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625708

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
Rendimiento 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
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(O)CN2C1=O
Reaction #46091
(4-cyclopropanesulfonylaminocarbonyl-18-hydroxy-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-en-14-yl)-carbamic acid tert-butyl ester
Rendimiento 73.0%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
Rendimiento 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
Rendimiento 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2(Cc3ccccc3)CC2)NC(=O)C2CC(Oc3nccc4ccccc34)CN2C1=O
Reaction #174250
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
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(OC(=O)c3ccc4nccnc4c3)CN2C1=O
Reaction #193648
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(OC(=O)c3ccc(Cl)cc3)CN2C1=O
Reaction #199983
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1COCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(OC(=O)Nc3ccccc3Oc3ccccc3)CN2C1=O
Reaction #204058
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(Oc3nc4ccccc4c4ccccc34)CN2C1=O
Reaction #231821
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCOCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(OC(=O)c3ccc(-c4ccccc4)cc3)CN2C1=O
Reaction #238668
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(OC(=O)c3ccc4c(c3)OCO4)CN2C1=O
Reaction #241374
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(Oc3ccccn3)CN2C1=O
Reaction #243788
DOI: 10.1039/C8SC04228D
CCOC(=O)C12CC1C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(Oc3nccc4cc(OC)c(Br)cc34)CC1C(=O)N2
Reaction #247804
DOI: 10.1039/C8SC04228D
Cc1cc(C(=O)OC2CC3C(=O)NC4(C(=O)NS(=O)(=O)C5CC5)CC4C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N3C2)no1
Reaction #249447
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(Oc3nccc4ccccc34)CN2C1=O
Reaction #255056
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(O)CN2C1=O
Reaction #261280
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(O[Si](C)(C)C(C)(C)C)CN2C1=O
Reaction #264300
DOI: 10.1039/C8SC04228D
CCCC1(S(=O)(=O)NC(=O)C23CC2C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N2CC(Oc4nccc5ccccc45)CC2C(=O)N3)CC1
Reaction #268760
DOI: 10.1039/C8SC04228D
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