Abarbri, M., Thibonnet, J., Parrain, J.-L. and Duchêne, A. (2002) Palladium-Catalyzed Cross-Coupling of Iodovinylic Acids with Organometallic Reagents. Selective Synthesis of 3,3-Disubstituted Prop-2-enoic Acids. Synthesis, 2002, 543-551.
http://dx.doi.org/10.1055/s-2002-20971

has been cited by the following article:

• TITLE: Facile, Direct Reaction of Benzaldehydes to 3-Arylprop-2-Enoic Acids and 3-Arylprop-2-Ynoic Acids in Aqueous Medium

  AUTHORS: Thies Thiemann, Mohamed W. Elshorbagy, Mostafa H. F. A. Salem, Siraj A. N. Ahmadani, Yosef Al-Jasem, Mariam Al Azani, Mazen A. M. Al-Sulaibi, Bassam Al-Hindawi

  KEYWORDS: Carboxylic Acids, Arylpropiolic Acids, Wittig Olefination, One Pot Reaction, Aqueous Reaction Medium, Dehydrobromination, Hydrolysis

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.2, June 3, 2016

  ABSTRACT: Wittig reactions of benzaldehydes, alkanals, and cycloalkanals as well as of acetophenones are carried out with alkoxycarbonyl methylidenetriphenylphosphoranes in 10 w% aqueous NaOH, where the cinnamates and alkenoates produced are hydrolysed in situ and the corresponding acids are obtained after mostly simple extractive work-up, often without employing organic solvents. Under the same conditions, benzaldehydes are reacted with alkoxycarbonyl bromomethy-lidenephosphorane to produce 3-arylprop-2-ynoic acids (arylpropiolic acids).