5′-O-tert-butyldiphenylsilyl-2′-O-[N,N-dimethylaminooxyethyl]-5-methyluridine

Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #11302
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #51518
title compound
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #51590
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #52149
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #60561
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #78377
2′—O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #316819
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #362834
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #363933
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #409085
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #436344
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #439207
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #440205
2′-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #453124
106
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #453477
2'-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #454166
2'-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #454167
2'-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #454204
2'-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #456107
2'-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCON(C)C)c(=O)[nH]c1=O
Reaction #456756
2'-O-(dimethylaminooxyethyl)-5-methyluridine
収率 92.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
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