Поиск подструктуры

294170

CCC(C)(C)c1ccc(OCC(CNC(=O)c2cc(C(=O)NCC(COc3ccc(C(C)(C)CC)cc3)C(C)(C)CC)cc(S(=O)[O-])c2)C(C)(C)CC)cc1.[Na+]
Reaction #4973
solid
Выход 82.8%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)C1(CCCCC1)C(=NOCc1ccccc1)N2
Reaction #9427
5′-bromospiro{cyclohexane-1,3′-[3H]indol}-2′(1′H)-one 2′(O-benzyloxime)
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1
Reaction #9428
desired product
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1F
Reaction #9429
desired product
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)c1
Reaction #9430
desired product
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)c1
Reaction #9431
desired compound
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NO)N3)c1
Reaction #9432
desired product
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)cc(-c2ccc3c(c2)C2(CCCCC2)C(=NO)N3)c1
Reaction #9433
desired product
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=Nc2ccc(-c3cccc(Cl)c3)cc2C12CCCCC2
Reaction #9434
desired product
Выход 130.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)(C)c1ccc(OCCCCNC(=O)c2cc(NS(=O)(=O)c3ccc(O)c(N)c3)c3ccccc3c2O)c(C(C)(C)CC)c1
Reaction #54398
4-(3-Amino-4-hydroxybenzenesulfonamido)-1-hydroxy-N-[4-(2,4-di-tert-pentylphenoxy)butyl]-2-naphthamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Cl)cc2)CCOCC1
Reaction #57802
4-(4-Methyl-tetrahydro-pyran-4-yl)-benzenesulfonyl Chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)CCOCC1
Reaction #57901
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3cccnc3)cc2)CCOCC1
Reaction #57902
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccccn3)cc2)CCOCC1
Reaction #57903
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C(=O)c2cc(Cl)ccc2NS(=O)(=O)c2ccc(C3(C)CCOCC3)cc2)n1
Reaction #57904
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)c2cc(Cl)ccc2NS(=O)(=O)c2ccc(C3(C)CCOCC3)cc2)cn1
Reaction #57905
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncccc1C(=O)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(C2(C)CCOCC2)cc1
Reaction #57906
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@]1(c2ccccc2)C[C@@H]2C[C@H]1CC2O
Reaction #73468
( 87 )
Выход 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2ccncc2)(c2ccc(Cl)cc2)CC1
Reaction #73840
title compound
Выход 0.7%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(C2(c3ccc(-c4cn[nH]c4)cc3)CCNCC2)ccn1
Reaction #73841
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее