1956
DOI: 10.1021/jo01115a018
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Pentaerythritol Derivatives. II. 3-Halomethyl-3-hydroxymethyl Oxetanes1

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1959
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Cited by 10 publications
(3 citation statements)
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“…Owing to the limitation of the raw material source, the chlorinated alcohol method is not used widely, but the process can reduce the production cost and environmental pollution. Some researchers have conducted research on the use of LBC 8–13. Zheng et al.…”
Section: Introductionmentioning
confidence: 99%
“…Owing to the limitation of the raw material source, the chlorinated alcohol method is not used widely, but the process can reduce the production cost and environmental pollution. Some researchers have conducted research on the use of LBC 8–13. Zheng et al.…”
Section: Introductionmentioning
confidence: 99%
“…Tribromide 1 was prepared in 68% yield from the reaction of pentaerythritol with 40% aqueous HBr solution in acetic acid [10]. Using a modified literature procedure, the ring closure reaction to form dibromide 2 successfully proceeded in the presence of sodium ethoxide, affording 2 in 62% yield [11]. Treatment of 2 with >2.0 equiv.…”
Section: Introductionmentioning
confidence: 99%
“…D. R. LeveringReceived July9, 1959 The synthesis of esters from olefins, carbon monoxide, and alcohols using metal carbonyls,…”
mentioning
confidence: 99%