بحث البنية الفرعية

CCCCCI

CCCCCCOc1cc2ccc(-c3ccc(C(=O)OC)c(O)c3)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1230
methyl 2-hydroxy-4-[7-(1-adamantyl)-6-hexyloxy-2-naphthyl]benzoate
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCCCCCCCCCCOc1ccc(C(=O)O)cc1
Reaction #5259
4-(10-allyloxydecyloxy)benzoic acid
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #10887
1-cyclopentyl-4-(4-nitrophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCI)CCc4cc(F)ccc43)c[nH]c12
Reaction #41996
title compound
المردود 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCCC1(c2c[nH]c3c(NS(C)(=O)=O)cccc23)CCc2cc(F)ccc21
Reaction #41997
title compound
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCN4CCOCC4)CCc4cc(F)ccc43)c[nH]c12
Reaction #41998
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c([C@H]2CC[C@@H](O)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45868
compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@](O)(c2ccc(Cl)c(Cc3ccc(OC4CCCC4)cc3)c2)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #48104
1-Chloro-2-(4-cyclopentyloxybenzyl)-4-(β-D-glucopyranos-1-yl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCC1CCC(CN(Cc2ccccc2)S(=O)(=O)NC(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1
Reaction #52014
title compound
المردود 73.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCN(C(=O)C(C)C)c1sc(CC)cc1C(=O)OCC
Reaction #55940
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CCCC(C)C
Reaction #56727
2,2,6-Trimethyl-heptanoic acid methyl ester
المردود 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN1C(=O)C2CC(c3ccc([N+](=O)[O-])cc3)(C2)C1=O
Reaction #63370
1-(4-nitrophenyl)-3-n-pentyl-3-azabicyclo[3.1.1]heptane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOc1ccc2[nH]c(C)c(CC(=O)O)c2c1
Reaction #65985
white crystals
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)C)n(Cc3ccccc3)c2c1
Reaction #68319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCCC3)cc2n1Cc1ccccc1
Reaction #68321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(C(F)(F)F)nc2)c2ccc(OC3CCCC3)cc2n1Cc1ccccn1
Reaction #68412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2cncc(F)c2)c2ccc(OC3CCCC3)cc2n1Cc1cccnc1
Reaction #68419
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
المردود 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
المردود 64.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81467
17-(3-Pyridyl)androsta-5,16-dien-3β-ol
DOI: 10.6084/m9.figshare.5104873.v1
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