بحث البنية الفرعية

CCCCC.CCOCC

C=C(C)C(=O)OCCCCCCCCCCCC.C=CN1CCCC1=O
Reaction #1498
lauryl methacrylate N-vinyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCCCCCCCCCCC
Reaction #4991
Dodecyl Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]1CN1CCOC[C@H]1C(=O)Nc1cc(Cl)cc2c1[nH]c1cnccc12
Reaction #40486
2(R)-[3(S)-(6-Chloro-9H-β-carbolin-8-ylcarbamoyl)-morpholin-4-ylmethyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
المردود 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC1CCCCC1
Reaction #40626
title compound
المردود 72.3%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H](C)C(=O)N[C@H](C(=O)N1CCC[C@H]1COC1Cc2ccccc2C1)C1CCCCC1
Reaction #57345
methylamine
المردود 21.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c(/C=C2\C(=O)Nc3ccc(F)cc32)c(C)c1C(=O)NC1CCC(C(=O)N2CCOCC2)CC1
Reaction #66315
title compound
المردود 32.9%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(Cc2ccccc2)c[nH]n1-c1ccc(S(=O)(=O)N(CCCOCc2ccccc2)C2CCCC2)cn1
Reaction #73529
6-(4-benzyl-5-oxo-2,5-dihydro-1H-pyrazol-1-yl)-N-[3-(benzyloxy)propyl]-N-cyclopentylpyridine-3-sulfonamide
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(Cc2ccccc2)c[nH]n1-c1ccc(S(=O)(=O)N(CCCO)C2CCCC2)cn1
Reaction #73530
6-(4-benzyl-5-oxo-2,5-dihydro-1H-pyrazol-1-yl)-N-cyclopentyl-N-(3-hydroxypropyl)pyridine-3-sulfonamide
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCNCCc1ccc(CC(C)(C)C(=O)O)cc1
Reaction #76091
3-[4-(2-heptylamino-ethyl)-phenyl]-2,2-dimethyl-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccccc2)c2ccccc2)cc1.O=C(OC(c1ccccc1)C(F)(F)C(=O)[O-])C12CC3CC(CC(C3)C1)C2
Reaction #86797
4-tert-butylphenyldiphenyl sulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](OC5CCCOC5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #95326
(24R)-5,7-cholestadiene-3β,24,25-triol 3-tetrahydropyranyl ether
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@H](NC(=O)NC1CCCC1)c1ccccc1
Reaction #155453
(R)-tert-butyl 2-(3-cyclopentylureido)-2-phenylacetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCCC1)N[C@@H](C(=O)O)c1ccccc1
Reaction #155454
(R)-2-(3-cyclopentylureido)-2-phenylacetic acid
المردود 64.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC[C@@H]1CCCN1c1nc(N2CCN(c3ccc(Cl)cc3)CC2)nc2c1S(=O)CC2)N1CCOCC1
Reaction #157300
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](NC(=O)N1CC(=NO)NC[C@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c([N+](=O)[O-])c1.Cl
Reaction #167776
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)c2cc(-c3ccc(O)cc3)nc3c2c(/C=C/c2ccc(C(=O)N4CCCCC4)cc2)nn3C2CCCCO2)CC1
Reaction #169224
title compound
المردود 75.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(/C=C/c2n[nH]c3nc(-c4ccc(O)cc4)cc(C(=O)N4CCNCC4)c23)cc1)N1CCCCC1
Reaction #169225
title compound
المردود 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)N(CCO)CCC1CCCCC1)C(=O)OC(C)(C)C
Reaction #178060
DOI: 10.1039/C8SC04228D
CCn1ncc2c(NC3CCOCC3)c(-c3nc(CC4CCNCC4)no3)cnc21
Reaction #178152
DOI: 10.1039/C8SC04228D
CCOC(C)OC(C)(C)C(F)CCC(COS(=O)(=O)c1ccc(C)cc1)C1CCC2C3CC=C4CC(OC5CCCCO5)CC(OC5CCCCO5)C4(C)C3CCC12C
Reaction #182809
DOI: 10.1039/C8SC04228D
الصفحة 1التالي