بحث البنية الفرعية

1105849

CN(C)c1cccc2c(S(=O)(=O)NC(CCCNC(=O)OCc3ccccc3)C(=O)O)cccc12
Reaction #6463
2d
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CCN(C(=O)C(CCCNC(=O)OCc2ccccc2)NS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1
Reaction #6464
3d
المردود 91.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc2ccccc2c1)N1CCN(S(=O)(=O)c2ccccc2[N+](=O)[O-])C(CCCNC(=O)OCc2ccccc2)C1=O
Reaction #8624
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC2CN(S(=O)(=O)c3ccccc3[N+](=O)[O-])C2C1
Reaction #182239
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2CNC2C1
Reaction #213100
DOI: 10.1039/C8SC04228D
COC(=O)C1C2CC(NS(=O)(=O)c3ccc(C)cc3)C(C2)N1C(=O)OC(C)(C)C
Reaction #252995
DOI: 10.1039/C8SC04228D
CCCN(C1CC(C(=O)N2CCOCC2)CN(C(=O)OC(C)(C)C)C1)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #272996
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N(Cc2ccncc2)C(C(=O)NOC(C)(C)C)C2CCN(C(=O)OCCc3cccc4ccccc34)CC2)cc1
Reaction #273411
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N(Cc2ccncc2)C(C(=O)NOC(c2ccccc2)(c2ccccc2)c2ccccc2)C2CCN(C(=O)OCCc3cccc4c3OCO4)CC2)cc1
Reaction #293002
DOI: 10.1039/C8SC04228D
COCCCn1cc(CN(C(=O)C2CC(NCCN3C(=O)c4ccccc4C3=O)CN(C(=O)OC(C)(C)C)C2)C2CC2)c2ccccc21
Reaction #302796
DOI: 10.1039/C8SC04228D
CC(CCCNC(=O)Oc1ccccc1)N(c1cc(Cl)ccc1Cl)S(=O)(=O)c1ccc(Cl)cc1
Reaction #372492
DOI: 10.1039/C8SC04228D
O=C(NCCCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #403130
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC[C@@H]2CN(S(=O)(=O)c3ccccc3[N+](=O)[O-])[C@@H]2C1
Reaction #480986
title compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N(Cc2ccncc2)[C@@H](C(=O)NO)C2CCN(C(=O)OCCc3cccc4ccccc34)CC2)cc1.Cl
Reaction #486524
N-hydroxy-2-(R)-[(4-methoxy-benzenesulfonyl) (4-picolyl)amino]-2- [(N-(2-(1-naphthyl)-ethoxycarbonyl))-4-piperidinyl]acetamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N(Cc2ccncc2)[C@@H](C(=O)NOC(C)(C)C)C2CCN(C(=O)OCCc3cccc4ccccc34)CC2)cc1
Reaction #486525
N-(t-butyloxy)-2-(R)-[(4-methoxybenzenesulfonyl) (4-picolyl)amino]-2-[(N-(2-(1-naphthyl)-ethoxycarbonyl))-4-piperidinyl]acetamide
المردود 72.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N(Cc2ccncc2)[C@@H](C(=O)NOC(c2ccccc2)(c2ccccc2)c2ccccc2)C2CCN(C(=O)OCCc3cccc4c3OCO4)CC2)cc1
Reaction #486526
N-(trityl-oxy)-2-(R)-[(4-methoxybenzenesulfonyl) (4-picolyl)amino]-2-[(N-(2-(2,3-methylenedioxy-phenyl)-ethoxycarbonyl))-4-piperidinyl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N(Cc2ccncc2)[C@@H](C(=O)NO)C2CCN(C(=O)OCCc3cccc4c3OCO4)CC2)cc1.O=C(O)C(F)(F)F
Reaction #486527
N-hydroxy-2-(R)-[(4-methoxybenzenesulfonyl)(4-picolyl)amino]-2-[(N-(2-(2,3-methylenedioxyphenyl)-ethoxycarbonyl))-4-piperidinyl]acetamide trifluoroacetic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1[C@H]2C[C@H]([C@H](NS(=O)(=O)c3ccc(C)cc3)C2)N1C(=O)OC(C)(C)C
Reaction #543950
compound
المردود 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1CC[C@@H](N(OCc2ccccc2)S(=O)(=O)c2ccccc2[N+](=O)[O-])CN1C(=O)OC(C)(C)C
Reaction #602769
(2S,5R)-1-tert-butyl 2-ethyl 5-(N-(benzyloxy)-2-nitrophenylsulfonamido)piperidine-1,2-dicarboxylate
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1CC[C@@H](NOCc2ccccc2)CN1C(=O)OC(C)(C)C
Reaction #602770
(2S,5R)-1-tert-butyl 2-ethyl 5-((benzyloxy)amino)piperidine-1,2-dicarboxylate
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي