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Mol Divers ; 24(3): 707-716, 2020 Aug.
Article in English | MEDLINE | ID: mdl-31363886

ABSTRACT

A simple method for the synthesis of functionalized 2H-pyrans via a catalytic reaction of an oxirane, an alkyne, and a malonate has been developed in which a 6-exo-dig cyclization pathway is observed. In this transformation, the attack of in situ generated copper acetylides on oxiranes formed homopropargylic alcohol intermediates which further transferred to 2H-pyrans with the help of malonates.


Subject(s)
Carboxylic Acids/chemistry , Carboxylic Acids/chemical synthesis , Pyrans/chemistry , Chemistry Techniques, Synthetic , Cyclization , Ethylene Oxide/chemistry , Malonates/chemistry
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