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O=C1CC=C(c2c[nH]c3cc([N+](=O)[O-])ccc23)CC1
Reaction #175515
DOI: 10.1039/C8SC04228D
Fc1cccc2[nH]cc(C3CCC4(CC3)OCCO4)c12
Reaction #188031
DOI: 10.1039/C8SC04228D
COc1ccccc1N1CCN(C2CC=C(c3c[nH]c4ccc(F)cc34)CC2)CC1
Reaction #195966
DOI: 10.1039/C8SC04228D
N#Cc1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #221745
DOI: 10.1039/C8SC04228D
Fc1ccc2c(C3=CCC4(CC3)OCCO4)c[nH]c2c1
Reaction #244459
DOI: 10.1039/C8SC04228D
Clc1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #253078
DOI: 10.1039/C8SC04228D
c1ccc2c(C3CCC4(CC3)OCCO4)c[nH]c2c1
Reaction #280231
DOI: 10.1039/C8SC04228D
O=C1CC=C(c2c[nH]c3ccc(F)cc23)CC1
Reaction #291842
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #381961
DOI: 10.1039/C8SC04228D
C1=C(c2c[nH]c3ccccc23)CCC2(C1)OCCO2
Reaction #387569
DOI: 10.1039/C8SC04228D
O=C1CC=C(c2c[nH]c3ccc([N+](=O)[O-])cc23)CC1
Reaction #393174
DOI: 10.1039/C8SC04228D
COc1ccccc1N1CCN(C2CC=C(c3c[nH]c4ccc(F)cc34)CC2)CC1
Reaction #404427
DOI: 10.1039/C8SC04228D
C1=C(c2c[nH]c3ccccc23)CCC2(C1)OCCO2
Reaction #515664
product
Rendimiento 89.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #515665
product
Rendimiento 87.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(C3=CCC4(CC3)OCCO4)c[nH]c2c1
Reaction #515666
title compound
Rendimiento 96.3%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #515667
title compound
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #515668
title compound
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #515669
title compound
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]cc(C3=CCC4(CC3)OCCO4)c2c1
Reaction #515670
3-(1,4-Dioxa-spiro[4,5]dec-7-en-8-yl)-5-methoxy-1H-indole
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1
C1=C(c2n[nH]c3ccccc23)CCC2(C1)OCCO2
Reaction #515671
3-(1,4-Dioxa-spiro[4,5]dec-7-en-8-yl)-1H-azaindole
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
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