部分構造検索

610184

CC(=O)C(C(=O)c1ccccc1)=C1CCCCN1
Reaction #94446
1-phenyl-2-(2-piperidinylidene)-1,3-butanedione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(C(=O)c1ccccc1)=C1CCCCN1
Reaction #197905
DOI: 10.1039/C8SC04228D
C=CCC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CSCC)C1=O
Reaction #228988
DOI: 10.1039/C8SC04228D
C=CCC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CSCC)C2CC2)C1=O
Reaction #273767
DOI: 10.1039/C8SC04228D
CC1CCNC(=C2C(=O)CC(C)(C)CC2=O)C1
Reaction #572787
pure material
収率 17.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(CC)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CSCC)C2CC2)C1=O
Reaction #756967
DOI: 10.1039/C8SC04228D
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)[N+]2=C1O[C@@H](C)[C@@H]2CC.O=S(=O)([O-])C(F)(F)F
Reaction #1019288
(2S,3S,5S,6R,8S)-8-allyl-6-(3-chlorophenyl)-5-(4-chlorophenyl)-3-ethyl-2,8-dimethyl-2,3,5,6,7,8-hexahydrooxazolo[3,2-a]pyridin-4-ium triflate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@@H](CC)CSCC)C1=O
Reaction #1019418
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@@H](CC)CS(=O)(=O)C2CC2)C1=O
Reaction #1019419
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(CC)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)[N+]2=C1OC[C@@H]2CC.CS(=O)(=O)[O-]
Reaction #1019420
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@H](CSCC)C2CC2)C1=O
Reaction #1019421
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(CC)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@H](CSCC)C2CC2)C1=O
Reaction #1019422
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)[N+]2=C1OC[C@@H]2C(C)(C)C.O=S(=O)([O-])C(F)(F)F
Reaction #1019424
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@H](CO)C(C)(C)C)C1=O
Reaction #1019425
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@H](CS)C2CC2)C1=O
Reaction #1019426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)[N+]2=C1OC(C)[C@@H]2CC.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #1019428
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cc(F)cc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@@H](CC)CS(C)(=O)=O)C1=O
Reaction #1019440
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)[N+]2=C1O[C@@H](C)[C@@H]2CC.O=S(=O)([O-])C(F)(F)F
Reaction #1135602
(2S,3S,5S,6R,8S)-8-allyl-6-(3-chlorophenyl)-5-(4-chlorophenyl)-3-ethyl-2,8-dimethyl-2,3,5,6,7,8-hexahydrooxazolo[3,2-a]pyridin-4-ium triflate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@@H](CC)CSCC)C1=O
Reaction #1135732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@]1(C)C[C@H](c2cccc(Cl)c2)[C@@H](c2ccc(Cl)cc2)N([C@@H](CC)CS(=O)(=O)C2CC2)C1=O
Reaction #1135733
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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