部分構造検索

9832

CCOC(=O)C1=C(CSCCN)NC(C)=C(C(=O)OC)C1c1cccc([N+](=O)[O-])c1.O=C(O)/C=C/C(=O)O
Reaction #5745
(-)-2-(aminoethylthio)methyl-3-carboethoxy-5-carbomethoxy-4-(3-nitrophenyl)-6-methyl-1,4-dihydropyridine fumarate
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)CSSCC(F)(F)F
Reaction #343944
bis-(2,2,2-trifluoroethyl) disulphide
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)CSCc1ccccc1
Reaction #343945
2,2,2-trifluoroethylthiomethylbenzene
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CC1(c2cccnc2)CCN(Cc2ccccc2)CC1
Reaction #430713
1-benzyl-4-(pyrid-3-yl)-4-cyanopiperidine hydrochloric acid salt
DOI: 10.6084/m9.figshare.5104873.v1
FCc1cccc(Oc2ccccc2)c1
Reaction #441880
3-phenoxybenzyl fluoride
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #453648
3-Amino-1-benzhydrylazetidine
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CC1(c2ccncc2)CCN(Cc2ccccc2)CC1
Reaction #487243
1-benzyl-4-cyano-4-(pyridin-4-yl)-piperidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(c2ccccn2)CCN(Cc2ccccc2)CC1
Reaction #487249
1-benzyl-4-cyano-4-(pyridin-2-yl)-piperidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)CCC[CH2][Sn]([CH3])([CH3])[CH3])cc1
Reaction #530544
4-(p-tolylsulfonyl)butyltrimethylstannane
収率 37.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1cccnc1Oc1cccc(O)c1
Reaction #554228
methyl 2-(3-hydroxyphenoxy)-3-pyridinylacetate
収率 51.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1c(C)n(Cc2ccc([N+](=O)[O-])cc2)c2ccccc12
Reaction #676514
product
収率 3.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NS(=O)(=O)c1sc(Cl)cc1N
Reaction #688479
title compound
収率 39.5%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #707008
EtOAc hexanes
収率 5.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #708105
1-benzhydryl-3-phthalimidoazetidine
収率 67.4%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)OCCCCO[Si](C)(C)C
Reaction #934669
1,4-bis-trimethylsiloxybutane
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCCCCOCC(F)(F)c1ccccc1
Reaction #972707
title compound
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
FCc1cccc(Oc2ccccc2)c1
Reaction #981517
3-phenoxybenzyl fluoride
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)CCC[CH2][Sn]([CH3])([CH3])[CH3])cc1
Reaction #1058882
4-(-p-tolylsulfonyl)butyltrimethylstannane
収率 37.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Cl)cc(C(C)(C)N)cc1Cl
Reaction #1171812
desired compound
収率 63.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1cccnc1Oc1cccc(O)c1
Reaction #1172280
methyl 2-(3-hydroxyphenoxy)-3-pyridinylacetate
収率 51.5%DOI: 10.6084/m9.figshare.5104873.v1
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