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C1CCC(NC2CCCCC2)CC1

C1CCC([NH2+]C2CCCCC2)CC1.O=C([O-])c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-]
Reaction #55600
product
収率 59.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCC(=O)N(c1ccc(N(C2CCCCC2)C2CCCCC2)cc1)C1CCCCC1
Reaction #68739
N,N,N′-tricyclohexyl-N′-methoxypropionyl-para-phenylenediamine
DOI: 10.6084/m9.figshare.5104873.v1
C1CCC([NH2+]C2CCCCC2)CC1.O=C([O-])c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-]
Reaction #93612
product
収率 59.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCSc1cnc(NC(=O)N(C2CCCCC2)C2CCCCC2)s1
Reaction #173899
DOI: 10.1039/C8SC04228D
O=C(O)C(=NO)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #173993
DOI: 10.1039/C8SC04228D
COC(=O)CCSc1cnc(NC(=O)N(C2CCCCC2)C2CCCCC2)s1
Reaction #179382
DOI: 10.1039/C8SC04228D
c1cc2[nH]ncc2cc1NC1CCC(NC2CCCCC2)CC1
Reaction #182690
DOI: 10.1039/C8SC04228D
O=C(OCc1ccccc1)C1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)C1
Reaction #182826
DOI: 10.1039/C8SC04228D
CN(C)C1(c2ccccc2)CCC(=CC(=O)N2CCC(c3c[nH]c4ccccc34)C2)CC1
Reaction #187453
DOI: 10.1039/C8SC04228D
Cc1nc(NC(=O)N(C2CCCCC2)C2CCCCC2)sc1SCCN1CCCCC1
Reaction #191937
DOI: 10.1039/C8SC04228D
O=C(c1csc(NC(=O)N(C2CCCCC2)C2CCCCC2)n1)N1CCOCC1
Reaction #206977
DOI: 10.1039/C8SC04228D
C1CCC(NC2CCCCC2)CC1
Reaction #214761
dicyclohexylamine
収率 74.7%DOI: 10.6084/m9.figshare.5104873.v1
C1CCC(NC2CCCCC2)CC1
Reaction #214764
dicyclohexylamine
収率 82.7%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccnc1Sc1cnc(NC(=O)N(C2CCCCC2)C2CCCCC2)s1
Reaction #222199
DOI: 10.1039/C8SC04228D
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCC(C)CC3)s2)CC1
Reaction #224836
DOI: 10.1039/C8SC04228D
O=C(Nc1ncc(Sc2ccccn2)s1)N(C1CCCCC1)C1CCCCC1
Reaction #232917
DOI: 10.1039/C8SC04228D
N=C(c1ccccc1)N(C1CCCCC1)C1CCCCC1
Reaction #238482
DOI: 10.1039/C8SC04228D
COC(=O)CSc1cnc(NC(=O)N(C2CCCCC2)C2CCC(C(F)(F)F)CC2)s1
Reaction #241323
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCC(=O)N1CC2(CCCCC2)NC2(CCCCC2)C1
Reaction #242595
DOI: 10.1039/C8SC04228D
CC1CCC(N(C(=O)Nc2ncc(SCCCN3CCOCC3)s2)C2CCCCC2)CC1
Reaction #242778
DOI: 10.1039/C8SC04228D
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