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CCCCP(CCCC)CCCC

COC(=O)c1cc(N2CCOCC2)cc2c1nc(C)n2Cc1cccc(C(F)(F)F)c1C
Reaction #582
Ausbeute 0.0%
CCOC(=O)C1=C(CSCCN)NC(C)=C(C(=O)OC)C1c1cccc([N+](=O)[O-])c1.O=C(O)/C=C/C(=O)O
Reaction #5745
(-)-2-(aminoethylthio)methyl-3-carboethoxy-5-carbomethoxy-4-(3-nitrophenyl)-6-methyl-1,4-dihydropyridine fumarate
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCO)c1ccc(C=CC=O)cc1
Reaction #6294
cinnamaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCCO)c1ccc(C=CC=O)cc1
Reaction #6298
compound A
DOI: 10.6084/m9.figshare.5104873.v1
O=CC=Cc1ccc2c(c1)CCCN2CCCCCCO
Reaction #6304
3-(N-hydroxyhexyl-1,2,3,4-tetrahydroquinolin-6-yl)acrolein
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(Cc2ccoc2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Cl)cnnc2cc1OCc1ccncc1.Cl
Reaction #7572
4-chloro-6-methoxy-7-(4-pyridylmethoxy)cinnoline hydrochloride
Ausbeute 122.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(N2CCOCC2)c(F)c1
Reaction #8238
oil
Ausbeute 331.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8240
solid
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2ccnc2)c(F)c1
Reaction #8243
desired product
Ausbeute 158.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2cnc(CO)c2)c(F)c1
Reaction #8245
desired product
Ausbeute 13.9%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2nn3c(c2-c2ccnc4ccccc24)OCC3)nc1
Reaction #8376
title compound
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(OCCc2cccs2)cc1C
Reaction #9749
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(SCc2coc(-c3ccc(C(F)(F)F)cc3)c2)cc1C
Reaction #9785
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCN(CCCc1ccccc1)S(=O)(=O)c1cccc2cnccc12
Reaction #10587
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCOc1cccc2c(Cl)nccc12
Reaction #10597
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O[C@H]2CC[C@@H](NC(=O)OC(C)(C)C)CC2)cc1
Reaction #10659
title compound
Ausbeute 96.3%DOI: 10.6084/m9.figshare.5104873.v1
C1CCC([PH+](C2CCCCC2)C2CCCCC2)CC1.c1ccc([B-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #42144
tricyclohexylphosphonium tetraphenylborate
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[PH+](CCCC)CCCC.c1ccc([B-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #42146
tri-n-butylphosphonium tetraphenylborate
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCc1ccccc1
Reaction #42152
1-phenylheptane
DOI: 10.6084/m9.figshare.5104873.v1
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