Carbopeptoids and carbonucleotoids

A step-wise process for synthesizing an oligomeric carbopeptoid compound comprising the following steps:

• Step A:
• coupling two carbohydrate amino acid subunits (CA's) to one another by means of an amide linkage having a carbonyl carbon and an amido nitrogen for synthesizing a carbopeptoid dimer represented by a formula as follows:
• CA1-(CO—NH)-CA2
• wherein:
• CA1 is a first carbohydrate amino acid subunit having a non-anomeric carbon bonded to a differentially protected amino group and an anomeric carbon bonded to the carbonyl carbon of said amide linkage for forming a C-glycosyl linkage therewith;
• and
• CA2 is a second carbohydrate amino acid subunit having an anomeric carbon bonded to a protected carboxyl group and a non-anomeric carbon bonded to the amido nitrogen of said amide linkage;
• then
• Step B:
• deprotecting the differentially protected amino group on the non-anomeric carbon of CA1 of said Step A for producing a differentially deprotected carbopeptoid dimer;
• and then
• Step C:
• elongating the deprotected carbopeptoid dimer of said step B by a step-wise addition of one or more additional carbohydrate amino acid subunits via amide linkages for producing said oligomeric carbopeptoid compound.

A process for synthesizing a library of oligomeric carbopeptoids incorporating “n” carbohydrate amino acid subunits, “n” being three or greater, the process comprising the following steps:

• Step A:
• performing a first split synthesis for producing a library of carbopeptoid dimers incorporating the “n” carbohydrate amino acid subunits, each carbopeptoid dimer including two of the “n” carbohydrate amino acid subunits (CA's) coupled to one another via an amide linkage having a carbonyl carbon and an amido nitrogen represented by the following formula:
• CA1-(CO—NH)-CA2
• wherein:
• CA1 is a carbohydrate amino acid subunit in a first position of said carbopeptoid dimer having a non-anomeric carbon with a differentially protected amino group and an anomeric carbon bonded to the carbonyl carbon of a first amide linkage;
• and
• CA2 is a carbohydrate amino acid subunit in a second position of said carbopeptoid dimer having a non-anomeric carbon bonded to the amido nitrogen of said amide linkage;
• then
• Step B:
• deprotecting the differentially protected amino group on the non-anomeric carbon of the carbohydrate amino acid subunit of the first position of the library of carbopeptoid dimers in said Step A for producing a library of deprotected carbopeptoid dimers;
• then
• Step C:
• performing a second split synthesis for elongating the library of deprotected carbopeptoid dimers of said step B and producing a library of carbopeptoid trimers incorporating the “n” carbohydrate amino acid subunits, each carbopeptoid trimer including three of the “n” carbohydrate amino acid subunits (CA's) coupled to one another via amide linkages;
• and then optionally
• Step D:
• performing one or more additional second split syntheses for further elongating the carbopeptoid trimer of said step C and producing a library of oligomeric carbopeptoids incorporating the “n” carbohydrate amino acid subunits, each oligomeric carbopeptoids including more than three of the “n” carbohydrate amino acid subunits (CA's) coupled to one another via amide linkages.

An oligomeric carbonucleotoid molecule comprising three or more carbohydrate C-glycosyl subunits (CG's) coupled to one another via phosphodiester linkages, said oligomeric carbonucleotoid being represented by the following structure:

• CG1-C1′—(O—PO(OH)—O)-CG2-C2′—(O—PO(OH)—O)-CG3 . . .
• wherein:
• CG1-C1′ is a first carbohydrate C-glycosyl subunit having an anomeric carbon forming a C-glycosyl bond with a carbon C1′, said carbon C1′ being bonded to a first phosphodiester linkage for linking to CG2-C2′;
• CG2-C2′ is a second carbohydrate C-glycosyl subunit having a non-anomeric carbon bonded to said first phosphodiester linkage for linking to CG1-C1′ and an anomeric carbon forming a C-glycosyl bond with a carbon C2′, said carbon C2′ being bonded to a second phosphodiester linkage for linking to CG3;
• and
• CG3 is a third carbohydrate C-glycosyl subunit having a non-anomeric carbon bonded to said second phosphodiester linkage for linking to CG2-C2′.

A step-wise process for synthesizing an oligomeric carbonucleotoid molecule comprising the following steps:

• Step A:
• coupling two carbohydrate C-glycosyl subunits (CG's) to one another by means of a phosphodiester linkage for synthesizing a carbonucleotoid dimer represented by a formula as follows:
• CG1-C1′—(O—PO(OH)—O)-CG2
• wherein:
• CG1-C1′ is a first carbohydrate C-glycosyl subunit having a non-anomeric carbon with a differentially protected hydroxyl group and having an anomeric carbon forming a C-glycosyl bond with a carbon C1′, said carbon C1′ being bonded to said phosphodiester linkage;
• and
• CG2 is a second carbohydrate C-glycosyl subunit having a non-anomeric carbon bonded to said phosphodiester linkages;
• then
• Step B:
• deprotecting the differentially protected hydroxyl group of the first carbohydrate C-glycosyl subunit CG1-C1′ of said Step A for producing a differentially deprotected carbonucleotoid dimer;
• and then
• Step C:
• elongating the deprotected carbonucleotoid dimer of said step B by a step-wise addition of one or more additional carbohydrate C-glycosyl subunits via phosphodiester linkages for producing said oligomeric carbonucleotoid compound.

A process for synthesizing a library of oligomeric carbonucleotoids incorporating “n” carbohydrate C-glycosyl subunits, “N” being three or greater, the process comprising the following steps:

• Step A:
• performing a first split synthesis for producing a library of carbonucleotoid dimers incorporating the “n” carbohydrate C-glycosyl subunits, each carbonucleotoid dimer including two of the “n” carbohydrate C-glycosyl subunits (CG's) coupled to one another by means of a phosphodiester linkage, said phosphodiester linkage being represented by a formula as follows:
• CG1-C′—(O—PO(OH)—O)-CG2
• wherein:
• CG1-C1′ is a carbohydrate C-glycosyl subunit in a first position of said carbonucleotoid dimer having a non-anomeric carbon with a differentially protected hydroxyl group and an anomeric carbon forming a C-glycosyl bond with a carbon C1′, said carbon C1′ being bonded to a first phosphodiester linkage;
• and
• CG2 is a carbohydrate C-glycosyl subunit in a second position of said carbonucleotoid dimer having a non-anomeric carbon bonded to said first phosphodiester linkage;
• then
• Step B:
• deprotecting the differentially protected hydroxyl group on the non-anomeric carbon of the carbohydrate C-glycosyl subunit of the first position of the library of carbonucleotoid dimers in said Step A for producing a library of deprotected carbonucleotoid dimers;
• then
• Step C:
• performing a second split synthesis for elongating the library of deprotected carbonucleotoid dimers of said step B and producing a library of carbonucleotoid trimers incorporating the “n” carbohydrate C-glycosyl subunits, each carbonucleotoid trimer including three of the “n” carbohydrate C-glycosyl (CG's) coupled to one another via phosphodiester linkages;
• and then optionally
• Step D:
• performing one or more additional second split syntheses for further elongating the carbonucleotoid trimer of said step C and producing a library of oligomeric carbonucleotoids incorporating the “n” carbohydrate C-glycosyl subunits, each oligomeric carbonucleotoids including more than three of the “n” carbohydrate C-glycosyl subunits (CG's) coupled to one another via phosphodiester linkages.