α-Phosphonovinyl nonaflate: Their synthesis and cross-coupling reactions

Tetrahedron Letters

Volumn 40, Issue 29, 1999, Pages 5337-5340

  Okauchi, Tatsuo ^a   Yano, Tomomi ^a   Fukamachi, Takeshi ^a   Ichikawa, Junji ^a   Minami, Toru ^a  

^a KYUSHU INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

Dienes; Enynes; Phosphonic acids and derivatives; Sulfonic acid and derivatives

Indexed keywords

ALKADIENE; PALLADIUM; PHOSPHONIC ACID DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; SYNTHESIS;

EID: 0033575422     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00971-5     Document Type: Article

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15. Acylphosphonates 1a-d were prepared from acid chloride and triethylphosphite following literature procedures: Berlin, K. D.; Hellwege, D. M.; Nagabhushanam, M. J. Org. Chem. 1965, 30, 1265; Takamizawa, A.; Sato, Y.; Sato, H. Chem. Pharm. Bull. 1967, 15, 1183; Tam, C. C; Mattocks, K. L.; Tishler, M. Proc. Natl. Acad. Sci. USA 1981, 78, 3301.
16. Acylphosphonates 1a-d were prepared from acid chloride and triethylphosphite following literature procedures: Berlin, K. D.; Hellwege, D. M.; Nagabhushanam, M. J. Org. Chem. 1965, 30, 1265; Takamizawa, A.; Sato, Y.; Sato, H. Chem. Pharm. Bull. 1967, 15, 1183; Tam, C. C; Mattocks, K. L.; Tishler, M. Proc. Natl. Acad. Sci. USA 1981, 78, 3301.
17. Nonafluorobutanesulfonyl fluoride is commercially available.
18. 6PS: C, 25.99; H, 2.62%.
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