-
Reagent for tert-Butoxycarbonylation: 2-tert-Butoxycarbonyloxyimino-2-
phenylacetonitrile".
Organic Syntheses. 6: 199. doi:10.15227/orgsyn.059.0095. Wawzonek...
- the
similar reaction with
phenacyl chloride, or the
reaction of
phenylacetonitrile with
methyl nitrite and
sodium hydroxide. An
isolated but classic...
- (R)-2-[(R)-1-Phenylpropan-2-ylamino]-2-
phenylacetonitrile (CAS
number 478392-08-4) (S)-2-[(S)-1-Phenylpropan-2-ylamino]-2-
phenylacetonitrile (CAS
number 478392-12-0)...
-
Bromobenzyl cyanide Names IUPAC name (RS)-2-bromo-2-
phenylacetonitrile Other names α-bromobenzyl
cyanide Identifiers CAS
Number 5798-79-8 Y 3D
model (JSmol)...
- \rightleftharpoons }
phenylacetonitrile + H2O Hence, this
enzyme has one substrate, (Z)-phenylacetaldehyde oxime, and two products,
phenylacetonitrile and H2O. This...
- CYP706C55
catalyzes the
dehydration of
phenylacetaldoxime to
phenylacetonitrile.
Phenylacetonitrile is then
hydroxylated by CYP71B103 to mandelonitrile. After...
- Taylor,
Harold M.; Hauser,
Charles R. (1973). "α-(N,N-Dimethylamino)
phenylacetonitrile".
Organic Syntheses;
Collected Volumes, vol. 5, p. 437. Soffer, M...
-
active methylene groups, such as
those of
malonic esters and
phenylacetonitrile.
Phenylacetonitrile (PhCH2CN)
gives the
imine (PhC(CN)=NPh) in a
reaction known...
-
Names IUPAC name (2R)-[β-D-Glucopyranosyl-(1→6)-β-D-glucopyranosyloxy]
phenylacetonitrile Systematic IUPAC name (2R)-Phenyl{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R...
- (Locusta migratoria) that
catalyzes the key step of
biosynthesis of
phenylacetonitrile (PAN). PAN in turn is used as an
aposematic chemical defense against...