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T. Minami, K. Nishimura, I. Hirao, H. Suganuma and T. Agawa, “Reactions of Vinylphosphonates. 2. Synthesis of Functionalized Dienes, Trienes, and Their Analogues. Synthetic Applications to Regioselectively Functionalized Benzene Derivatives,” The Journal of Organic Chemistry, Vol. 47, No. 12, 1982, pp. 2360-2363.
doi:10.1021/jo00133a025
has been cited by the following article:
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TITLE:
Three-Component Coupling Catalyzed by Phosphine: Preparation of α-Amino γ-Oxo Acid Derivatives
AUTHORS:
Yohei Oe, Takeshi Inoue, Hiroaki Kishimoto, Mitsuhiro Sasaki, Tetsuo Ohta, Isao Furukawa
KEYWORDS:
Three-Component Coupling; Phosphine; 2-Amino-4-Oxocarboxylic Acid
JOURNAL NAME:
International Journal of Organic Chemistry,
Vol.2 No.2,
June
27,
2012
ABSTRACT: The three-component coupling reaction of ethyl propiolate (1), phthalimide (2), and aldehyde (3) catalyzed by tripheny- lphosphine, was developed. A solution of an equivalent amount of 1 and 2 in benzaldehyde (3a) in the presence of 30 mol% of PPh3 was heated at 100?C for 48 h to give N-(1-ethoxycarbonyl-3-oxo-3-phenylpropyl)phthalimide (4a) in 83% yield. This reaction was thought to proceed via vinylphosphonium salt formed from the reaction of ethyl propiolate (1) with triphenylphosphine in situ.