Trimethylsilyl halide-promoted Michaelis-Arbuzov rearrangement

Organic Letters

Volumn 5, Issue 10, 2003, Pages 1661-1664

  Renard, Pierre Yves ^a   Vayron, Philippe ^a   Mioskowski, Charles ^b  

^a CEA SACLAY   (France)

^b UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HALIDE; TRIMETHYLSILYL DERIVATIVE;

ADDITION REACTION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; MICHAELIS ARBUZOV REARRANGEMENT; REACTION ANALYSIS; ROOM TEMPERATURE; STRUCTURE ANALYSIS; SYNTHESIS; TECHNIQUE; TEMPERATURE DEPENDENCE;

EID: 0141852881     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0342913     Document Type: Article

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21. Contrary to results obtained with other phosphorus(III) esters, the best final yields were obtained when the cyclic phosphonite was prepared as described in Scheme 9 from the corresponding phosphoramidite 23, not from the chlorophosphonite.
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23. Both cyclic phosphinates conformed to the literature description: (a) Chaudhry, A.; Harger, M. J.; Shuff, P.; Thompson A. J. Chem. Soc., Perkin Trans. 1 1999, 1347-1352. (b) Singh, G.; Reddy, G. S.; Calabrese, J. C. J. Org. Chem. 1984, 49, 5132-5136.