部分構造検索

1015379

COCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #469418
product
収率 124.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](C=Cc2ccccc2)[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #535845
5′-O-(tert-butyldiphenylsilyl)-3′-deoxy-2′-O-(2-methoxyethyl)-3′-(2-phenylethenyl)-5-methyluridine
収率 13.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]([C@@H](C)O)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #965070
Compound 11
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](O)[C@@H]([C@@H](C)OC(c2ccccc2)(c2ccc(OC)cc2)c2ccc(OC)cc2)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #965071
Compound 12
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[NH+](CC)CC.CC[NH+](CC)CC.COCCO[C@@H]1[C@H](OC(CC(=O)[O-])C(=O)[O-])[C@@H](COC(c2ccccc2)(c2ccc(OC)cc2)c2ccc(OC)cc2)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #978404
solid
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](O)[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #1255769
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #1255770
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](C=Cc2ccccc2)[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #1332682
5′-O-(tert-butyldiphenylsilyl)-3′-deoxy-2′-O-(2-methoxyethyl)-3′-(2-phenylethenyl)5-methyluridine
収率 13.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](C=Cc2ccccc2)[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #1357420
5′-O-(tert-butyldiphenylsilyl)-3′-deoxy-2′-O-(2-methoxyethyl)-3′-(2-phenylethenyl)5-methyluridine
収率 13.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](C=Cc2ccccc2)[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #1923400
5′-O-(tert-butyldiphenylsilyl)-3′-deoxy-2′-O-(2-methoxyethyl)-3′-(2-phenylethenyl)5-methyluridine
DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #2173719
product
収率 124.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](O)[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #2273617
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #2273618
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCO[C@@H]1[C@H](C=Cc2ccccc2)[C@@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Reaction #2300078
5′-O-(tert-butyldiphenylsilyl)-3′-deoxy-2′-O-(2-methoxyethyl)-3′-(2-phenylethenyl)5-methyluridine
収率 13.6%DOI: 10.6084/m9.figshare.5104873.v1