2014
DOI: 10.1016/j.tetlet.2014.08.012
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Modification of guanosine with cyanopropargylic alcohols

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Cited by 3 publications
(1 citation statement)
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“…The second was 1:2 adducts 132 with another molecule of cyanoacetylene 1 attached to the ribose fragment through its two vicinal hydroxy groups, forming 1,3-dioxolanes in 29-50% yields (Scheme 86). 172,178 Both modifications 131 and 132 can be cleanly separated, thereby enabling two different derivatives of low reactive 173c guanosine to be obtained via a single preparative procedure.…”
Section: Guanosinementioning
confidence: 99%
“…The second was 1:2 adducts 132 with another molecule of cyanoacetylene 1 attached to the ribose fragment through its two vicinal hydroxy groups, forming 1,3-dioxolanes in 29-50% yields (Scheme 86). 172,178 Both modifications 131 and 132 can be cleanly separated, thereby enabling two different derivatives of low reactive 173c guanosine to be obtained via a single preparative procedure.…”
Section: Guanosinementioning
confidence: 99%