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OCCCCBr

CCOC(=O)CC(C)COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2339
ethyl 3-methyl-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(C)Oc1ccc(Oc2ccc(Cl)cc2F)cc1
Reaction #4556
ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCc1cc2nc3ccc(O[C@@H]4O[C@H](COC(C)=O)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@H]4OC(C)=O)cc3oc-2cc1=O
Reaction #4976
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCN1CCCN(Cc2ccc(OCc3ccccc3)cc2)CC1
Reaction #44793
methyl hexahydro-4-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine-1-butanoate
المردود 79.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OC[C@@H]1OC(=O)[C@H]2OC(C)(C)O[C@@H]12
Reaction #48950
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COCCCCBr
Reaction #51242
(4-Bromo-butoxy)-acetic Acid Ethyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(F)c(F)c1)[C@H]1CC[C@H](OCCCCBr)CC1
Reaction #53821
trans-[4-(4-bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 3,4-difluoro-phenyl ester
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](OCCCCBr)CC1
Reaction #53823
trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(F)cc1F)[C@H]1CC[C@H](OCCCCBr)CC1
Reaction #53831
trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 2,4-difluoro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)N(C)[C@H]1CC[C@H](OCCCCBr)CC1
Reaction #53832
trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-carbamic acid isobutyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCBr)COC1CCCCO1
Reaction #55634
1-bromo-3-methyl-4-(tetrahydropyran-2-yloxy)-butane
المردود 65741.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCOc1ccc(C=O)cc1OC
Reaction #62264
keto-ester
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1ccccc1)OC(=O)C[C@H]1C[C@@H](CBr)OC(C)(C)O1
Reaction #67679
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(=O)C(C)Br
Reaction #71795
Methyl 4-bromo-3-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(CC(=O)OC)c(C)s3)C[C@H]2OC)nc1Cl
Reaction #71797
title compound
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #74254
17
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C1C#CCCCCC1
Reaction #74255
cyclooct-1-yn-3-glycolic acid
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(Br)C(=O)CC(=O)OC
Reaction #86500
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(Br)c1cc(=O)n2c(C)cccc2n1
Reaction #86501
desired product
المردود 64.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(=O)C(C)Br
Reaction #86512
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي