Impliqué dans 35 réactions

C(CI)Cl

Clc1nc(N2CCOCC2)c2nc(I)n(C3CCCCO3)c2n1
Reaction #177258
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCOc1c(I)c(NC(=O)OC(C)(C)C)cc2ccccc12
Reaction #263574
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Clc1nc(N2CCOCC2)c2nc(I)n(C3CCCCO3)c2n1
Reaction #421300
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
OC1(CCn2c(I)nc3c(N4CCOCC4)nc(Cl)nc32)CC1
Reaction #421307
1-(2-(2-chloro-8-iodo-6-morpholino-9H-purin-9-yl)ethyl)cyclopropanol
Rendement 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(O)CCn1c(I)nc2c(N3CCOCC3)nc(Cl)nc21
Reaction #421314
4-(2-chloro-8-iodo-6-morpholino-9H-purin-9-yl)-2-methylbutan-2-ol
Rendement 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(Cn1nc(-c2ccc(Cl)cc2)n(CCCl)c1=O)NCc1ccccc1C(F)(F)F
Reaction #748128
2-[4-(2-chloroethyl)-3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-N-[2-(trifluoromethyl)benzyl]-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cn1c(I)nc2c(N3CCOCC3)nc(Cl)nc21
Reaction #770781
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1cc(OC)c2c(=O)oc(-c3cc(C)c(OCCCl)c(C)c3)cc2c1
Reaction #776627
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1ccccc1OC(c1ccccc1)C1CNCCO1
Reaction #991154
2-[α-(2-methoxy-phenoxy)-benzyl]-morpholine
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_10
COCOc1c(I)c(NC(=O)OC(C)(C)C)cc2ccccc12
Reaction #1106469
24
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
COCOc1cccc(NC(=O)OC(C)(C)C)c1I
Reaction #1106473
[N-(tert-Butyloxycarbonyl)amino]-2-iodo-3-(methoxymethoxy)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
COCOc1cccc(NC(=O)OC(C)(C)C)c1I
Reaction #1219411
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COc1cc(I)c(NC(=O)OC(C)(C)C)cn1
Reaction #1296163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
O=C(Cn1nc(-c2ccc(Cl)cc2)n(CCCl)c1=O)NCc1ccccc1C(F)(F)F
Reaction #1302107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCn1c(I)nc2c(N3CCOCC3C)nc(Cl)nc21
Reaction #1303942
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCc1nc2ccccc2n1-c1nc(N2CCOCC2)c2nc(I)n(C)c2n1
Reaction #1306130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COCOc1c(I)c(NC(=O)OC(C)(C)C)cc2ccccc12
Reaction #1472696
24
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_07
COCOc1cccc(NC(=O)OC(C)(C)C)c1I
Reaction #1472703
[N-(tert-Butyloxycarbonyl)amino]-2-iodo-3-(methoxymethoxy)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_07
O=C(O)c1ccc(OCCCl)cc1
Reaction #1514189
title compound
Rendement 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
O=C(CCCCl)Cc1ccccc1
Reaction #1526941
5-chloro-1-phenylpentan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_11
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