Recherche de Sous-structure

615867

CCOC(/C=C/B1OC(C)(C)C(C)(C)O1)OCC
Reaction #45472
title compound
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45473
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1nc2ccccc2n1C
Reaction #45474
title compound
Rendement 36.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)noc12
Reaction #45524
7-[(1E)-3-(diethylamino)prop-1-enyl]-3-(4-phenoxyphenyl)isoxazolo[4,5-c]pyridin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C=CB1OC(C)(C)C(C)(C)O1)OCC
Reaction #922174
DOI: 10.1039/C8SC04228D
CCOC(/C=C/B1OC(C)(C)C(C)(C)O1)OCC
Reaction #1358102
title compound
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #1358103
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1nc2ccccc2n1C
Reaction #1358104
title compound
Rendement 36.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)noc12
Reaction #1358157
7-[(1E)-3-(diethylamino)prop-1-enyl]-3-(4-phenoxyphenyl)isoxazolo[4,5-c]pyridin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(/C=C/c1c(F)cccc1[N+](=O)[O-])OCC
Reaction #1709018
(E)-2-(3,3-diethoxyprop-1-enyl)-1-fluoro-3-nitrobenzene
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(/C=C/c1c(F)cccc1[N+](=O)[O-])OCC
Reaction #1899426
(E)-2-(3,3-diethoxyprop-1-enyl)-1-fluoro-3-nitrobenzene
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(/C=C/c1cnc(N)c2c(Br)csc12)OCC
Reaction #2477814
desired product
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(/C=C/B1OC(C)(C)C(C)(C)O1)OCC
Reaction #2477873
title compound
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #2477874
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1nc2ccccc2n1C
Reaction #2477875
title compound
Rendement 36.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)noc12
Reaction #2477929
7-[(1E)-3-(diethylamino)prop-1-enyl]-3-(4-phenoxyphenyl)isoxazolo[4,5-c]pyridin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1