Kuang, C., Yang, Q., Senboku, H. and Tokuda, M. (2005) Synthesis of (Z)-1-bromo-1-alkenes and Terminal Alkynes from Anti-2,3-dibromoalkanoic Acids by Microwave Induced Reaction. Tetrahedron, 61, 4043-4052.
http://dx.doi.org/10.1016/j.tet.2005.02.043

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).