Isomerism and Polymorphism of Cinnam' ic Acids. VII. Preparation of cis-Cinnamic Acid by the Partial Catalytic Hydrogenation of Phenylpropiolic Acid

Urushibara, Yoshiyuki; Hirota, Minoru

doi:10.1246/nikkashi1948.85.10_679

Search citation statements

Order By: Relevance

Paper Sections

Select...

Z-selective Catalytic Hydrogenation Of Alkynes1

Citation Types

Supporting

Mentioning

Contrasting

Publication Types

Select...

Other1

Relationship

Self Cite0

Independent1

Authors

Journals

Cited by 2 publications

(2 citation statements)

References 0 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The yield was quite good, more than 90% and the Z:E selectivity was around 95:5. 57 An interesting variant of the Lindlar procedure is the so-called P-2 nickel catalyst, which is a Ni2B powder, (usually generated in situ), which shows high Z selectivity for alkyne hydrogenation. 58…”

Section: Z-selective Catalytic Hydrogenation Of Alkynesmentioning

confidence: 99%

See 1 more Smart Citation

Stereoselective synthesis and self-assembling capabilities of heterocyclic cinnamic acids

Csankó¹

View full text Add to dashboard Cite

E32F − E-3-(2-furyl)propenoic acid E32T − E-3-(2-thienyl)propenoic acid E32S − E-3-(2-selenienyl)propenoic acid E33P − E-3-(3-pyridyl)propenoic acid E23T33T-E-2-(3-thienyl)-3-(3-thienyl)propenoic acid Z2Ph33P-Z-2-phenyl-3-(3-pyridyl)propenoic acid Z − "Z" instead of "E" before the shorthand names of the materials listed above, means the Z isomer M − at the end of the shorthand names of the materials listed above, means the individual monomer

show abstract

Section: Z-selective Catalytic Hydrogenation Of Alkynesmentioning

confidence: 99%

“…The esterification of E32T and E33T with n-octanol(57) 1 eq. of E32T or E33T was dissolved in 55 and the solution was cooled to 0°C.…”

mentioning

confidence: 99%

Stereoselective synthesis and self-assembling capabilities of heterocyclic cinnamic acids

Csankó¹

View full text Add to dashboard Cite

show abstract

Isomerism and Polymorphism of Cinnam' ic Acids. VII. Preparation of cis-Cinnamic Acid by the Partial Catalytic Hydrogenation of Phenylpropiolic Acid

Cited by 2 publications

References 0 publications

Stereoselective synthesis and self-assembling capabilities of heterocyclic cinnamic acids

Stereoselective synthesis and self-assembling capabilities of heterocyclic cinnamic acids

Contact Info

Product

Resources

About