بحث البنية الفرعية

c1ccc(CC2CCCN2)cc1

CC1(C(F)(F)F)C[C@@H](O)c2cc(Br)ccc2O1
Reaction #48333
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC1CCC2C3CC=C4CC(OC(=O)NCCCCCC(=O)N5CC(OC(=O)CCC(=O)O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49173
compound 8
المردود 89.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCOCC(COC(=O)NCCCCCC(=O)N1CC(OC(=O)CCC(=O)O)CC1C(OC(c1ccc(OC)cc1)c1ccc(OC)cc1)c1ccccc1)OCCCCCCCCCCCCCCCCCC
Reaction #49174
compound 14
المردود 47.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC1(C)CCc2c(C)c(OCCOC(=O)NCCCCCC(=O)N3CC(O)CC3C(OC(c3ccc(OC)cc3)c3ccc(OC)cc3)c3ccccc3)c(C)c(C)c2O1
Reaction #49176
Compound 19
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC1(C)CCc2c(C)c(OCCOC(=O)NCCCCCC(=O)N3CC(OC(=O)CCC(=O)O)CC3C(OC(c3ccc(OC)cc3)c3ccc(OC)cc3)c3ccccc3)c(C)c(C)c2O1
Reaction #49177
compound 21
المردود 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(OC(=O)CCC(=O)O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49206
compound 86
المردود 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49209
Compound 90
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@H]1CCC(=O)N1CCSCCCC(=O)OC
Reaction #51247
4-[(2-{(2R)-2-[(1E,3S)-3-hydroxyoct-1-enyl]-5-oxopyrrolidin-1-yl}ethyl)thio]butanoic acid methyl ester
المردود 29.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@H]1CCC(=O)N1CCCCOCC(=O)OC
Reaction #51252
{4-[(R)-2-((E)-(S)-3-hydroxy-oct-1-enyl)-5-oxo-pyrrolidin-1-yl]-butoxy}-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CCN2C(=O)CC[C@@H]2/C=C/[C@H](O)CCC[C@@H](C)O[Si](C)(C)C(C)(C)C)cc1
Reaction #57059
Methyl 4-{2-[(2R)-2((1E,3R,7R)-7-{[tert-butyl(dimethyl)silyl]oxy}-3-hydroxyoct-1-enyl)-5-oxopyrrolidin-1-yl}ethyl}benzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Oc1ccc2c(c1)CCCC2O)C(F)(F)F
Reaction #60381
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ncnc2cc(C(=O)N3CCC[C@H]3C(c3ccccc3)c3ccccc3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1
Reaction #62457
7-[(2S)-2-benzhydryl-pyrrolidin-1-yl-carbonyl]-6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCC[C@H](O)c1ccc(F)cc1
Reaction #66006
methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoate
المردود 98.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)cnc1N1CCCC1Cc1ccccc1
Reaction #159640
title compound ( D100 )
المردود 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H]([C@@H](C(=O)O)c2ccc(Br)cc2)CCC1(C)C
Reaction #166676
(S)-2-(4-bromophenyl)-2-((S)-1-(tert-butoxycarbonyl)-5,5-dimethylpyrrolidin-2-yl)acetic acid
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H]([C@@H](C(=O)[O-])c2ccc(Cl)c(F)c2)CCC1(C)C.[Na+]
Reaction #166678
(S)-2-((S)-1-(tert-butoxycarbonyl)-5,5-dimethylpyrrolidin-2-yl)-2-(4-chloro-3-fluorophenyl)acetic acid sodium salt
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]1[C@@H](C(=O)O)c1ccc(Cl)cc1
Reaction #166684
(S)-2-((S)-1-(tert-butoxycarbonyl)-pyrrolidin-2-yl)-2-(4-chlorophenyl)acetic acid
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H]([C@@H](C(=O)N2C(=O)OC[C@H]2Cc2ccccc2)c2ccc(Cl)cc2)CCC1(C)C
Reaction #166685
(S)-tert-butyl 5-((S)-2-((R)-4-benzyl-2-oxooxazolidin-3-yl)-1-(4-chlorophenyl)-2-oxoethyl)-2,2-dimethylpyrrolidine-1-carboxylate
المردود 90.9%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC(Cc2ccc(-c3ccccc3)cc2)NC1=O
Reaction #174972
DOI: 10.1039/C8SC04228D
CCC(C)(C)CC(O)CNC(=O)C1(Cc2ccc(-c3ccc(F)cn3)cc2)CCCN1C(=O)OC(C)(C)C
Reaction #175850
DOI: 10.1039/C8SC04228D
الصفحة 1التالي