部分構造検索

16759924

C=Cc1ccc(OCCC2OCCCO2)cc1
Reaction #880
2-[2-(4-vinylphenoxy)ethyl]-[1,3]-dioxane
収率 77.6%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(OCCC2OCCO2)cc1
Reaction #882
2-[2-(4-vinylphenoxy)ethyl]-[1,3]-dioxolan
収率 88.5%DOI: 10.6084/m9.figshare.5104873.v1
C(=C\c1ccccn1)/CC1OCCCO1
Reaction #981
E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCCCCCCCOC1CCCCO1
Reaction #1208
1-(2-tetrahydropyranyloxy)-15-hexadecene
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(C)c(I)c1
Reaction #3070
3-iodo-4-methylstyrene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCc1cc2ccccc2o1
Reaction #3157
2-octylbenzofuran
収率 76.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCOc1ccc(OCCCO)cc1
Reaction #3777
ethyl 5-[4-(3-hydroxypropyloxy)phenoxy]pentanoate
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #3860
yellow oil
DOI: 10.6084/m9.figshare.5104873.v1
C=C(c1ccc(C#N)cc1)c1cncs1
Reaction #6030
1-(4-Cyanophenyl)-1-(5-thiazolyl)-ethylene
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)C(F)(F)F.[Br-]
Reaction #6300
4-Triflylbenzyltriphenylphosphonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCCO)C(=CC=Cc1ccccc1)c1ccc(S(=O)(=O)C(F)(F)F)cc1
Reaction #6301
compound C
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nc3ccccc3o2)cc1[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #6307
4-(Benzoxazol-2-yl)tolyltriphenylphosphonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
OCCCCCCN1CCCc2cc(C=CC=Cc3ccc(-c4nc5ccccc5o4)cc3)ccc21
Reaction #6308
1-(N-hydroxyhexyl-1,2,3,4-tetrahydroquinolin-6-yl)-4-(4-benzoxazol-ylphenyl)-1,3-butadiene
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(O)c(Cl)c1
Reaction #7390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCC2(CCCC)Cc3cc(O)ccc3C2=C1Br
Reaction #7929
4-bromo-9a-butyl-3-methylene-2,3,9,9a-tetrahydro-1H-fluoren-7-ol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(C(F)(F)F)cc2)oc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #9745
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CCc2oc(-c3ccc(C(F)(F)F)cc3)cc2CO)cc1
Reaction #9746
{2-[2-(4-methylphenyl)ethyl]-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCc1oc(-c2ccc(C(F)(F)F)cc2)cc1CO
Reaction #9747
{2-isopentyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1oc(-c2ccc(C(F)(F)F)cc2)cc1CO
Reaction #9748
{2-isobutyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@@H](C(=O)OC)N(C(=O)OCc2ccccc2)C1
Reaction #9987
title compound
収率 72.6%DOI: 10.6084/m9.figshare.5104873.v1
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