部分構造検索

O=C(Cl)OCCl

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1502
3-(Chloromethoxycarbonyl) Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)OC(=O)OC(C)(C)C
Reaction #4521
α-chloroethyl tert-butyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)OC(=O)Oc1cccc2c1OC(C)(C)C2
Reaction #4524
1-chloroethyl 2,3-dihydro-2,2-dimethyl-7-benzofuranyl carbonate
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)OC(Cl)C(Cl)(Cl)Cl
Reaction #4526
1,2,2,2-tetrachloroethyl N-methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2c(ccc3c2CCNC3)C1=O
Reaction #5034
6,7,8,9-tetrahydro-1H-pyrrolo[2,3-f]isoquinoline-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(F)c(I)cc2c(=O)o1
Reaction #6918
title compound
収率 90.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N2CCCC(C2)N1Cc1ccccc1
Reaction #43768
expected product
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCC(Cl)=C1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC1.O=C(O)C(F)(F)F
Reaction #43783
72
収率 27.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)ccc3Oc3ccccc3[C@H]12)OCCl
Reaction #44437
trans-(7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)carbamic acid chloromethyl ester
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Nc2ncnc3c2CNCC3)cc1)C(F)(F)F
Reaction #47911
product
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CO/N=C(\C(=O)Cl)c1nsc(N)n1
Reaction #50754
2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)CN1CCNCC1)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1.Cl.Cl
Reaction #53056
(Z)-3-{1-[4-(N-piperazinomethylcarbonyl-N-methyl-amino)-phenylamino]-1-phenyl-methylidene}-2-indolinone-dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)CN1CCNCC1)c1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1.Cl.Cl
Reaction #53098
(Z)-3-{1-[4-(N-piperazinomethylcarbonyl-N-methyl-amino)phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone-dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(F)c(F)c1)[C@H]1CC[C@H](O)CC1
Reaction #53820
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 3,4-difluoro-phenyl ester
収率 238.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(F)cc1F)[C@H]1CC[C@H](OCCCCBr)CC1
Reaction #53831
trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 2,4-difluoro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C(=O)C2CCNCC2)n1)c1c(F)cc(F)cc1F
Reaction #58497
title compound
収率 29.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #58515
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
Brc1sc2c(c1Br)CC1CNCC21
Reaction #58529
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2c1C(C)C1CNCC21
Reaction #58537
6,7-Dimethyl-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[α]pentalene
DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c(s1)CC1CCNCC21
Reaction #58551
subtitle compound
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ