915286-93-0

Upstream product

• 915286-75-8 7-[2'-deoxy-3',5'-di-O-mesyl-β-D-threo-pentofuranosyl]-2-isobutyrylamino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine 
• 21740-23-8 3,5-O-bis(4-chlorobenzoyl)-2-deoxy-α-D-ribofuranosyl chloride 
• 86392-74-7 2-amino-9-(2'-deoxy-β-D-erythro-pentofuranosyl)-6-methoxyl-7H-pyrrolo[2,3-d]pyrimidine 
• 915286-73-6 7-[2'-deoxy-3',5'-di-O-(4-nitrobenzoyl)-β-D-threo-pentofuranosyl]-2-isobutyrylamino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine 
• 915286-82-7 7-[2'-deoxy-3'-O-mesyl-5'-O-(4-monomethoxytrityl)-β-D-threo-pentofuranosyl]-2-isobutyrylamino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine 
• 915286-79-2 7-[3'-amino-5'-(4-monomethoxytritylamino)-2',3',5'-trideoxy-β-D-erythro-pentofuranosyl]-2-isobutyrylamino-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one 
• 915286-84-9 7-[3'-azido-2',3'-dideoxy-5'-O-(4-monomethoxytrityl)-β-D-erythro-pentofuranosyl]-2-isobutyrylamino-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one 
• 915286-83-8 7-[3'-azido-5'-O-(4-monomethoxytrityl)-2',3'-dideoxy-β-D-erythro-pentofuranosyl]-2-isobutyrylamino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine 
• 915286-85-0 7-[3'-amino-2',3'-dideoxy-5'-O-(4-monomethoxytrityl)-β-D-erythro-pentofuranosyl]-2-isobutyrylamino-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one 
• 915286-81-6 7-[2'-deoxy-5'-O-(4-monomethoxytrityl)-β-D-threo-pentofuranosyl]-2-isobutyrylamino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine 
• 915286-72-5 2-amino-4-chloro-7-[2'-deoxy-3',5'-di-O-(4-chlorobenzoyl)-β-D-erythro-pentofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine 
• 915286-77-0 7-[3',5'-diazido-2',3',5'-trideoxy-β-D-erythro-pentofuranosyl]-2-isobutyrylamino-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one 
• 915286-76-9 7-[3',5'-diazido-2',3',5'-trideoxy-β-D-erythro-pentofuranosyl]-2-isobutyrylamino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine 
• 915286-78-1 7-[3',5'-diamino-2',3',5'-trideoxy-β-D-erythro-pentofuranosyl]-2-isobutyrylamino-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one 

Relevant academic research and scientific papers

Solid-phase synthesis of positively charged deoxynucleic guanidine (DNG) oligonucleotide incorporating 7-deazaguanine bases

DNG nucleotides represent a positively charged DNA analog in which the negatively charged phosphodiester linkages of DNA are replaced by positively charged guanidinium linkages. We report herein the synthesis of 3′-end, middle, and 5′-end monomers require