AlCl3

CSc1ccc(C(C)=O)cc1
Reaction #1160
4-(methylthio)acetophenone
المردود 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1ccc(-c2ccc(C(C)(C)C)c(O)c2)cc1
Reaction #1175
2-tert-butyl-5-(4'-tert-butylphenyl) phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CC1Cc2c(Br)cccc2C1=O
Reaction #1358
4-bromo-2-i-butyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #1591
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
المردود 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #1597
3(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc2c(Cl)cccc2[nH]1
Reaction #1604
5-chloro-2-quinolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #1658
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
المردود 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #1664
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc2c(Cl)cccc2[nH]1
Reaction #1672
5-chloro-2-quinolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc2c(c1)CN(c1ccc(OCCN3CCCCC3)cc1)c1c-2ccc2cc(O)ccc12
Reaction #1807
title compound
المردود 60.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1Nc2ccc(Cl)cc2C1(c1ccccc1)c1ccccc1
Reaction #1911
5-Chloro-1,3-dihydro-3,3-diphenylindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCc1c(CC[Si](Cl)(Cl)Cl)c(CC[Si](Cl)(Cl)Cl)c(CC[Si](Cl)(Cl)Cl)c(CC[Si](Cl)(Cl)Cl)c1CC[Si](Cl)(Cl)Cl
Reaction #1930
pentakis(trichlorosilylethyl)-n-butylbenzene
المردود 102.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #2163
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
المردود 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #2169
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc2c(Cl)cccc2[nH]1
Reaction #2177
5-chloro-2-quinolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #2204
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
المردود 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #2210
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc2c(Cl)cccc2[nH]1
Reaction #2218
5-chloro-2-quinolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ccc2c(Cl)cccc2[nH]1
Reaction #2276
5-chloro-2-quinolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2cccc3ccccc23)sc2cc(O)ccc12
Reaction #2288
title product
المردود 53.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
الصفحة 1التالي