2000
DOI: 10.1002/(sici)1099-0690(200001)2000:1<99::aid-ejoc99>3.0.co;2-1
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Mechanism and Extensibility of the Reaction

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Cited by 16 publications
(1 citation statement)
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“…For this reason, this type of reaction has not yet found general synthetic applications, especially for the extreme reaction conditions required . Even though organocerium reagents are reactive toward acidic hydrogen, some reaction conditions have been reported allowing an efficient cross-coupling between various RLi/CeCl 3 complexes and a range of allyl, homoallyl, and propargyl alcohols . The combination of both organollithium compounds and lithium hydride with dry CeCl 3 works very well (Scheme ), and products are obtained in moderate to good yields and without chromatographic purification of the crude product.…”
Section: Organocerium Compounds In Organic Chemistrymentioning
confidence: 99%
“…For this reason, this type of reaction has not yet found general synthetic applications, especially for the extreme reaction conditions required . Even though organocerium reagents are reactive toward acidic hydrogen, some reaction conditions have been reported allowing an efficient cross-coupling between various RLi/CeCl 3 complexes and a range of allyl, homoallyl, and propargyl alcohols . The combination of both organollithium compounds and lithium hydride with dry CeCl 3 works very well (Scheme ), and products are obtained in moderate to good yields and without chromatographic purification of the crude product.…”
Section: Organocerium Compounds In Organic Chemistrymentioning
confidence: 99%