部分構造検索

302854

CCCCCCCCCCCCc1ccc(N=Nc2ccc(OCCCCCCCCCCBr)cc2)cc1
Reaction #5849
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCc1ccc(N=Nc2ccc(OCCCCCCCCCCBr)cc2)cc1
Reaction #5850
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=O)ccc1OCCCCCCCCCCOc1ccc(C=O)cc1OC
Reaction #6290
compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCCBr
Reaction #9894
11-bromo-undec-1-ene
収率 82.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9895
(S)-3-(1-methyl-pyrrolidin-2-yl)-1-undec-10-enyl-pyridinium bromide
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
BrCCCCCCC1CCCCC1
Reaction #9908
(6-bromo-hexyl)-cyclohexane
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN1CCC[C@H]1c1ccc[n+](CCCCCCC2CCCCC2)c1.[Br-]
Reaction #9909
(S)-1-(6-cyclohexyl-hexyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt
収率 63.3%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N(CCCCCCCCCCBr)n2cnnc2)cc1
Reaction #11985
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](Br)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40600
36
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N=[N+]=[N-])C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40601
38
収率 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC=Cc1cccc(OC)c1
Reaction #46727
pure product
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1oc2ccc(Cl)cc2c(=O)n1CCCCCCCCCCBr
Reaction #47722
6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione
収率 49.9%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N(CCCCCCCCCCBr)n2cnnc2)cc1
Reaction #48187
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCCOc1ccc(C(=O)OC)cc1
Reaction #49716
Methyl 4-docosyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)C(=O)CC[C@@H]12
Reaction #50340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)OB(O)c1ccc(CCCCCCCCCCCO)cc1
Reaction #53274
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53928
trans-4-(5-Bromo-pentyl)-cyclohexylamine
収率 129.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(N[C@H]1CC[C@H](CCCCCBr)CC1)c1ccc(C(F)(F)F)cc1
Reaction #53929
trans-N-[4-(5-Bromo-pentyl)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53935
trans-[4-(5-Bromo-pentyl)-cyclohexyl]-methyl-amine hydrobromide
収率 179.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1CC[C@H](CCCOc2ccc(C=O)cc2)CC1
Reaction #64066
4-[3-(trans-4-pentylcyclohexyl)-1-propyloxy]benzaldehyde
収率 121.9%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ