子结构搜索

19205

C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #1579
title product
收率 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #1580
title product
收率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=CCCC(CCOCc2ccccc2)C1
Reaction #9391
5-(2-benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCCC(CCOCc2ccccc2)C1
Reaction #9392
[2-(3-methyl-cyclohex-3-enyl)-ethoxymethyl]-benzene
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C2CCCCC12
Reaction #10583
1,2,3,4,4a,5,6,7,8,9a-decahydro-9H-fluoren-9-one
收率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)C2=C(CCCC2)C1=O)C1(C)OCCO1
Reaction #10959
Ethyl 3-(1,3-dioxo-1,3,4,5,6,7-hexahydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1
Reaction #43884
oseltamivir
收率 108.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=C(O)C(O)C(O)C(=O)O
Reaction #43885
oseltamivir tartrate
收率 97.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=P(O)(O)O
Reaction #43886
oseltamivir phosphate
收率 56.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49741
N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC1Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #49744
N-{2-fluoro-4-chloro-5-(2-methylcyclopentyl)oxyphenyl}-3,4,5,6-tetrahydrophthalimide
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCCC2)c(Cl)cc1F
Reaction #49745
N-(2-fluoro-4-chloro-5-cyclohexyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #49756
N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50001
N-(2,4-Dichloro-6-fluorobenzothiazol-7-yl)-3,4,5,6-tetrahydrophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=CCCC(CCOCc2ccccc2)C1
Reaction #57032
5-(2-benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCCC(CCOCc2ccccc2)C1
Reaction #57033
[2-(3-methyl-cyclohex-3-enyl)-ethoxymethyl]-benzene
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH][nH]c(=O)c2c1CCCC2
Reaction #70498
2,3,5,6,7,8-hexahydro-phthalazin-1,4-dione
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)C1=C1C=CNC=C1
Reaction #78167
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #80706
title product
收率 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #80707
title product
收率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
第 1 页下一页