子结构搜索

4395

O=C(c1ccc(NP(=O)(c2ccccc2)c2ccccc2)cc1)N1Cc2cccn2Cc2ccccc21
Reaction #3678
white solid
收率 96.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(N)=O)[N+](C)(C)C3)[C@H](C)[C@H]12
Reaction #5154
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3CC[N+](C)(C)C3)C[C@H]12
Reaction #5155
title compound
收率 18.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(N)=O)[N+](C)(C)C3)C[C@H]12
Reaction #5158
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cccn2cn1
Reaction #53434
product
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(=O)NC(C)(C)C[NH+]4CCCC4)C3)[C@H](C)[C@H]12.O=S(=O)([O-])F
Reaction #65613
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(NP(=O)(c2ccccc2)c2ccccc2)cc1)N1Cc2cccn2Cc2ccccc21
Reaction #83499
white solid
收率 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](/C=C/CCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)NP(=O)(c1ccccc1)c1ccccc1
Reaction #157668
crude title compound
收率 119.6%DOI: 10.6084/m9.figshare.5104873.v1
NOP(=O)(c1ccccc1)c1ccccc1
Reaction #160830
above compound
收率 82.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC1NC(C(=O)Nc2ccc(C#N)cc2F)C(c2cccc(Cl)c2F)C12C(=O)Nc1cc(Cl)ccc12
Reaction #181267
DOI: 10.1039/C8SC04228D
COc1cc(OCCCS(C)(=O)=O)ccc1NC(=O)C1NC(CC(C)(C)C)C2(C(=O)Nc3cc(Cl)ccc32)C1c1cccc(Cl)c1F
Reaction #188072
DOI: 10.1039/C8SC04228D
CC(=O)c1ccc(NC(=O)C2NC(CC(C)(C)C)C3(C(=O)Nc4cc(Cl)ccc43)C2c2cccc(Cl)c2F)cc1
Reaction #208577
DOI: 10.1039/C8SC04228D
NC(=O)c1ccc(NP(=O)(c2ccccc2)c2ccccc2)nc1
Reaction #215126
6-diphenylphosphorylamino nicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCOCC2)ccc1NC(=O)C1NC(CC(C)(C)C)C2(C(=O)Nc3cc(Cl)ccc32)C1c1cccc(Cl)c1F
Reaction #221467
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1NC(C(=O)Nc2ccc(C#N)cc2)C(c2cccc(Br)c2F)C12C(=O)Nc1cc(Cl)ccc12
Reaction #223335
DOI: 10.1039/C8SC04228D
COCCOCOc1c(OC)cc(C=CC=CC(=O)NCCN2CCC(c3c[nH]c4ccccc34)CC2)cc1OC
Reaction #225040
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)C(Cc1ccc(OC(C)(C)C)cc1)N(C)C(=O)OC(C)(C)C)C(=O)NCCCc1ccccc1
Reaction #231776
DOI: 10.1039/C8SC04228D
CC(C)CC(C=CCCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)NP(=O)(c1ccccc1)c1ccccc1
Reaction #232559
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(F)c(NC(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)cc1F
Reaction #233823
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1NC(C(=O)Nc2ccc(C#N)cc2)C(c2cccc(Cl)c2F)C12C(=O)Nc1cc(Cl)ccc12
Reaction #247731
DOI: 10.1039/C8SC04228D
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