部分構造検索

10140

O=S(=O)(NCCCCSc1cccc2nccn12)c1cccc2ccccc12
Reaction #5554
desired product
収率 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cccc2c(S(=O)(=O)NC(CCCNC(=O)OCc3ccccc3)C(=O)O)cccc12
Reaction #6463
2d
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1cccc2ccccc12)n1ccc2c(N3CCNCC3)cccc21
Reaction #8414
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+](CCCC)(CCCC)CCCC.O=S([O-])c1cccc2ccccc12
Reaction #43891
Tetrabutylammonium 1-Naphthalene Sulfinate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cccc4ccccc34)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49446
4-(1-naphthalenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
収率 61.1%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1cccc2ccccc12
Reaction #64762
title compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC[C@H]1CC[C@H](CNS(=O)(=O)c2cccc3ccccc23)CC1
Reaction #78812
trans-(4-[ (naphthalene-1-sulfonylamino)-methyl]-cyclohexylmethyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCNS(=O)(=O)c1cccc2ccccc12
Reaction #78885
6(1-naphthalenesulfonyl)aminocaproic acid methyl ester
収率 54.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(NS(=O)(=O)c1cccc2ccccc12)SCCN
Reaction #78888
1-naphthalenesulfonylaminoethylthioethylamine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCNS(=O)(=O)c1cccc2ccccc12
Reaction #78889
5-(1-naphthalenesulfonyl)aminopentylamine
収率 84.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2nc(C(F)(F)F)nc(OS(=O)(=O)c3cccc4ccccc34)c2-c2ccccc2)cc1
Reaction #159850
title compound
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(=O)N(c2cc(NS(=O)(=O)c3cccc4c(N(C)C)cccc34)cc(N3C(=O)C=C(C)C3=O)c2)C1=O
Reaction #163951
5
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCOc1cccc(CN(C)c2cccc3c(N(C)C)cccc23)c1)CCC(=O)OC(C)(C)C
Reaction #179314
DOI: 10.1039/C8SC04228D
Cc1c(C(F)(F)F)noc1NS(=O)(=O)c1cccc2ccccc12
Reaction #180005
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc2c(c1)CCN(S(=O)(=O)c1cccc3ccccc13)C2)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #183596
DOI: 10.1039/C8SC04228D
CCCCN(CCCC)c1cccc2c(S(=O)(=O)NC(CC(=O)O)C(=O)O)cccc12
Reaction #190704
DOI: 10.1039/C8SC04228D
COC(=O)c1cnc(N2CCN(S(=O)(=O)c3cccc4c(N(C)C)cccc34)CC2)s1
Reaction #191126
DOI: 10.1039/C8SC04228D
CCCCc1nc2c(N)nc3ccccc3c2n1CCCCNS(=O)(=O)c1cccc2c(N(C)C)cccc12
Reaction #198746
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCC1CCC(CNS(=O)(=O)c2cccc3ccccc23)CC1
Reaction #209962
DOI: 10.1039/C8SC04228D
O=c1[nH]c2nccc(Oc3cccc(NS(=O)(=O)c4cccc5ccccc45)c3)c2[nH]1
Reaction #243012
DOI: 10.1039/C8SC04228D
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