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3- Phenyl-2-methyl-2-propenal,

A cationic Ir complex possessing phosphanodihydrooxazole 26 is usable for asymmetric hydrogenation of allylic alcohols. (E)-2-Methyl-3-phenyl-2-propen-l-ol can be converted in CH2C12 containing 1 mol % of the Ir complex to the saturated product in 95% yield and 96% ee (Scheme 1.26) [141]. The process is used in the enantioselective synthesis of the artificial fragrance filial. [Pg.29]

Benzyl-2-propen- IX, 504 2-Methyl-3-phenyl-2-propen- IX, 504 Thiokohlensaure -S-benzylester-O-... [Pg.758]

SYNS FEMA No. 2697 METHYL CINNAMIC ALDEHYDE a-METHYLCINNAMIC ALDEHYDE O-METHYLCINNIMAL 2-METHYL-3-PHENYL-2-PROPENAL... [Pg.913]

METHYL-3-PHENYL-2-PROPENAL see MIOOOO xMETHYL-3-PHENYLPROPENOATE see MI0500... [Pg.1780]

C10H10O 2-methyl-3-phenyl-2-propenal 101-39-3 521.15 45.920 1,2 19181 Cl OH1003 methyl benzoylacetate 614-27-7 538.15 47.561 2... [Pg.491]

C10H12O trans-2-methyl-3-phenyl-2-propen-1-ol 1504-55-8 502.76 44.150 2 19610 C10H12O2 4-propyl benzoic acid 2438-05-3 504.61 44.327 2... [Pg.493]

Propanoic acid, 2-methyl-, 3-phenyl-2-propen-l-yl ester... [Pg.385]

Methyl-1-phenyl-1-propanone 2-Methyl-3-phenyl-2-propenal... [Pg.493]

Synonyms Methyl cinnamic aldehyde o-Methyl cinnamic aldehyde o-Methyl cinnimal 2-Methyl-3-phenyl-2-propenal 2-Methyl-3-phenyl-propenyl... [Pg.2605]

Methyl-3-phenyl-2-propen-1 -ol o-Methyl-3-phenyl-2-propen-1-ol trans-2-Methyl-3-phenyl-2-propen-1-ol 3-Phenyl-2-methyl-propen-2-ol-1 2-Propen-1-ol, 2-methyl-3-phenyl-... [Pg.2606]

Methyl-2-phenylpropane. See t-Butylbenzene 2-(4-Methylphenyl)-2-propanol. See Tri methyl benzyl alcohol 2-Methyl-3-phenyl-2-propenal. See a-Methylcinnamaldehyde 2-(p-Methylphenyl) propene. See p-a-Di methylstyrene... [Pg.2676]

Mechanisms for decarbonylation of ( )-2-butenal and ( )-2-methyl-3-phenyl-2-propenal have been studied with different levels of ab initio and DFT methods. Reactants, products, and transition structures were optimized for two kinds of reaction channels a one-step reaction involving a three-membered cyclic TS, and a two-step reaction involving an initial four-membered cyclic TS. The elimination of ( )-2-methyl-3-phenyl-2-propenal yields different products depending on the channel followed. Only one of the three possible one-step mechanisms leads directly to (E)-P-methylstyrene, the corresponding TS rising to the lowest activation Gibbs free energy. [Pg.364]

See other pages where 3- Phenyl-2-methyl-2-propenal, is mentioned: [Pg.21]    [Pg.492]    [Pg.484]    [Pg.304]    [Pg.884]    [Pg.471]    [Pg.472]    [Pg.533]    [Pg.534]    [Pg.528]    [Pg.521]    [Pg.532]    [Pg.484]    [Pg.485]   
See also in sourсe #XX -- [ Pg.201 ]

See also in sourсe #XX -- [ Pg.201 ]



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2-Methyl-2-propen

3-Phenyl-2-propen

3-Phenyl-2-propenal

4- -phenyl]-2-methyl-propen

4- -phenyl]-2-methyl-propen

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