بحث البنية الفرعية

7985

CCOC(=O)C12CC1C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(O[Si](C)(C)C(C)(C)C)CC1C(=O)N2
Reaction #46089
14-tert-butoxycarbonylamino-18-(tert-butyl-dimethyl-silanyloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid ethyl ester
المردود 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(O[Si](C)(C)C(C)(C)C)CN2C1=O
Reaction #46090
14-tert-butoxycarbonylamino-18-(tert-butyl-dimethyl-silanyloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(Oc3ccccn3)CN2C1=O
Reaction #46099
14-tert-butoxycarbonylamino-2,15-dioxo-18-(pyridin-2-yloxy)-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
المردود 57.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(Oc3ccc([N+](=O)[O-])cc3)CN2C1=O
Reaction #46100
14-tert-butoxycarbonylamino-18-(4-nitrophenoxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
المردود 44.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCCCN1CCOCC1
Reaction #50077
8-morpholinyloctylamine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCCCCCCCN1CCOCC1
Reaction #50079
12-morpholinyldodecylamine
DOI: 10.6084/m9.figshare.5104873.v1
OCCCCCCCCCCCN1CCCCC1
Reaction #65038
1-hydroxy-11-(N-piperidyl)undecane
المردود 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC[C@H](NC(=O)N[C@@H](CCCCNC(=O)CCCCCCCCCCN(Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #84607
(19S,23S)-tri-tert-butyl 1-(1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)-2-((1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)methyl)-13,21-dioxo-2,14,20,22-tetraazapentacosane-19,23,25-tricarboxylate
المردود 21.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCN(CCCN)CCCN
Reaction #161894
target compound
المردود 103.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@]2(CN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]1CCCCN1C(C)C)C1CCCCC1)C(C)(C)C)C(C)(C)C21CCC1
Reaction #164443
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC[C@H](NC(=O)N[C@@H](CCCCNC(=O)CCCCCCCCCCN(Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #164800
(19S,23 S)-tri-tert-butyl 1-(1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)-2-((1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)methyl)-13,21-dioxo-2,14,20,22-tetraazapentacosane-19,23,25-tricarboxylate
المردود 21.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1ccc(CC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #175271
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(OC(=O)c3ccc(F)cc3)CN2C1=O
Reaction #182480
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCC(=O)N(C)CCOC(=O)c1ccc(C)cc1
Reaction #190883
DOI: 10.1039/C8SC04228D
O=C(O)C1CC(C2CCCCC2)CN1C(=O)CP(=O)(O)CCCCc1ccccc1
Reaction #190894
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCC(CCN2CCC(C(=O)c3cc(Cl)ccc3Cl)CC2)CC1
Reaction #193113
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCC[N+](C)(C)CSC#N
Reaction #194040
DOI: 10.1039/C8SC04228D
COc1ccccc1C1(O)CC(CC#N)CC2CN(C(=O)Cc3ccccc3O)CC21
Reaction #195572
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCN(C)C
Reaction #196823
DOI: 10.1039/C8SC04228D
الصفحة 1التالي