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O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3

CCCCCCCCCCCCCCOCC(O)CNCCOP(=O)([O-])O.[Na+]
Reaction #1202
title compound
Ausbeute 36.2%DOI: 10.6084/m9.figshare.5104873.v1
COCn1c(-c2ccccc2)nc(C(F)(F)F)cc1=O
Reaction #1551
3-methoxymethyl-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2ccccc2N1
Reaction #1829
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])([O-])OP(=O)([O-])[O-].[Ti+4]
Reaction #3152
titanium pyrophosphate
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])([O-])OP(=O)([O-])[O-].[Ti+4]
Reaction #3153
titanium pyrophosphate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
Reaction #3844
P2O5
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[N+](C)(C)C.C[O-]
Reaction #4828
octyltrimethyl ammonium methoxide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCSc2ccccc21
Reaction #6629
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(=O)c2sc(-c3ccc(C(F)(F)F)cc3)cc2C)cc1C
Reaction #9763
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1nc2cc(Br)ccc2o1
Reaction #10501
5-bromo-2-vinyl-benzooxazole
Ausbeute 45.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN1CCc1nc2cc(Br)ccc2[nH]1
Reaction #10512
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCNC(=O)c2[nH]ccc21
Reaction #42649
aldisine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Oc1ccc(-c2ncco2)cc1
Reaction #44777
4-(oxazol-2-yl)phenyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Ic1ccc(-c2ncco2)cc1
Reaction #44783
2-(4-iodophenyl)oxazole
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1cnc(C(=O)OCC)o1
Reaction #46265
title material
DOI: 10.6084/m9.figshare.5104873.v1
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.v1
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO
Reaction #51519
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(NC(=O)c4ccccc4)ncnc32)O[C@@H]1CO
Reaction #51520
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
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
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
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