Examples of 'aminocarbonyl' in a sentence
Meaning of "aminocarbonyl"
Aminocarbonyl is a noun that refers to a chemical group containing an amine and a carbonyl functional group
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- The univalent radical NHâ‚‚CO- that is equivalent to the carboxamide functional group.
How to use "aminocarbonyl" in a sentence
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aminocarbonyl
Additional values include methoxy and aminocarbonyl.
Aminocarbonyl represents a free amide group.
Representative amide carboxy protecting groups are aminocarbonyl and loweralkylaminocarbonyl groups.
Preferably no aminocarbonyl functional compounds are added to the reaction mixture.
It will be appreciated that these may also be considered to be substituted aminocarbonyl groups.
A suitable aminocarbonyl group is acetamido.
Another aspect of the invention includes those compounds wherein Y is an optionally substituted aminocarbonyl.
Representative substituted aminocarbonyl groups include, those shown below.
In some embodiments, each RI is independently selected aminocarbonyl.
The term " aminocarbonylalkyl " denotes an aminocarbonyl group attached to an alkyl radical.
Representative amide carboxy protecting groups comprise, without limitation, aminocarbonyl and loweralkylaminocarbonyl groups.
The term " aminocarbonylalkyl " denotes an aminocarbonyl group which is attached to an alkyl radical.
A selected example of a specific substituent on Ra ' is aminocarbonyl.
Representative substituted aminocarbonyl groups include, for example, those shown below.
Particular examples of specific substituents on Ra include hydroxy, aminocarbonyl and methylaminocarbonyl.
See also
The term " aminocarbonylalkyl " embraces alkyl radicals substituted with aminocarbonyl radicals.
In another embodiment, the PSMA ligand is a aminocarbonyl derivative of pentanedioic acid.
The term " aminocarbonylalkyl " includes alkyl radicals substituted with aminocarbonyl radicals.
A substituted pyridinesulfonamide compound of this invention has a pyridine ring with an N-substituted aminocarbonyl group.
A is an w-amino aminocarbonyl cyclization spacer that forms a cyclic ureum derivative upon cyclization ;.
In certain embodiments of formula I, Rc is hydrogen and Rd is aminocarbonyl.
The term " aminocarbonylhaloalkyl " embraces aminocarbonyl radicals as defined above substituted on a haloalkyl radical.
Compound of Claim 21 wherein R represents an aminocarbonyl or an alkylaminocarbonyl radical.
The term " hydroxyaminocarbonyl " denotes an aminocarbonyl group which has been substituted with a hydroxy radical.
In certain embodiments of formula I, Rg is aminocarbonyl.
An X ' aminocarbonyl group may be obtained by treatment of an X ' chlorocarbonyl group with ammonia.
For reference compounds for formula I, Rc is hydrogen and Rd is aminocarbonyl.
An aminocarbonyl group of formula,.
Is lower alkoxy substituted by carboxy, lower alkoxycarbonyl, aminocarbonyl or mono - or di-lower alkylaminocarbonyl ;.
Representative examples of aminocarbonyl include, but are not limited, aminocarbonyl, dimethylaminocarbonyl, benzylaminocarbonyl, and ethylaminocarbonyl.
Figure 22 shows the synthesis of the acid protected paclitaxel-w-amino aminocarbonyl cyclisation spacer conjugate.
Representative examples of aminocarbonyl include, but are not limited, aminocarbonyl, dimethylaminocarbonyl, methylaminocarbonyl, and ethylaminocarbonyl.
The compound of any one of claims 1 to 3, wherein Y is an optionally substituted aminocarbonyl.
Represents aminocarbonyl or a NR3R4 group wherein.
A compound according to any one of claims 1 to 4 wherein R6 is halo, cyano or aminocarbonyl.
In some embodiments, R6 is aminocarbonyl or dimethylaminocarbonyl.
In some embodiments, each R1 is independently selected aminocarbonyl.
Is hydrogen, aminocarbonyl or carboxy ;.
In a special embodiment, R2 represents aminocarbonyl.
Is suitably hydrogen, cyano, aminocarbonyl or methyl, preferably R4 is hydrogen or cyano ;.
Most preferably R ' 2 is hydrogen or aminocarbonyl.
Stands for hydrogen atom or for cyano group, aminocarbonyl group, C1-4 alkoxycarbonyl group, carboxy group ;.
Especially preferred substituents include hydroxy, -SO2-CH3 and aminocarbonyl.
In an additional preferred embodiment, R5 is cyano or aminocarbonyl and R6 is imidazolyl.
A substituent standing for X ist, for example, acetyl, propanoyl, benzoyl, phthaloyl or aminocarbonyl.
Pyrrole 2,3-dicarboxylates can also be prepared from aminocarbonyl compounds CXXV.
Typical values of R18 include hydrogen, fluoro, chloro, cyano, methyl, trifluoromethyl and aminocarbonyl.
Selected examples of suitable substituents on Ra include hydroxy, aminocarbonyl and ( C1-6 ) alkylaminocarbonyl.
Another special group of compounds are those compounds of formula ( I ' ) wherein R4 ' is aminocarbonyl.
In one embodiment, R5 is aminocarbonyl.
