18-crown-6

OCCOc1ccccc1-c1cccc2c1-c1ccccc1C2
Reaction #885
white powder
Rendimiento 970.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1ccc(N(c2ccccc2)c2ccc(N(c3ccccc3)c3ccc(Cl)cc3)cc2)cc1
Reaction #2421
grey-white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc2cc(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(OCc3ccccc3)cc2o1
Reaction #2785
7-benzyloxy-6-D-glucopyranosyloxycoumarin
Rendimiento 86.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(OCc2ccccc2)cc(=O)o1
Reaction #3005
4-Benzyloxy-6-methyl-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1ccc2c(ccn2Cc2ccccc2)c1
Reaction #5692
1-benzyl-5-chloroindole
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cc2ccccc2n1Cc1ccccc1
Reaction #5694
1-benzyl-2-methylindole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCn1ccc2ccccc21
Reaction #5695
1-allylindole
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Fc1ccc2c(ccn2Cc2ccccc2)c1
Reaction #5697
1-benzyl-5-fluoroindole
Rendimiento 14.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCN(CC(=O)O)c1ccc(F)cc1
Reaction #5914
Ethyl N-(4-fluorophenyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)[Si](Oc1ccc2c(c1)c1c(n2C)CN(C(=O)OC(C)(C)C)CC1)(C(C)C)C(C)C
Reaction #6843
9-methyl-6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-β-carboline-2-carboxylic acid tert-butyl ester
Rendimiento 41.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CSc1nccc(F)n1
Reaction #9856
4-fluoro-2-methylthiopyrimidine
Rendimiento 63.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #10887
1-cyclopentyl-4-(4-nitrophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)CN1CCN(c2ccc([N+](=O)[O-])cc2)CC1
Reaction #10889
1-(isobutyl)-4-(4-nitrophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(Cl)cc1CC#N
Reaction #11745
title compound
Rendimiento 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cccnc1-n1cnc(-c2ccccc2)c1
Reaction #40703
dark oil
Rendimiento 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1cccnc1-n1cc(-c2ccccc2)cn1
Reaction #40706
oil
Rendimiento 79.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1c(CC=O)cccc1[N+](=O)[O-]
Reaction #44141
title compound
Rendimiento 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(-c2csc3c(N=C(c4ccccc4)c4ccccc4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45510
title compound
Rendimiento 64.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Oc1cccc(C=C[N+](=O)[O-])c1
Reaction #48623
desired compound
Rendimiento 987.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccccc1-c1cn2c(F)nc3c(c2n1)CCCC3
Reaction #50293
Compound 41
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
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