Loading ...
an electrochemical quasi - passivation layerprimarily composedof phenyl groups
the fused systemsresultingfrom thecondensation with a phenyl group
the carbon atomscomposingthe phenyl groups
a complex aromatic compoundcomposedof phenyl groups
the solvent aromaticity , investiga(passive) is influenced byphenyl groups
a substituted or unsubstituted monovalent hydrocarbon group ( except for an alkenyl group ) is , 20mol% or more of R 5is composedof a phenyl group
an organic compoundcomposedof a phenyl group and a hydroxyl group
The hydride atom in these iridium complexesoriginatesfrom the same phenyl group
major admixture componentsInfluencephenyl
box player Andrew McNamara(passive) led bya Tulla group
in an asymmet - rically substituted isomer pairresultingin an asymmet - rically substituted isomer pair
in an asymmetrically substituted isomer pairresultingin an asymmetrically substituted isomer pair
in a block with a higher modulusresultingin a block with a higher modulus
the crystallization of the compounds ( H. Tokilin , H. Higashi , C. Hosokawa , EP 388 , 768 ( 1990preventsthe crystallization of the compounds ( H. Tokilin , H. Higashi , C. Hosokawa , EP 388 , 768 ( 1990
to increase processing speed and provide mental endurancedesignedto increase processing speed and provide mental endurance
the lipophilic biphenyl - containing EXP-7711createdthe lipophilic biphenyl - containing EXP-7711
activity orientationcreatesactivity orientation
from the acetophenoneoriginatingfrom the acetophenone
from substitution of a hydrogen atom at position 2 , 3 , or 4 of the phenyl group with a trialkylstannyl groupresultingfrom substitution of a hydrogen atom at position 2 , 3 , or 4 of the phenyl group with a trialkylstannyl group
from substitution of one hydrogen atom of the phenyl group with a trialkylstannyl groupresultingfrom substitution of one hydrogen atom of the phenyl group with a trialkylstannyl group
from substitution of one hydrogen atom of the phenyl group with a trialkylsilyl groupresultingfrom substitution of one hydrogen atom of the phenyl group with a trialkylsilyl group
to greater attractive energy than chloro groupleadsto greater attractive energy than chloro group
the disulfide bond(passive) influenced bythe disulfide bond
greater steric hindrance(passive) caused bygreater steric hindrance
in L - benzylhydantoinresultingin L - benzylhydantoin
in the emergence of new NOEsresultingin the emergence of new NOEs
in the indane structureresultingin the indane structure
to the β - lactone productled directlyto the β - lactone product
similar molecular interactions with respect to the first compound and the second compoundcausessimilar molecular interactions with respect to the first compound and the second compound
a molecular interaction similar to the first and second compoundscausesa molecular interaction similar to the first and second compounds