Hypervalent iodine in synthesis. XXVII. Alkynylphenyliodonium tosylates as alkynylating reagents: Direct conversion of alkynylphenyliodonium tosylates to dialkyl alkynylphosphonates with sodium dialkylphosphonates

Synthetic Communications

Volumn 28, Issue 1, 1998, Pages 175-179

  Zhang, Jun Lian ^a   Chen, Zhen Chu ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNYL GROUP; ALKYNYLPHENYLIODINIUM TOSYLATE; DIALKYLALKYNYLPHOSPHONATE; IODINE; PHOSPHONIC ACID DERIVATIVE; REAGENT; SODIUM DIALKYLPHOSPHONATE; UNCLASSIFIED DRUG;

ARTICLE; SYNTHESIS;

EID: 0031889589     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919808005087     Document Type: Article

References (13)

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11. Hypervalent Iodine in synthesis XXV I Zhang, J. L.; Chen, Z. C.; Synth. Commun. to be submitted.
12. For recently review, see: Stang, P. J.; Zhdankin, V. V., Chem. Rev. 1996, 96, 1123
13. Lodaya and Koser reported that alkynylphenyliodonium tosylates react with trimethyl phosphite in formal Arbusov fashion to give alkynylphosphonates. Lodaya, J. S., Koser, G. F. J. Org. Chem. 1990, 55, 1513