ammonium persulphate

—
Reaction #449936
Azomethine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
N#Cc1ccnc(CO)c1
Reaction #452178
4-cyano-2-hydroxymethylpyridine
收率 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
CN(C)Cc1ccnc(CO)c1
Reaction #452180
4-dimethylaminomethyl-2-hydroxymethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
CN(C)Cc1ccnc(CCCC#N)c1
Reaction #452183
2-(3-cyanopropyl)-4-dimethylaminomethylpyridine
收率 36.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
C=CC(=O)O.C=CC(N)=O
Reaction #459085
Acrylamide Acrylic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
O=C([O-])CCC(=O)OP(=O)(O)OC(=O)CCC(=O)[O-].[Na+].[Na+]
Reaction #459141
Sodium phosphinico bis succinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
O=C(O)c1cc(F)c(F)cc1Cl
Reaction #461795
2-chloro-4,5-difluorobenzoic acid
收率 80.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
Clc1cc(C23CCC(CC2)C3)c(Cl)nn1
Reaction #467499
title compound
收率 98.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC1=CCC(CC(C)C)([I+]c2ccccc2)C=C1.F[P-](F)(F)(F)(F)F
Reaction #468386
p-isobutylphenyl-p-tolyl-iodonium hexafluorophosphate
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC(C)(CO)c1cc(Cl)nnc1Cl
Reaction #501390
3,6-dichloro-4-(1-hydroxymethyl-1-methylethyl)pyridazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC(C)(CO)c1cc(Cl)nnc1Cl
Reaction #501391
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CCC(CC)(CO)c1cc(Cl)nnc1Cl
Reaction #501392
3,6-dichloro-4-(1-ethyl-1-hydroxymethylpropyl)pyridazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC(C)c1cc(Cl)nnc1Cl
Reaction #501394
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC(C)(C)c1cc(Cl)nnc1Cl
Reaction #501395
3,6-dichloro-4-t-butylpyridazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC1(c2cc(Cl)nnc2Cl)CC1(Cl)Cl
Reaction #501397
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
—
Reaction #507605
sulfuric acid ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=C(COCC(C)C)C(N)=O
Reaction #514004
solution
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_10
CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2c-1nc1ccccc1c2CO
Reaction #521983
7-hydroxymethylcamptothecin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2c-1nc1ccccc1c2CO
Reaction #521985
7-hydroxymethylcamptothecin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #526852
compound XI
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
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