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1424623

CCOP(=O)(OCC)C(CC(=O)O)P(=O)(OCC)OCC
Reaction #2064
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1CP(=O)(OC(C)C)OC(C)C
Reaction #5007
diisopropyl 2-methylbenzylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(Cc1ccc(Br)cc1C)OCC
Reaction #5011
Diethyl 2-methyl-4-bromobenzylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(Cc1ccccc1C(=O)O)OCC
Reaction #5012
Diethyl 2-carboxybenzylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OP(=O)(OCCl)OC(C)(C)C
Reaction #48488
di-tert-butyl chloromethyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OP(=O)(OCCl)OC(C)(C)C
Reaction #48489
di-tert-butyl chloromethyl phosphate
Ausbeute 343.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OP(=O)(OCCl)OC(C)(C)C
Reaction #48490
di-tert-butyl chloromethyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCNC(=O)OC(C)(C)C)OP(=O)(O)C(NC(=O)C(Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C
Reaction #58023
2-{[1-(2-benzyloxycarbonylamino-3-phenyl-propionylamino)-2-methyl-propyl]-hydroxy-phosphinoyloxy}-5-tert-butoxycarbonylamino-pentanoic acid methyl ester
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)C(Cc1ccccc1)NC(=O)OCc1ccccc1)P(=O)(O)OC(CCCNC(=O)OC(C)(C)C)C(=O)O
Reaction #58024
2-{[1-(2-benzyloxycarbonylamino-3-phenyl-propionylamino)-2-methyl-propyl]-hydroxy-phosphinoyloxy}-5-tert-butoxycarbonylamino-pentanoic acid
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(Cc1ccccc1CN1C(=O)c2ccccc2C1=O)OCC
Reaction #58962
diethyl {2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]benzyl}phosphonate
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COCc1ccccc1C(C(=O)O)P(=O)(OC)OC
Reaction #64885
dimethylphosphono-(2-methoxymethylphenyl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(-c3cccc(F)c3)cc(=O)c2c1OP(=O)(O)O
Reaction #66913
52
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OP(=O)(OCc2ccccc2)OCc2ccccc2)cc(C2=Nc3cc4c(cc3C(=O)C2)OCO4)c1
Reaction #66939
168
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CP(=O)(OCC)c1ccc(O)c(C(C)(C)CC(=O)OCc2ccccc2)c1)OCC
Reaction #67555
122
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CP(=O)(OCC)c1ccc(OC(=O)CC)c(C(C)(C)CC(=O)OCc2ccccc2)c1)OCC
Reaction #67556
123
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CP(=O)(OCC)c1ccc(OC(=O)CC)c(C(C)(C)CC(=O)O)c1)OCC
Reaction #67557
liquid 124
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #67558
liquid
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CP(=O)(OCC)c1ccc(OC(=O)CC)c(C(C)(C)CC(=O)N[C@@H](Cc2ccccc2)C(=O)O)c1)OCC
Reaction #67559
liquid 126
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1-c1cc(Cl)ccc1Oc1ccc(S(=O)(=O)/N=c2\sccn2COP(=O)(OC(C)(C)C)OC(C)(C)C)cc1C#N
Reaction #74554
title compound
Ausbeute 84.9%DOI: 10.6084/m9.figshare.5104873.v1
O=P(O)(O)C(c1ccc2cc(O)ccc2c1)P(O)(O)=S
Reaction #81387
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
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