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CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccccc1[N+](=O)[O-]
Reaction #6142
expected product
収率 15.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1O[C@@H]1SC[C@@H](O)[C@H](O)[C@H]1O
Reaction #6143
expected product
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(OCC2CC2)c(Cl)cc2c1[nH]c1cnccc12
Reaction #40472
6-chloro-7-cyclopropylmethyoxy-8-nitro-9H-β-carboline
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(OCC2CC2)c(Cl)cc2c1[nH]c1cnccc12
Reaction #40473
6-chloro-7-cyclopropylmethoxy-9H-β-carbolin-8-ylamine
収率 80.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2cc(F)c3c(c2)OCC2CCCN32)c(C)n1
Reaction #84386
title compound
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCOc2c(Nc3ncc(Cl)c(Nc4ccccc4OCC#N)n3)cccc21
Reaction #174626
DOI: 10.1039/C8SC04228D
CCCCCCC(C)Oc1ccc(-c2ccc(C(=O)OC)cc2)cc1N
Reaction #178615
DOI: 10.1039/C8SC04228D
CCOP(=O)(CC(=O)Nc1cc2c(Nc3ccc(F)c(Cl)c3)ncnc2cc1OCC1CC1)OCC
Reaction #180200
DOI: 10.1039/C8SC04228D
Nc1cc(F)cc2c1OCCC21SC(=O)NC1=O
Reaction #198339
DOI: 10.1039/C8SC04228D
CCn1cc(CN(C(=O)C2CCOc3c(N)cccc32)c2ccc(C(C)C)cc2)cn1
Reaction #204035
DOI: 10.1039/C8SC04228D
CCOC(=O)C=CC(=O)Nc1cc2c(Nc3ccc(F)c(Cl)c3)ncnc2cc1OCC1CC1
Reaction #207530
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccccc1OC1CCCC1
Reaction #219032
2-(Cyclopentyloxy)-1-nitrobenzene
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1OCC1CCCC1
Reaction #219035
2-(Cyclopentylmethoxy)-1-nitrobenzene
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1cc(C)ccc1[N+](=O)[O-]
Reaction #219128
3-(1-Butoxy)-4-nitrotoluene
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)Nc2nccs2)c(OC2CCCC2)c1
Reaction #219134
1-(2-Cyclopentyloxy-4-methyl-phenyl)-3-thiazol-2-yl-urea
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([N+](=O)[O-])c(OCC2CCCC2)c1
Reaction #219138
3-Cyclopentylmethoxy-4-nitrotoluene
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)Nc2nc(CC(=O)O)cs2)c(OC2CCCC2)c1
Reaction #219139
{2-[3-(2-Cyclopentyloxy-4-methyl-phenyl)-ureido]-thiazol-4-yl}-acetic acid
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1ccc(-n2cc(C(=O)NC3CC3)nn2)c(OCCCCCCF)c1
Reaction #223508
DOI: 10.1039/C8SC04228D
CCOC(=O)COc1cc(OC)c2c(c1[N+](=O)[O-])OC1(CCCCC1)CC2=O
Reaction #225949
DOI: 10.1039/C8SC04228D
CCNC(=O)c1cccc(F)c1Nc1nc(Nc2cccc3c2OCCCC3(C)C)ncc1Cl
Reaction #227220
DOI: 10.1039/C8SC04228D
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