بحث البنية الفرعية

9696

CCCC[C@H](O[C@@H](Cc1ccccc1)C(=O)OC(c1ccccc1)c1ccccc1)c1ccco1
Reaction #5658
(2S,4S) Benzhydryl 2-Benzyl-4-(2-furyl)-3-oxaoctanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@H](O[C@H](Cc1ccccc1)C(=O)OC(c1ccccc1)c1ccccc1)c1ccco1
Reaction #5659
(2R,4S) benzhydryl 2-Benzyl-4-(2-furyl)-3-oxaoctanoate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)c2ccccc2)CCN1C(=O)C(C#N)c1nc2ccccc2s1
Reaction #7695
(R)-N-(benzoyl)-3-methyl-N′-[(benzothiazol-2-yl)-2-cyanoacetyl]-piperazine
المردود 6.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2sc(C(=N)C(C#N)N3CCN(C(=O)c4ccccc4)C[C@H]3C)nc2c1
Reaction #7696
(R)-N-(benzoyl)-3-methyl-N′-[2-(5-methoxy-benzothiazol-2-yl)-2-imino-1-cyano-ethyl]-piperazine
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(c2ccc(-c3nc4ccccc4o3)cc2Cl)CCCC1
Reaction #7815
1-[4-(1,3-benzoxazol-2-yl)-2-chlorophenyl]cyclopentanecarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nc3ccccc3o2)ccc1C1(C#N)CCCC1
Reaction #7830
1-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]cyclopentanecarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1cncc(Br)c1
Reaction #9478
3-bromo-5-ethoxymethylpyridine
المردود 120.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)c1cn(C(=O)OC(C)(C)C)c2ccccc12
Reaction #40497
3-(cyano-methyl-methyl)-indole-1-carboxylic acid tert-butyl ester
المردود 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H]1OC(=O)[C@]1(CCCC)C(=O)OCc1ccccc1
Reaction #42001
β-lactone
المردود 76.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC1CCCC(O)CCC1
Reaction #44488
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(CN4CCC(F)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45007
title compound
المردود 16.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3cnc(N4CCN(C)CC4)cn3)[nH]n2)cc(OC)c1
Reaction #45010
product
المردود 45.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(OCCO)cc3)n[nH]2)cc(OC)c1
Reaction #45018
title compound
المردود 12.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(CC(C)N)cc3)n[nH]2)cc(OC)c1
Reaction #45019
title compound
المردود 4.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(CN4CCCC(F)C4)cc3)n[nH]2)cc(OC)c1
Reaction #45020
title compound
المردود 16.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3ccc(N4CCN(C)CC4)cn3)[nH]n2)cc(OC)c1
Reaction #45028
title compound
المردود 67.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3cnc(N4CCN(C)CC4)nc3)n[nH]2)cc(OC)c1
Reaction #45035
title compound
المردود 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(N4CC(C)NC(C)C4)cc3)[nH]n2)cc(OC)c1
Reaction #45041
title compound
المردود 10.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN(C)C(C)C4)cc3)n[nH]2)cc(OC)c1
Reaction #45043
title compound
المردود 19.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccccc3NCc3cc(C)no3)n[nH]2)cc(OC)c1
Reaction #45046
title compound
المردود 10.5%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي