部分構造検索

14889

Cc1cc2c(C(=O)OCc3ccccc3)cccc2[nH]1
Reaction #11503
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(C(=O)n2c(C)cc3c(C(=O)OCc4ccccc4)cccc32)cc1
Reaction #11504
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3[nH]c(C)cc3c2C(=O)OCc2ccccc2)n1
Reaction #80288
desired product
収率 85.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3[nH]c(C)c(C=O)c3c2C(=O)OCc2ccccc2)n1
Reaction #80289
desired compound
収率 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)n(C(=O)c2ccccc2)c2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)OCc3ccccc3)c12
Reaction #80294
desired compound
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)n(C(=O)c2ccccc2)c2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)O)c12
Reaction #80295
desired compound
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)n(C(=O)c2ccccc2)c2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)O)c12
Reaction #175958
DOI: 10.1039/C8SC04228D
COc1cc(OC)nc(Oc2ccc3[nH]c(C)cc3c2C(=O)OCc2ccccc2)n1
Reaction #234229
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C(=O)O)cccc2n1C(=O)OC(C)(C)C
Reaction #245636
DOI: 10.1039/C8SC04228D
COc1cc(OC)nc(Oc2ccc3[nH]c(C)c(C=O)c3c2C(=O)OCc2ccccc2)n1
Reaction #295725
DOI: 10.1039/C8SC04228D
Cc1cc2c(C(=O)OCc3ccccc3)cccc2[nH]1
Reaction #438823
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(=O)OCc3ccccc3)cccc2n1C(=O)OC(C)(C)C
Reaction #516798
benzyl 1-tert-butoxycarbonyl-2-ethoxycarbonylindole-4-carboxylate
収率 16.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(=O)O)cccc2n1C(=O)OC(C)(C)C
Reaction #516803
1-tert-butoxycarbonyl-2-ethoxycarbonylindole-4-carboxylic acid
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1cc2c(C(=O)OCc3ccccc3)cccc2[nH]1)(c1ccccc1)c1ccccc1
Reaction #516826
benzyl 2-tert-butyldiphenylsilyloxymethylindole-4-carboxylate
収率 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(CN2C(=O)c3ccccc3C2=O)cc2c(C(=O)OCc3ccccc3)cccc21
Reaction #516844
benzyl 1-tert-butoxycarbonyl-2-phthalimidomethylindole-4-carboxylate
収率 70.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)n(C(=O)c2ccccc2)c2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)OCc3ccccc3)c12
Reaction #923934
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C(=O)OCc3ccccc3)cccc2n1C(=O)OC(C)(C)C
Reaction #1620930
benzyl 1-tert-butoxycarbonyl-2-ethoxycarbonylindole-4-carboxylate
収率 16.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(=O)O)cccc2n1C(=O)OC(C)(C)C
Reaction #1620934
1-tert-butoxycarbonyl-2-ethoxycarbonylindole-4-carboxylic acid
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1cc2c(C(=O)OCc3ccccc3)cccc2[nH]1)(c1ccccc1)c1ccccc1
Reaction #1620952
benzyl 2-tert-butyldiphenylsilyloxymethylindole-4-carboxylate
収率 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(CN2C(=O)c3ccccc3C2=O)cc2c(C(=O)OCc3ccccc3)cccc21
Reaction #1620971
benzyl 1-tert-butoxycarbonyl-2-phthalimidomethylindole-4-carboxylate
収率 70.8%DOI: 10.6084/m9.figshare.5104873.v1
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