalyzed [3+2] annulation of activated 1,4-naphthoquinones and electron-deficient acetylenecarboxylates. In some reactions, both furannulation adducts and reductive/nucleophilic conjugate addition products were produced.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylene / chemistry*
  • Carboxylic Acids / chemistry
  • Chemistry Techniques, Synthetic
  • Furans / chemical synthesis*
  • Furans / chemistry*
  • Naphthoquinones / chemistry*
  • Phosphines / chemistry*

Substances

  • Carboxylic Acids
  • Furans
  • Naphthoquinones
  • Phosphines
  • phosphine
  • Acetylene
  • 1,4-naphthoquinone