Feldman, K.S. (2006) Modern Pummerer-Type Reactions. Tetrahedron, 62, 5003-5034.
http://dx.doi.org/10.1016/j.tet.2006.03.004
Padwa, A. (2004) Tandem Methodology for Heterocyclic Synthesis. Pure and Applied Chemistry, 76, 1933-1952.
Bur, S.K. and Padwa, A. (2004) The Pummerer Reaction:? Methodology and Strategy for the Synthesis of Heterocyclic Compounds. Chemical Reviews, 104, 2401-2432.

has been cited by the following article:

• TITLE: Synthetic Studies of Naphtho[2,3-b]furan Moiety Present in Diverse Bioactive Natural Products

  AUTHORS: Bidyut Kumar Senapati, Dipakranjan Mal

  KEYWORDS: 6H-Furo[3, 4-b]furanone, Naphtho[2, 3-b]furan, Intramolecular Pummerer Reaction, Desulfanylation, Lactonization

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.5 No.2, May 29, 2015

  ABSTRACT: The preparation of several functionalized furan derivatives and attempts to transform them into a derivative containing 6H-furo[3,4-b]furanone skeleton towards the construction of naphtho[2,3-b] furan are described. Attempted Pummerer reaction of a furan sulfoxide derivative produced four interesting furan derivatives. Base promoted annulation between methyl 2-(phenylsulfinylmethyl)-3-furoate and 2-cyclohexenone proceeded to give dihydro naphtho[2,3-b]furanone derivative in a regiospecific manner.