P2O5

CCCCCCCCCCCCCCOCC(O)CNCCOP(=O)([O-])O.[Na+]
Reaction #1202
title compound
المردود 36.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCn1c(-c2ccccc2)nc(C(F)(F)F)cc1=O
Reaction #1551
3-methoxymethyl-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
المردود 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCc2ccccc2N1
Reaction #1829
product
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P([O-])([O-])OP(=O)([O-])[O-].[Ti+4]
Reaction #3152
titanium pyrophosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P([O-])([O-])OP(=O)([O-])[O-].[Ti+4]
Reaction #3153
titanium pyrophosphate
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCC[N+](C)(C)C.C[O-]
Reaction #4828
octyltrimethyl ammonium methoxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC1(C)CCSc2ccccc21
Reaction #6629
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(CC(=O)c2sc(-c3ccc(C(F)(F)F)cc3)cc2C)cc1C
Reaction #9763
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=Cc1nc2cc(Br)ccc2o1
Reaction #10501
5-bromo-2-vinyl-benzooxazole
المردود 45.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CCCN1CCc1nc2cc(Br)ccc2[nH]1
Reaction #10512
title compound
المردود 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCOc1cnc(C(=O)OCC)o1
Reaction #46265
title material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1Nc2ccc(F)cc2C(O)(c2ccccc2)N1CC(F)(F)F
Reaction #47956
6-fluoro-4-hydroxy-4-phenyl-3-(2,2,2-trifluoroethyl)-3,4-dihydroquinazolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO
Reaction #51519
title compound
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(NC(=O)c4ccccc4)ncnc32)O[C@@H]1CO
Reaction #51520
title compound
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(NC(=O)c4ccccc4)ncnc32)O[C@@H]1CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #51521
title compound
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)[Si](C)(C)C(O)CO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO
Reaction #51525
3′-O (2-tert-butyldimethylsilylhydroxyethyl)adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC1C=CC(C)C(C=O)O1
Reaction #56361
3,6-dihydro-3-methyl-6-ethoxy-2H-pyran-2-carboxaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=c1[nH]nc(Cc2ccc([N+](=O)[O-])cc2)o1
Reaction #58925
5-(4-nitrobenzyl)-1,3,4-oxadiazol-2(3H)-one
المردود 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1cnc(-c2ccccc2)c1-c1nc2c(N)ncnc2[nH]1
Reaction #60790
title compound
المردود 96.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Nc1ncnc2[nH]c(-c3[nH]cnc3-c3ccccc3)nc12
Reaction #60818
title compound
المردود 6.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
الصفحة 1التالي