部分構造検索

COC1CCNCC1

COc1cccc(OC2CCN(c3ccc4nnc(C(F)(F)F)n4c3)CC2)c1
Reaction #227
収率 30.5%
COc1cncc(N2CCC3(CC2)OCCO3)c1
Reaction #550
収率 75.1%
COC(=O)COc1ccc(OC2CCN(c3ccncc3)CC2)cc1
Reaction #2322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(Oc2cccc3ncc([N+](=O)[O-])n23)CC1
Reaction #5571
desired product
収率 54.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(Oc2cccc3ncc(N)n23)CC1
Reaction #5572
desired product
収率 132.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1C2CC(O)CC1C1OC12
Reaction #42721
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(OC(=O)C(Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C(=O)OC2CC(C)(C)NC(C)(C)C2)CC(C)(C)N1
Reaction #55627
3,5-di-tert.butyl-4-hydroxybenzyl-malonic acid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](F)COC1CCNCC1
Reaction #156308
4-{[(2S)-2-fluoropropyl]oxy}piperidine
収率 43.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2CCC3(CC2)CNCC(c2ccccc2)O3)ccc1OC(C)C
Reaction #160193
(4-isopropoxy-3-methyl-phenyl)-(8-phenyl-7-oxa-3,10-diazaspiro[5.5]undecan-3-yl)methanone
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2CCC3(CC2)CN(C)CC(c2ccccc2)O3)ccc1OC(C)C.Cl
Reaction #160194
(4-isopropoxy-3-methyl-phenyl)-(10-methyl-8-phenyl-7-oxa-3,10-diazaspiro[5.5]undecan-3-yl)methanone hydrochloride salt
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2CCC3(CC2)CN(C(C)C)CC(c2ccccc2)O3)ccc1OC(C)C.Cl
Reaction #160195
(4-isopropoxy-3-methyl-phenyl)-(10-isopropyl-8-phenyl-7-oxa-3,10-diazaspiro[5.5]undecan-3-yl)methanone hydrochloride salt
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CCNC[C@H]1C
Reaction #167933
(3R,4R)-4-Methoxy-3-methylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CCC(OCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(c2ccccc2)C1
Reaction #173596
DOI: 10.1039/C8SC04228D
O=C(Nc1ccccc1-c1ccccc1)OC1CCN(CCNCC(=O)c2cccc(C(=O)NCCNCc3ccc(O)cc3)c2)CC1
Reaction #175025
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCC(Oc2ccccc2[N+](=O)[O-])CC1)c1cc(-c2ccccc2)[nH]n1
Reaction #175849
DOI: 10.1039/C8SC04228D
CNC(=O)N1CCC(Oc2ccc(C(F)(F)F)cc2)(c2ccccc2)CC1
Reaction #180734
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)N1CCC(OCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(c2ccccc2)C1
Reaction #181108
DOI: 10.1039/C8SC04228D
CC(C)=CCCN1CCC(OC(=O)C(O)(c2ccccc2)C2CCC2)CC1
Reaction #182398
DOI: 10.1039/C8SC04228D
CCOC(=O)CNC(=O)N1CCC(OCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(c2ccccc2)C1
Reaction #183420
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)NC2CC2)cc1NC(=O)c1cc(OC2CCN(C3CC3)CC2)ccc1[N+](=O)[O-]
Reaction #186140
DOI: 10.1039/C8SC04228D
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