部分構造検索

13901

CC(C)(C)OC(=O)N[C@@H](CC1CCCC1)[C@H](O)CO
Reaction #42553
tert-butyl (1S,2S)-1-[cyclopentylmethy]-2,3-dihydroxypropylcarbamate
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)CC1
Reaction #57277
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc3c2cc(C2(O)CCN(C(=O)OC(C)(C)C)CC2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #57278
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCOc2ccc(C=O)cc21
Reaction #60349
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCOc2ccc(CN3CCCCC3)cc21
Reaction #60350
(6-piperidin-1-ylmethyl-chroman-4-yl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1CCOc2cc(C#N)ccc21
Reaction #60396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)c1cc(-c3ccc(C(N)=O)cn3)ccc1O2
Reaction #66756
compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC(=O)c1ccc(-c2ccc3c(c2)C(=O)CC2(CCNCC2)O3)nc1
Reaction #66757
6-(4-Oxospiro[chroman-2,4′-piperidin]-6-yl)nicotinamide dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CN(Cc2ccccc2)CC2(CCN(C(=O)OC(C)(C)C)CC2)O1
Reaction #160054
9-tert-butyl 2-methyl 4-benzyl-1-oxa-4,9-diazaspiro[5.5]undecane-2,9-dicarboxylate
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CNCC2(CCN(C(=O)OC(C)(C)C)CC2)O1
Reaction #160055
9-tert-butyl 2-methyl 1-oxa-4,9-diazaspiro[5.5]undecane-2,9-dicarboxylate
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccccc2-c2nc3c(C(=O)Nc4nccs4)cccc3[nH]2)C1
Reaction #172299
title compound 32
収率 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C(Cc2cc(F)cc(F)c2)C(C2CC(O)(c3ccccc3)CN2C(=O)OC(C)(C)C)OC1(C)C
Reaction #174132
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)c1cc(-c3noc(=O)[nH]3)ccc1O2
Reaction #177360
DOI: 10.1039/C8SC04228D
COc1ccc(COC2CC(C3OC(C)(C)N(C(C)=O)C3Cc3cc(F)cc(F)c3)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #177824
DOI: 10.1039/C8SC04228D
C=CCOc1cc(OC2CCN(C(=O)OC(C)(C)C)CC2)ccc1C(=O)O
Reaction #178517
DOI: 10.1039/C8SC04228D
COCC1CC(c2ncc(-c3ccc4c(c3)COc3cc5c(ccc6nc(C7CCC(C)N7)[nH]c65)cc3-4)[nH]2)N(C(=O)OC(C)(C)C)C1
Reaction #178783
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2ccc(CC(NC(=O)C3(NC(=O)OC(C)(C)C)CCOCC3)C(N)=O)cc2)cc1C#N
Reaction #180142
DOI: 10.1039/C8SC04228D
CCn1cc(-c2cnc3c(c2)c(-c2cncc(OC4CCN(C(=O)OC(C)(C)C)CC4)n2)cn3S(=O)(=O)c2ccccc2)cn1
Reaction #180944
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC(C(=O)O)N(C(=O)OC(C)(C)C)C3)cc(-c3nc(C(F)(F)F)cs3)nc2c1C
Reaction #183244
DOI: 10.1039/C8SC04228D
CN1C(=O)Cc2ccc(-c3ccc(CC(NC(=O)C4(NC(=O)OC(C)(C)C)CCOCC4)C(N)=O)cc3)cc21
Reaction #197080
DOI: 10.1039/C8SC04228D
1 ページ次のページ