pyridine DCM

COc1ccc(C(OC[C@@]23CO[C@@H]([C@H](n4cc(C)c(=O)[nH]c4=O)O2)[C@H]3OCc2ccccc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #6876
nucleoside
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)N1CCC(C)C(N(C)c2ncnc3[nH]ccc23)C1
Reaction #8800
title compound
Rendimiento 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)N1CCC(C)C(N(C)c2ncnc3[nH]ccc23)C1
Reaction #72693
title compound
Rendimiento 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCN(C(C)C)C(C)C
Reaction #76249
Hünig's base
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCNC(=O)N1CCCCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162062
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@@H]1CN(c2ccc(Cl)c(NS(=O)(=O)c3ccc(Br)cc3)c2)C[C@H](C)N1
Reaction #217605
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C[C@@H]1CN(c2ccc(Cl)c(NS(=O)(=O)c3ccc(Br)s3)c2)C[C@H](C)N1
Reaction #217606
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1ccc(NS(=O)(=O)c2ccc(-c3cccs3)cc2)cc1N1C[C@@H](C)N[C@@H](C)C1
Reaction #217616
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCC(=O)Nc1cc(-c2nc(-c3ccc(C(=O)OC)c(F)c3)no2)ccc1N1CCCCC1C
Reaction #307130
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(=O)N[C@H]1[C@@H](OCc2ccccc2)O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@@H]1OCC(COC(C)=O)OC(C)=O
Reaction #330933
crystalline compound 10
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=CCO[C@@H]1[C@@H](NC(C)=O)[C@@H](OCc2ccccc2)O[C@H](COCc2ccccc2)[C@H]1O[C@]1(N)O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1C(=O)OCC(Cl)(Cl)Cl
Reaction #330935
14
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1cc(C(=O)N2CCC(CCOC(C)=O)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #410400
1-(3,4,5-trimethoxybenzoyl)-3-(3,4-dichlorophenyl)-3-(2-acetoxyethyl)pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCCCCCCC/C=C\CCCCCCCCOCC(COS(=O)(=O)NCCN(C)C)OCCCCCCCC/C=C\CCCCCCCC
Reaction #463607
title compound
Rendimiento 18.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
COC(CN(Cc1ccc(Br)cc1)S(=O)(=O)c1ccc(C)cc1)OC
Reaction #491897
title compound
Rendimiento 63.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Cc1c(C#N)sc2ncnc(Nc3ccc(F)cc3OC3CCOCC3)c12
Reaction #537765
title compound
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCC(=O)NCC1Cc2ccc(NS(=O)(=O)c3ccc(C(C)C)cc3)cc2C1
Reaction #537912
product
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCC(=O)NCC1Cc2cccc(NS(=O)(=O)c3ccc(C(C)C)cc3)c2C1
Reaction #537914
product
Rendimiento 101.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1c(C(=O)Nc2ccc(Oc3ccnc(NC(=O)Oc4ccccc4)c3)c(F)c2)c(=O)n(-c2ccccc2)n1C
Reaction #607897
title compound
Rendimiento 57.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(Oc3ccnc(NC(=O)Oc4ccccc4)c3)cc2)c(=O)n(-c2ccccc2)n1C
Reaction #607907
title compound
Rendimiento 42.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCCNC(=O)N1CCCC(Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #614069
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
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