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1407230

C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(C)(O)CC1)c1ccccc1
Reaction #46638
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN([C@@H](C(=O)O)c2ccccc2)CC1
Reaction #46639
title compound
収率 98.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(O)(c2ccccc2)CC1)c1ccccc1
Reaction #46643
title compound
収率 27.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C2CC(OC(=O)c3c[nH]c4ccccc34)CC1CC(C(=O)OC)C2
Reaction #48480
7-(1H-Indole-3-carbonyloxy)-9-methoxycarbonylmethyl-9-aza-bicyclo[3.3.1]nonane-3-carboxylic acid methyl ester
収率 89.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(=O)C2CC3CC(OC(=O)c4c[nH]c5ccccc45)CC(C2)N31
Reaction #48481
5-(1H-Indole-3-carbonyloxy)-10-oxo-8-aza-tricyclo[5.3.1.03,8]undecane-9-carboxylic acid methyl ester
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CC2CC3CC(C1)N2CC3=O)c1c[nH]c2ccccc12
Reaction #48482
1H-Indole-3-carboxylic acid 10-oxo-8-aza-tricyclo[5.3.1.03,8]undec-5-yl ester
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)CN2CCC(O)CC2)C(=O)OCc2ccccc2)cc1
Reaction #87095
(S)-benzyl 2-((S)-2-(2-(4-hydroxypiperidin-1-yl)acetamido)propanamido)-3-(4-methoxyphenyl)propanoate
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN(CC(=O)O)CC1
Reaction #87161
2-(4-hydroxy-4-methylpiperidin-1-yl)acetic acid
収率 89.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCC(O)CC1)OCc1ccccc1
Reaction #87171
benzyl 2-(4-hydroxypiperidin-1-yl)acetate
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1CCC(O)CC1
Reaction #87172
2-(4-hydroxypiperidin-1-yl)acetic acid
収率 94.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(C)(O)CC1)c1ccccc1
Reaction #155444
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN([C@@H](C(=O)O)c2ccccc2)CC1
Reaction #155445
title compound
収率 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCC(O)(c2ccc(-c3ccc(Nc4ccc(C(F)(F)F)nc4)nc3)cc2)CC1
Reaction #163234
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1CCC(O)(c2ccc(-c3ccc(Nc4ccc(C(F)(F)F)nc4)nc3)cc2)CC1
Reaction #163235
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCC(Oc2ccccc2)CC1)Nc1ccc2[nH]c(=O)oc2c1
Reaction #176083
DOI: 10.1039/C8SC04228D
CCOC(=O)CN1C(C)(C)CC(OCc2ccccc2)CC1(C)C
Reaction #233830
DOI: 10.1039/C8SC04228D
O=C(OC1CC2CC3CC(C1)N2CC3=O)c1c[nH]c2ccccc12
Reaction #241059
DOI: 10.1039/C8SC04228D
O=C1Cc2cc(NC(=O)C(=O)N3CCC(Oc4ccc(F)cc4)CC3)ccc2N1
Reaction #248705
DOI: 10.1039/C8SC04228D
Cc1ccc(OC2CCN(C(=O)C(=O)Nc3ccc4[nH]c(=O)[nH]c4c3)CC2)cc1
Reaction #265868
DOI: 10.1039/C8SC04228D
COC(=O)C(c1ccccc1Cl)N1CCC(OS(C)(=O)=O)C(=CC(=O)N(C)C)C1
Reaction #267882
DOI: 10.1039/C8SC04228D
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