部分構造検索

742367

CCOP(C)(=O)CCN(C(=O)C1CCC(C)CC1)c1cc(C#CC(C)(C)C)sc1C(=O)OC
Reaction #178280
DOI: 10.1039/C8SC04228D
O=C(O)C1CC(C2CCCCC2)CN1C(=O)CP(=O)(O)CCCCc1ccccc1
Reaction #190894
DOI: 10.1039/C8SC04228D
CCOP(=O)(CCCCc1ccccc1)CC(=O)N1CC2(CC1C(=O)O)SCCS2
Reaction #193878
DOI: 10.1039/C8SC04228D
CCOP(=O)(CC(=O)N1CCCC1C(=O)O)C(CCc1ccccc1)CC(=O)c1ccccc1
Reaction #274518
DOI: 10.1039/C8SC04228D
O=C(O)C1Cc2ccccc2CN1C(=O)CP(=O)(O)CCCCc1ccccc1
Reaction #298647
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCOP(=O)(CC(=O)Nc1c(C(C)C)cccc1C(C)C)c1ccccc1
Reaction #335006
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NC(CCc1ccccc1)P(=O)(O)CC(=O)N1CCCC1C(=O)O
Reaction #373091
DOI: 10.1039/C8SC04228D
CCC(=O)OC(OP(=O)(CCCCc1ccccc1)CC(=O)N1CC2(C[C@H]1C(=O)O)SCCS2)C1CCCCC1
Reaction #445712
syrup
収率 158.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(C)(=O)C(C(=O)NC=Cc1ccc(F)c(F)c1)c1csc2ccc(Cl)cc12
Reaction #476513
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(C)(=O)C(C(=O)NC=Cc1ccc(F)c(F)c1)c1csc2ccc(Cl)cc12
Reaction #476514
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CP(=O)(O)C(C(=O)NC=Cc1ccc(F)c(F)c1)c1csc2ccc(Cl)cc12
Reaction #476515
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(C)(=O)C(C(=O)NC=Cc1ccc(F)c(F)c1)c1csc2ccc(Cl)cc12
Reaction #476518
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCc1ccccc1)CC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)OC
Reaction #521591
N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl ester
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCc1ccccc1)CC(=O)N1CCC[C@H]1C(=O)O
Reaction #833251
title compound
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CP(=O)(O)C(C(=O)NC=Cc1ccc(F)c(F)c1)c1csc2ccc(Cl)cc12
Reaction #920502
DOI: 10.1039/C8SC04228D
COC(=O)[C@@H]1CC2(CN1C(=O)CP(=O)(O)CCCCc1ccccc1)SCCS2
Reaction #938608
title compound
収率 92.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCc1ccccc1)CC(=O)N1CC(O)C[C@H]1C(=O)OC
Reaction #938610
title compound
収率 90.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCc1ccccc1)CC(=O)N1CC(N=[N+]=[N-])C[C@H]1C(=O)OC
Reaction #938611
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CC(N=[N+]=[N-])CN1C(=O)CP(=O)(O)CCCCc1ccccc1
Reaction #938612
title compound
収率 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OCOC(=O)[C@@H]1CC2(CN1C(=O)CP(=O)(O)CCCCc1ccccc1)SCCS2
Reaction #938616
(S)-7-[[Hydroxy(4-phenylbutyl)phosphinyl]acetyl]-1,4-dithia-7-azaspiro[4.4]nonane-8-carboxylic acid, (2,2-dimethyl-1-oxopropoxy)methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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