benzyl chloride

CCOC(=O)c1cc2cc(N3CCN(Cc4ccccc4)CC3)ccc2o1
Reaction #1267
ethyl 5-(4-benzyl-1-piperazinyl)benzofuran-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCO[PH](=O)Cc1ccccc1
Reaction #1638
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1c(=O)[nH]c(=O)c2c1ncn2Cc1ccccc1
Reaction #2091
7-Benzyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(COCc2ccccc2)cc1
Reaction #2501
dibenzyl ether
المردود 5.4%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
المردود 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
N#Cc1ccc(OCc2ccccc2)cc1
Reaction #5039
4-benzyloxybenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
c1ccc(Cn2ccc3ccccc32)cc1
Reaction #5688
1-Benzylindole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
c1ccc(Cn2c(-c3ccccc3)cc3ccccc32)cc1
Reaction #5691
1-benzyl-2-phenylindole
المردود 13.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cc2ccccc2n1Cc1ccccc1
Reaction #5693
1-benzyl-2-methylindole
المردود 9.4%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
Cc1ccc2c(ccn2Cc2ccccc2)c1
Reaction #5696
1-benzyl-5-methylindole
المردود 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Fc1ccc2c(ccn2Cc2ccccc2)c1
Reaction #5697
1-benzyl-5-fluoroindole
المردود 14.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OCCOCCOCCOCCOCCOCCOCc1ccccc1
Reaction #6714
16
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCCOCCOCCOCCOCc1ccccc1
Reaction #6722
title compound
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCCOCCOCCOCCOCCOCCOCc1ccccc1
Reaction #6727
16
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCCOCCOCCOCCOCc1ccccc1
Reaction #6734
title compound
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCC(c1cn(Cc2ccccc2)c2ccccc12)c1cn(Cc2ccccc2)c2ccccc12
Reaction #7044
product
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc2ccn(Cc3ccccc3)c2c1
Reaction #7156
N-benzyl-6-nitroindole
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cc(-c2ccc(F)c(C)c2)nn(Cc2ccccc2)c1=O
Reaction #8072
title compound
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
الصفحة 1التالي