بحث البنية الفرعية

356462

C#CCC1C(=O)N(C)OC1c1ccccc1
Reaction #907
2-methyl-5-phenyl-4-propargylisoxazolin-3-one
المردود 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(CC(=O)O)c1ccc(OCN2C(=O)C(C)(C)c3cc(C(F)(F)F)ccc32)cc1
Reaction #68763
3-[4-(3,3-dimethyl-2-oxo-5-trifluoromethyl-2,3-dihydroindol-1-ylmethoxy)phenyl]hex-4-ynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(CC(=O)O)c1ccc(OCn2c(=O)sc3ccccc32)cc1
Reaction #68766
3-[4-(2-oxobenzothiazol-3-ylmethoxy)-phenyl]hex-4-ynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(CC(=O)O)c1ccc(OCN2C(=O)C(C)(C)Oc3ccccc32)cc1
Reaction #68767
3-[4-(2,2-dimethyl-3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-ylmethoxy)phenyl]hex-4-ynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC(C(C)=O)(C(=O)OC)C(C=O)CC(=O)OC
Reaction #74821
compound ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC(C(C)=O)(C(=O)OC(C)(C)C)C(C=O)CC(=O)OC
Reaction #74823
compound ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74824
compound ( 2-a )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74825
compound ( 2-b )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(=O)C=CC1CC(=O)OC
Reaction #74826
compound ( 2-b )
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC1(C(=O)OC)C(O)CCC1CC(=O)OC
Reaction #74827
compound ( 1-a )
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCC1(C(=O)OC(C)(C)C)C(O)CCC1CC(=O)OC
Reaction #74828
compound ( 1-a )
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC(C)(C)C)C(O)CCC1CC(=O)OC
Reaction #74831
compound ( 1-b )
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC#Cc1ccc(OCCCC/C=C/c2ccc(OC)cc2)c(CCC(=O)OC)n1
Reaction #83543
5-{2-(2-methoxycarbonylethyl)-3-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]-6-pyridyl}-4-pentynoic acid methyl ester
المردود 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC#Cc1ccc(O)c(CCC(=O)OC)n1
Reaction #83588
5-[3-hydroxy-2-(2-methoxycarbonylethyl)-6-pyridyl]-4-pentynoic acid methyl ester
المردود 84.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCc1ccc(O)c(CCC(=O)OC)n1
Reaction #83589
5-[3-hydroxy-2-(2-methoxycarbonylethyl)-6-pyridyl]-pentanoic acid methyl ester
المردود 65.6%DOI: 10.6084/m9.figshare.5104873.v1
CC#CCC(C(=O)OCC)C(=O)OCC
Reaction #87979
title intermediate
المردود 115.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](N)CC#Cc1cc(-c2ccc(F)cc2C)c(N(C)C(=O)C(C)(C)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cn1
Reaction #156719
title compound
المردود 89.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CCC(c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)=N1
Reaction #156720
title compound
المردود 118.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](N)CC#Cc1cc(-c2ccc(F)cc2C)c(N(C)C(=O)C(C)(C)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cn1
Reaction #156721
Intermediate 13
DOI: 10.6084/m9.figshare.5104873.v1
C#CC[C@@](C)(N)C(=O)OC
Reaction #156723
methyl (2R)-2-amino-2-methylpent-4-ynoate
DOI: 10.6084/m9.figshare.5104873.v1
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