Journal
ORGANIC LETTERS
Volume 2, Issue 24, Pages 3873-3875Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol0066173
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A method for the palladium-catalyzed synthesis of alkynylphosphonates from 1,l-dibromo-l-alkenes has been developed. In general, the best catalyst system for this transformation was found to be Pd(OAc)(2), dppf, H-phosphonate, propylene oxide, DMF, 80 degreesC, The reaction appears tolerant of a range of functional groups in both the 1,l-dibromo-l-alkene and H-phosphonate coupling partners. The synthesis of a backbone-modified thymidine dimer is used to illustrate the application of this methodology in the synthesis of complex target molecules.
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