H3PO2

O=[PH](O)CCCOCc1ccccc1
Reaction #1626
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCC[PH](=O)O
Reaction #1633
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(C[Se]CC(N)c1ccccc1)c1ccccc1
Reaction #3997
Phenyl-2-aminoethyl selenide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(Oc1ccccc1)Oc1ccccc1
Reaction #50130
diphenyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(C)C(NC(c1ccccc1)c1ccccc1)P(O)O
Reaction #54251
1-benzhydrylamino-2-methylpropanephosphonous acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CSc1nccc(-c2cc3cn[nH]c3nc2-c2ccc(F)cc2)n1
Reaction #70884
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cc(C)cc(Br)c1
Reaction #72249
title compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Oc1c(-c2ccccc2)cccc1C(c1ccccc1)c1cccc(-c2ccccn2)c1
Reaction #73715
A1
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)c1cccc(C(c2ccccc2)c2cccc(-c3ccccn3)c2)c1O
Reaction #73721
A3
Ausbeute 19.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccccc1-c1cccc(C(c2ccccc2)c2cccc(-c3ccccc3)c2OCc2ccccc2)c1
Reaction #73740
D2
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccccc1-c1cccc(C(c2ccccc2)c2cccc(C(C)(C)C)c2O)c1
Reaction #73745
D4
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1scnc1C(=O)OC
Reaction #155467
methyl 5-ethylthiazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Brc1cccc2c1ccc1ccccc12
Reaction #155686
1-bromophenanthrene
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Brc1cccc2c1ccc1ccccc12
Reaction #155703
1-bromophenanthrene
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Brc1cccc2c1ccc1ccccc12
Reaction #155714
1-bromophenanthrene
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1cc(-c2ccc3ncc(Cc4ccc5ncccc5c4)n3n2)cn1
Reaction #156337
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1cc(-c2ccc3ncc(Cc4ccc5nccn5c4)n3n2)cn1
Reaction #156350
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1ccc2ncc(-c3ccc4ccccc4n3)n2n1
Reaction #156351
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(c1cc2cn[nH]c2cc1F)c1cnc2ccc(-c3cnn(C)c3)nn12
Reaction #156387
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1cc(-c2ccc3ncc(Cc4cc5cn[nH]c5cc4F)n3n2)cn1
Reaction #156388
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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