1962
DOI: 10.1016/0031-6458(62)90054-0
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of esters by the carbalkoxylation of olefins with carbon monoxide

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

1978
1978
2019
2019

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(3 citation statements)
references
References 1 publication
0
3
0
Order By: Relevance
“…This could be caused either by an altered focal volume due to changes in the refractive index or a nonideal mixing behavior of MMB and methanol. The refractive indices of the neat liquids MMB (n D 20 = 1.393 44 ) and deuterated methanol (n D 20 = 1.326 according to the manufacturer) are close to each other. Further, for all measurements, an excess of MMB was used, and thus, the contribution of MMB should predominate the refractive index of the mixture.…”
Section: ■ Resultsmentioning
confidence: 78%
“…This could be caused either by an altered focal volume due to changes in the refractive index or a nonideal mixing behavior of MMB and methanol. The refractive indices of the neat liquids MMB (n D 20 = 1.393 44 ) and deuterated methanol (n D 20 = 1.326 according to the manufacturer) are close to each other. Further, for all measurements, an excess of MMB was used, and thus, the contribution of MMB should predominate the refractive index of the mixture.…”
Section: ■ Resultsmentioning
confidence: 78%
“…1-Methylcyclopentanecarboxaldehyde: The products were methylenecyclopentane,56 1-methylcyclopentene,57 1-chloro-l-methylcyclopentane,54 and ethyl 1-methylcyclopentanecarboxylate. 48 The first two products were shown to arise from the third in the injection port of the gas chromatograph. The analysis was done on column A, programmed between 50 and 233 °C.…”
Section: Methodsmentioning
confidence: 99%
“…Cyclopentanecarboxaldehyde: The products were chlorocyclopentane and ethyl cyclopentanecarboxylate. 48 The analysis was done on column B, programmed between 50 and 230 °C. A control showed that a mixture of chlorocyclopentane and cyclopentanecarbonyl chloride did not change composition when included in a decarbonylation run of cyclobutanecarboxaldehyde.…”
Section: Methodsmentioning
confidence: 99%