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- W2950341773 abstract "Treatment of propargylic dithiolanes 1 with nBuLi followed by a carbonyl electrophile yields the corresponding homopropargylic alcohol 3. Upon treatment with 2 equiv of PPh3 and DIAD, elimination of SR and OH moieties from 3 affords the corresponding olefins 4 in moderate to good yield. The reaction can be considered an alternative of McMurry coupling of two different carbonyl equivalents." @default.
- W2950341773 created "2019-06-27" @default.
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- W2950341773 date "2009-03-24" @default.
- W2950341773 modified "2023-09-24" @default.
- W2950341773 title "ChemInform Abstract: Elimination of β-Thioalkoxy Alcohols under Mitsunobu Conditions. A New Synthesis of Conjugated Enynes from Propargylic Dithioacetals." @default.
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- W2950341773 doi "https://doi.org/10.1002/chin.200912049" @default.
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