部分構造検索

38318

CS[C@@H]1CN(C(=O)c2ccccc2)C[C@H]1N
Reaction #1411
1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C2C3CCC(O3)C12
Reaction #8673
10-Oxa-4-azatricyclo[5.2.1.02,6] decane-3,5-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(CO)C(=O)N1
Reaction #10700
hydroxymethylmaleimide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)C2=C(CCCC2)C1=O)C(C)=O
Reaction #10980
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)C1C(=O)NC(=O)C1C(C(=O)OCc1ccccc1)C3
Reaction #11107
benzyl 9-methoxy-1,3-dioxo-1,2,3,3a,4,5,6,10c-octahydropyrrolo[3,4-c]carbazole-4-carboxylate
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C2CCC3Nc4ccccc4C3=C12
Reaction #11136
tetrahydropyrrolo[3,4-c]carbazole-1,3(2H, 3aH)-dione
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)C1C(=O)NC(=O)C1C(c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)C3
Reaction #11139
4-(3,5-Dinitrophenyl)-9-methoxy-4,5,6,10c-tetrahydropyrrolo[3,4-c]carbazole-1,3(2H,3aH)-dione
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c(n2CCCO[Si](C)(C)C(C)(C)C)CC(c2ccccc2OC)C2C(=O)NC(=O)C12
Reaction #11142
6-(3-{[tert-Butyl(dimethyl)silyl]oxy}propyl)-9-methoxy-4-(2-methoxyphenyl)-4,5,6,10c-tetrahydropyrrolo[3,4-c]carbazole-1,3(2H, 3aH)-dione
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)C1C(=O)NC(=O)C1C(c1c(Cl)cccc1OC)C3
Reaction #11145
4-(2-chloro-6-methoxyphenyl)-9-methoxy-4,5,6,10c-tetrahydropyrrolo[3,4-c]carbazole-1,3(2H,3aH)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4)cc1n2CCO)C(=O)NC3=O
Reaction #11157
6-(2-Hydroxyethyl)-9-methoxy-4-phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4)cc1n2CCCO)C(=O)NC3=O
Reaction #11158
alcohol
収率 23.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCC#N)C(=O)NC3=O
Reaction #11160
nitrile
収率 80.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c3c([nH]c2cc1OCc1ccccc1)CC(c1ccccc1Cl)C1C(=O)NC(=O)C31
Reaction #11218
adduct ( 161 )
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(-c4ccccc4)cc4c(c3c2c1)C(=O)NC4=O
Reaction #11239
( 820 )
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccccc1-c1cc2[nH]c3ccc(OCc4ccccc4)cc3c2c2c1C(=O)NC2=O
Reaction #11243
( 854 )
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)c2oc3c(c2c1)C1C(=O)NC(=O)C1C(c1ccccc1Cl)C3
Reaction #11248
7-Bromo-4-(2-chlorophenyl)-9-methoxy-3a,4,5,10c-tetrahydro-1H-[1]benzofuro[3,2-e]isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C2C(c3ccccc3Cl)Cc3[nH]c4ccc([N+](=O)[O-])cc4c3C12
Reaction #11259
adduct ( 917 )
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(c2ccc(C(F)(F)F)cc2)C(=O)N1
Reaction #40924
title compound
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(CO)C(=O)N1
Reaction #52242
Hydroxy Methylmaleimide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #78020
BOC
DOI: 10.6084/m9.figshare.5104873.v1
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