部分構造検索

343231

Cc1ccc2c(N3CCNCC3)c(F)ccc2n1
Reaction #44107
title compound
収率 156.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCNC(=O)C1(c2ccc(C)cc2)CC1
Reaction #76082
1-p-tolyl-cyclopropanecarboxylic acid heptylamide
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCNCC1(c2ccc(CO)cc2)CC1
Reaction #76083
[4-(1-heptylaminomethyl-cyclopropyl)-phenyl]-methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)CN1CCC(c2noc3cc(F)ccc23)CC1.O=C(O)/C=C/C(=O)O
Reaction #83928
expected product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC2(CC1)CNc1ccccc12
Reaction #156267
title compound
収率 34.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CC2(CC2)CC1c1nc2ccc(Br)cc2[nH]1
Reaction #159127
6-(6-Bromo-1H-benzoimidazol-2-yl)-5-aza-spiro[2.4]heptane-5-carboxylic acid benzyl ester
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1nc2ccc(Br)cc2[nH]1)C(C)C
Reaction #159128
{1-[6-(6-Bromo-1H-benzoimidazol-2-yl)-5-aza-spiro[2.4]heptane-5-carbonyl]-2-methyl-propyl}-carbamic acid methyl ester
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](c2ccccc2)CN1CC12CC3CC(CC(C3)C1)C2
Reaction #162326
(S)-3-((1-adamantyl)methyl)-5-phenyloxazolidin-2-one
収率 64.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](C2CCCCC2)CN1CC12CC3CC(CC(C3)C1)C2
Reaction #162333
(S)-3-((1-adamantyl)methyl)-5-cyclohexyloxazolidin-2-one
収率 50.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1CCN(CC23CC4CC(CC(C4)C2)C3)C(=O)O1
Reaction #162338
3-((1-adamantyl)methyl)-6-isobutyl-1,3-oxazinan-2-one
収率 218.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(CC23CC4CC(CC(C4)C2)C3)C(=O)O1
Reaction #162348
3-((1-adamantyl)methyl)-6-methyl-1,3-oxazinan-2-one
収率 54.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CC2(CC2)CC1c1nc2ccc(Br)cc2[nH]1
Reaction #167074
6-(6-Bromo-1H-benzoimidazol-2-yl)-5-aza-spiro[2.4]heptane-5-carboxylic acid benzyl ester
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC2(C(=O)O)CN(C(=O)OCc3ccccc3)CC12
Reaction #176959
DOI: 10.1039/C8SC04228D
COc1cc(Cl)ccc1NC(=O)C1(C)CCCn2c1nc(-c1ccncn1)cc2=O
Reaction #180424
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CNc1cc(Cl)cnc12
Reaction #187733
DOI: 10.1039/C8SC04228D
C=C(C)C1(CC(C)C)CCN(CC(=O)OCC)C1=O
Reaction #193350
DOI: 10.1039/C8SC04228D
COc1cc(NC(=O)C(C)(C)C)ccc1C(=O)N(C)C
Reaction #196417
DOI: 10.1039/C8SC04228D
CCC1(CCCBr)C(=O)NC(=O)NC1=O
Reaction #204317
DOI: 10.1039/C8SC04228D
Cl
Reaction #204547
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C#N)(C(=O)N2CCOCC2)CC1
Reaction #211457
DOI: 10.1039/C8SC04228D
1 ページ次のページ