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1-[2'-DEOXY-3',5'-BIS-O-(4-METHYLBENZOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-4-NITRO-1H-INDAZOLE

Compound with spectra: 1 NMR

1-[2'-DEOXY-3',5'-BIS-O-(4-METHYLBENZOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-4-NITRO-1H-INDAZOLE
SpectraBase Compound ID GSGSSb3sBFr
InChI InChI=1S/C28H25N3O7/c1-17-6-10-19(11-7-17)27(32)36-16-25-24(38-28(33)20-12-8-18(2)9-13-20)14-26(37-25)30-22-4-3-5-23(31(34)35)21(22)15-29-30/h3-13,15,24-26H,14,16H2,1-2H3/t24-,25+,26+/m1/s1
InChIKey LDENGGSMXNEWEK-ZNZIZOMTSA-N
Mol Weight 515.52 g/mol
Molecular Formula C28H25N3O7
Exact Mass 515.16925 g/mol
Enantiomer InChIKey LDENGGSMXNEWEK-JIMJEQGWSA-N

View Spectrum of 1-[2'-DEOXY-3',5'-BIS-O-(4-METHYLBENZOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-4-NITRO-1H-INDAZOLE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
7-METHOXY-1-[2'-DEOXY-3',5'-DI-O-(PARA-TOLUOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-1H-1,2,3-TRIAZOLO-[4,5-D]-PYRIMIDINE
7-AMINO-3-[2'-DEOXY-3',5'-DI-O-(PARA-TOLYL)-ALPHA-D-ERYTHRO-PENTOFURANOSYL]-3H-1,2,3-TRIAZOLO-[4,5-D]-PYRIMIDINE
7-AMINO-3-[2'-DEOXY-3',5'-DI-O-(PARA-TOLUOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-3H-1,2,3-TRIAZOLO-[4,5-D]-PYRIMIDINE
7-[2'-DEOXY-3',5'-DI-O-(PARA-TOLUOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-4-(METHYLAMINO)-7H-PYRROLO-[2,3-D]-PYRIMIDINE
7-[2'-DEOXY-3',5'-DI-O-(PARA-TOLUOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-4-(METHYLTHIO)-7H-PYRROLO-[2,3-D]-PYRIMIDINE
2-Amino-4-chloro-7-(2-deoxy-3,5-di-O-[4-toluoyl]-B-erythro-pentofuranosyl)-7H-pyrrolo(2,3-D)pyrimidine
6-(HYDROXYMETHYL)-9-(2-DEOXY-3,5-DI-O-TOLUOYL-BETA-D-ERYTHRO-PENTOFURANOSYL)-PURINE
7-[2-DEOXY-5-O-(4,4'-DIMETHOXYTRIPHENYL)-METHYL-BETA-D-ERYTHRO-PENTOFURANOSYL]-4-ISOBUTYRYLAMINO-7H-PYRAZOLO-[3,4-D]-[1,2,3]-TRIAZINE
(Z)-1-[2-DEOXY-3,5-BIS-O-(4-METHYLBENZOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-5-(PHENYLMETHYLENE)-2,4-IMIDAZOLIDINEDIONE
(Z)-1-[2-DEOXY-3,5-BIS-O-(4-METHYLBENZOYL)-ALPHA-D-ERYTHRO-PENTOFURANOSYL]-5-(PHENYLMETHYLENE)-2,4-IMIDAZOLIDINEDIONE
Title Journal or Book Year
Stereoselective Synthesis of Indazole 2′‐Deoxy‐β‐D‐ribonucleosides: Glycosylation of the Nucleobase Anion Helvetica Chimica Acta 1991
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