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C1CCOC(C1)OCCCCBr

CCCCCCCC/C=C\CCCCCCCC(=O)OCCCCOC1CCCCO1
Reaction #5348
(Z)-9-octadecenoic acid 4-[(tetrahydro-2H-pyran-2-yl)oxy]butyl ester
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
BrCCCCOC1CCCCO1
Reaction #6684
2-(4-bromobutoxy) -tetrahydropyran
DOI: 10.6084/m9.figshare.5104873.v1
BrCCCCOC1CCCCO1
Reaction #6690
2-(4-bromobutoxy)-tetrahydropyran
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCBr)COC1CCCCO1
Reaction #55634
1-bromo-3-methyl-4-(tetrahydropyran-2-yloxy)-butane
Ausbeute 65741.3%DOI: 10.6084/m9.figshare.5104873.v1
BrCCCCOC1CCCCO1
Reaction #67524
product 2
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@H](Br)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@H]1O[C@H](COC(C)=O)[C@@H](O[C@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #162027
bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](N=[N+]=[N-])[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@H]1O[C@H](COC(C)=O)[C@@H](O[C@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #162028
azide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC[C@H]1O[C@@H](N=C=S)[C@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1O[C@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](O[C@H]2O[C@H](COC(=O)c3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](OC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162040
white solid
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O
Reaction #191410
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O
Reaction #229295
DOI: 10.1039/C8SC04228D
BrCCCCOC1CCCCO1
Reaction #229418
DOI: 10.1039/C8SC04228D
—
Reaction #345564
XXXVII
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@H](Br)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@@H]1O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #348049
α-D-Cellobiosyl bromide heptaacetate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #362377
XXXVII
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC=CCCCCCCCC(=O)OCCCCOC1CCCCO1
Reaction #389639
DOI: 10.1039/C8SC04228D
BrCCCCOC1CCCCO1
Reaction #443411
4-(tetrahydropyran-2-yl)oxybutyl bromide
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #460871
XXXVII
DOI: 10.6084/m9.figshare.5104873.v1
CC(CBr)CCOC1CCCCO1
Reaction #564464
2-[4-bromo-3-methylbutoxy]-tetrahydro-2H-pyran
Ausbeute 64.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #571382
XXXVII
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(CCCCOC2CCCCO2)CC1
Reaction #618108
title compound
Ausbeute 48.9%DOI: 10.6084/m9.figshare.5104873.v1
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