allyl bromide

C=CCn1c(=O)n(C)c(=O)n(-c2cc(N=c3sc(=O)n4n3CCCC4)c(F)cc2Cl)c1=O
Reaction #1585
title product
Выход 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)OC(C)(C)C
Reaction #2014
desired product
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC=COc1ccccc1C(C)(C)C
Reaction #3049
2-(1,1-dimethylethyl)phenoxypropene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOc1ccc(C(=O)OC)cc1
Reaction #3072
methyl 4-allyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3846
compound 37
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=CCOc1ccc2c(c1)C(=O)NC(C)(C)O2
Reaction #4644
2,3-dihydro-2,2-dimethyl-6-(1-propen-3-yloxy)-4H-1,3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=CCOc1cc(N)c(Cl)cc1C(=O)O
Reaction #5471
pale tan solid
Выход 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCn1ccc2ccccc21
Reaction #5695
1-allylindole
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCN(C)CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccccc21.O=C(O)C(=O)O
Reaction #5922
4-(N-allyl-N-methylaminoacetyl)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine oxalate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCN(C)CCCN1C(=O)C(c2ccc(Cl)cc2)Sc2ccc3ccccc3c21
Reaction #5933
1-[3-(N-allyl-N-methylamino)propyl]-3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCOc1ccc(C(=O)OC)cc1CC=C
Reaction #6024
title compound
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCC(C(=O)OC)C(=O)c1cccnc1
Reaction #6530
methyl-2-nicotinoyl-4-pentenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCC(C(=O)COC1CCCCC1)C(=O)OCC
Reaction #6595
Ethyl 2-(cyclohexyloxyacetyl)-4-pentenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)NC(=O)Nc1ccc(C(F)(F)F)cc1C(=O)O
Reaction #7769
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCC1CC2(CCCC)Cc3cc(OCOC)ccc3C2=C(C)C1=O
Reaction #7964
(2SR,9aSR)-2-allyl-9a-butyl-7-methoxymethoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCN1CCNCC1
Reaction #9029
piperazine
Выход 155.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCN(CC=C)Cc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1
Reaction #9033
foam
Выход 56.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCNCc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1
Reaction #9034
(4-allylaminomethyl-benzyl)-(1H-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCc1cc(OCc2ccccc2)cc(CC=C)c1O
Reaction #9351
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCn1c2ccc(OC)cc2c2c3c(c(-c4ccccc4Cl)cc21)C(=O)N(Cc1ccc(OC)cc1OC)C3=O
Reaction #11225
carbazole
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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