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17469

COc1ccc(CCN)c(C)c1C
Reaction #6824
2-(4-methoxy-2,3-dimethylphenyl)ethylamine
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C(F)(F)F
Reaction #48762
trifluoroacetate
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@]1(O)C[C@H]2CN(CCc3c([nH]c4c(I)cccc34)[C@@](C(=O)OC)(c3cc4c(cc3OC)N(C)[C@H]3[C@@](O)(C(=O)OC)[C@H](OC(C)=O)[C@]5(CC)C=CCN6CC[C@]43[C@@H]65)C2)C1
Reaction #48763
12′-iodovinblastine
Ausbeute 112.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(C(=O)CN4CCCCC4)ccc3OCC)nc12
Reaction #50202
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](NC(=O)OC(C)(C)C)C(=O)O)cc1C
Reaction #61111
(R)-tert-butoxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(N)=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77805
5-carbamoylmethyl-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(=O)O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77806
aimed product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1-c1cccs1)C(C)CNCC2
Reaction #171276
yellow oil
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1C#N)C(C)CNCC2
Reaction #171278
white solid
Ausbeute 86.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1-c1cccs1)C(C)CNCC2
Reaction #186623
DOI: 10.1039/C8SC04228D
CC(C)(Cc1cccc(CC(=O)NC23CC4CC(CC(C4)C2)C3)c1)NCC(O[Si](C)(C)C(C)(C)C)c1ccc(OCc2ccccc2)c(CO)c1
Reaction #190035
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1C#N)C(C)CNCC2
Reaction #196641
DOI: 10.1039/C8SC04228D
CCN1CCN(CCc2ccc(OCc3ccccc3)c(C(=O)Nc3cc(-c4ccccc4)ccc3C(=O)OC(C)(C)C)c2)CC1
Reaction #196804
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(CC(N)CNS(C)(=O)=O)ccc1OCc1ccccc1
Reaction #199867
DOI: 10.1039/C8SC04228D
COc1c(C=O)c2c(c(Sc3ccccc3)c1OC)CCN(C)CC2
Reaction #199975
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)CN2CCN(c3ccccc3)CC2)cc1C(=O)O.Cl
Reaction #214658
2-methoxy-5-[2-(4-phenyl-1-piperazinyl)acetyl]benzoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CCNCc2ccccc2)ccc1Oc1ccc(C(N)=O)cn1
Reaction #217906
title compound
Ausbeute 96.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1Oc1nnnn1-c1ccccc1)C(c1ccccc1)CN(C)CC2
Reaction #228211
DOI: 10.1039/C8SC04228D
Oc1ccc2c(c1)CC(NCC(O)c1ccc(OCc3ccccc3)c(CCOCc3ccccc3)c1)CC2
Reaction #237153
DOI: 10.1039/C8SC04228D
CCNCCc1ccc(OCCNc2ncnc(C)c2Cl)c(C)c1
Reaction #237299
DOI: 10.1039/C8SC04228D
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