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486229

CCCN(CCC)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66279
tert-butyl (1E,4E)-8-bromo-4-(dipropylcarbamoyl)-3H-benzo[b]azepin-2-ylcarbamate
Выход 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N(C)C)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66280
tert-butyl (1E,4E)-8-(4-(dimethylcarbamoyl)phenyl)-4-(dipropylcarbamoyl)-3H-benzo[b]azepin-2-ylcarbamate
Выход 83.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CC[C@@H](O[Si](C)(C)C(C)(C)C)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66282
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4C[C@H](O)[C@@H](O)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66285
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)OCC)cc3)cc2N=C(N)C1
Reaction #66288
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCO[Si](C)(C)C(C)(C)C)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66297
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCO)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CC[C@H](O)C4)cc3)cc2N=C(N)C1
Reaction #66298
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(O)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66301
tert-butyl (1E,4E)-4-(dipropylcarbamoyl)-8-(4-hydroxyphenyl)-3H-benzo[b]azepin-2-ylcarbamate
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCF)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66306
tert-butyl (1E,4E)-8-bromo-4-((3-fluoropropyl)(propyl)carbamoyl)-3H-benzo[b]azepin-2-ylcarbamate
Выход 148.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCF)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #181002
DOI: 10.1039/C8SC04228D
CCCN(CCC)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #199330
DOI: 10.1039/C8SC04228D
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CC(O)C(O)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #398448
DOI: 10.1039/C8SC04228D
CCCN(CCCO[Si](C)(C)C(C)(C)C)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #399981
DOI: 10.1039/C8SC04228D
CCCN(CCC)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #680624
tert-butyl (1E,4E)-8-bromo-4-(dipropylcarbamoyl)-3H-benzo[b]azepin-2-ylcarbamate
Выход 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N(C)C)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #680625
tert-butyl (1E,4E)-8-(4-(dimethylcarbamoyl)phenyl)-4-(dipropylcarbamoyl)-3H-benzo[b]azepin-2-ylcarbamate
Выход 83.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CC[C@@H](O[Si](C)(C)C(C)(C)C)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #680627
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4C[C@H](O)[C@@H](O)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #680630
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)OCC)cc3)cc2N=C(N)C1
Reaction #680633
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCO[Si](C)(C)C(C)(C)C)C(=O)C1=Cc2ccc(Br)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #680642
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCCO[Si](C)(C)C(C)(C)C)C(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CC[C@H](O)C4)cc3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #680643
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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