{ALD} Beilstein: 16,IV,980

{PUB} ChemIDplus --- U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals., NX#12281 ---

{ALFA} For reaction with trifluoroacetic anhydride and triethylamine, followed by pyrolysis as a route to perfluoroalkyl acetylenes, see: Org. Synth. Coll., 9, 436 (1998):

{PUB} Thieme Chemistry --- Alkylation of Phosphines with α-(Halomethyl)carbonyl Species --- https://science-of-synthesis.thieme.com/app/text/?id=SD-042-00577

{PUB} Thieme Chemistry --- Condensation of Esters with Organophosphorus Reagents (Wittig-like Reaction) --- https://science-of-synthesis.thieme.com/app/text/?id=SD-032-00674

{PUB} Thieme Chemistry --- Cyclization of γ-Oxo Acids --- https://science-of-synthesis.thieme.com/app/text/?id=SD-109-00807

{PUB} Thieme Chemistry --- Modification of Ketones, Aldehydes, and Derivatives --- https://science-of-synthesis.thieme.com/app/text/?id=SD-016-00449

{PUB} Thieme Chemistry --- Reaction of Stabilized Ylides with Other Electrophiles --- https://science-of-synthesis.thieme.com/app/text/?id=SD-042-00579

{PUB} Thieme Chemistry --- Reaction of[(Alkoxycarbonyl)methylene]triphenylphosphoranes with Acyl Chlorides, Anhydrides, or Carboxylic Acids --- https://science-of-synthesis.thieme.com/app/text/?id=SD-020-01193

{PUB} Thieme Chemistry --- Reaction of[(Ethoxycarbonyl)iodomethyl]triphenylphosphonium Iodide with Aldehydes --- https://science-of-synthesis.thieme.com/app/text/?id=SD-020-01194