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• W2082783011 endingPage "3490" @default.
• W2082783011 startingPage "3481" @default.
• W2082783011 abstract "Highly site- and regioselective terminal functionalizations of acyclic monoterpenes 1 via benzenesulfenyl chloride addition followed by hydrolysis assisted by silica gel, dehydrochlorination under neutral or weakly basic condition, or dehydrochlorination by strongly basic treatment respectively providing β-hydroxy sulfides 3, terminal methallylic sulfides 4, or vinylsulfides 5 are developed. Conversion of 4 to terminal trans-allylic alcohols 10 via sulfoxides 9 by the Evans procedure is also described." @default.
• W2082783011 created "2016-06-24" @default.
• W2082783011 creator A5026835119 @default.
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• W2082783011 date "1984-01-01" @default.
• W2082783011 modified "2023-10-17" @default.
• W2082783011 title "Facile functionalization of the isopropylidene terminus of acyclic monoterpenes by way of benzenesulfenyl chloride addition" @default.
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• W2082783011 doi "https://doi.org/10.1016/s0040-4020(01)91499-1" @default.
• W2082783011 hasPublicationYear "1984" @default.
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