phosphorus oxychloride

COC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)Cl
Reaction #1092
2-Methoxycarbonyl-5-nitrobenzenesulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C=C(C=O)c1ccc(Cl)cc1
Reaction #1600
2-(4-chlorophenyl)-3-dimethylaminopropenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C=C(C=O)c1ccc(Cl)cc1
Reaction #1667
2-(4-chlorophenyl)-3-dimethylaminopropenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc2c(c1)CCc1c-2c(=O)oc2cc(O)ccc12
Reaction #1805
title compound
المردود 70.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Fc1ccc(Cc2ncc(F)c(Cl)n2)cc1
Reaction #1940
title compound
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
Reaction #2045
5-[N-(4-formylphenyl)-N-phenylamino]acenaphthene
المردود 86.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(N(c2ccc(C=O)cc2)c2ccc3c4c(cccc24)CC3)cc1
Reaction #2050
5-[N-(4-formylphenyl)-N-(4-tolyl)amino]acenaphthene
المردود 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C=C(C=O)c1ccc(Cl)cc1
Reaction #2172
2-(4-chlorophenyl)-3-dimethylaminopropenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C=C(C=O)c1ccc(Cl)cc1
Reaction #2213
2-(4-chlorophenyl)-3-dimethylaminopropenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)c1ccnc(Cl)c1
Reaction #2248
4-acetyl-2-chloro-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1cccc(Nc2nccc(-c3ccnc(Cl)c3)n2)c1
Reaction #2253
N-(3-chloro-phenyl)-4-(2-chloro4-pyridyl)-2-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C=C(C=O)c1ccc(Cl)cc1
Reaction #2271
2-(4-chlorophenyl)-3-dimethylaminopropenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccnc(Cl)c1
Reaction #2834
2-chloroisonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1nccc2sccc12
Reaction #2857
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1cc(C=O)ccc1O
Reaction #3047
desired subtitled intermediate
المردود 22.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1cc(C=O)ccc1O
Reaction #3050
3-(1,1-dimethylethyl)-4-hydroxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1c2cc3c(cc2-c2c1c(Cl)nc1ccccc21)OCO3
Reaction #3245
title compound
المردود 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc2c3c(c(Cl)nc2c1)C(=O)c1ccccc1-3
Reaction #3248
title compound
المردود 73.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1c2ccccc2-c2c1nc(Cl)c1ccccc21
Reaction #3250
title compound
المردود 78.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1ncc(C#N)c(Cl)n1
Reaction #3256
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
الصفحة 1التالي