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COc1cccc(C)c1O

CC1(C)Oc2cc3c(c(C(O)(c4c5c(cc6c4SC(C)(C)S6)SC(C)(C)S5)c4c5c(cc6c4SC(C)(C)S6)SC(C)(C)S5)c2O1)OC(C)(C)O3
Reaction #2690
pure product
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c2c(c(C(O)(c3c4c(c(C(=O)OCC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c4c(c(C(=O)OCC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c1OC(C)(C)O3)OC(C)(C)O2
Reaction #2691
Bis-(8-ethoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole-4-yl)-mono-(8-ethoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dioxol-4-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2cc3c(c(C(O)(c4c5c(cc6c4OC(C)(C)O6)OC(C)(C)O5)c4c5c(cc6c4SC(C)(C)S6)SC(C)(C)S5)c2O1)OC(C)(C)O3
Reaction #2693
Bis-(2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dioxol-4-yl)-mono-(2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole-4-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2c(c(C(O)(c3c4c(c(C(=O)O)c5c3OC(C)(C)O5)OC(C)(C)O4)c3c4c(c(C(=O)O)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c(c2C(=O)O)OC(C)(C)O3)O1
Reaction #2694
Bis-(8-carboxy-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dioxol-4-yl)-mono-(8-carboxy-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiol-4-yl) methanol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c2c(c(C(c3c4c(c(C(=O)OC)c5c3OC(C)(C)O5)OC(C)(C)O4)c3c4c(c(C(=O)OC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c1OC(C)(C)O3)OC(C)(C)O2
Reaction #2695
Bis-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis (1,3) dioxol-4-yl)-mono-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiol-4-yl) methane
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(c2c[nH]c3c2CC=C(C(=O)O)C3)N(C)C)c1OC
Reaction #9151
3-[(2,3-Dimethoxy-phenyl)-dimethylamino-methyl]-4,7-dihydro-1H-indole-6-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(P(=O)(c2ccccc2)c2ccccc2)c(-c2ccccc2)c(OC)c1OC
Reaction #52142
product 22
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)C(C)=CC(C)(C)N3)c1OC
Reaction #54097
6-(2,3-dimethoxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinoline
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC(=O)c1ccc(OC)c(OC)c1OC
Reaction #62231
product
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)CCCC(=O)O)c(OC)c1OC
Reaction #62232
61
Выход 109.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OC(C)CC2=O
Reaction #62723
title compound
Выход 29.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(C(=O)C3COc4ccc(O)cc4O3)CC2)c(OC)c1OC
Reaction #65456
7-HYDROXY-2-[4-(2,3,4-TRIMETHOXYBENZYL)PIPERAZIN-1-YLCARBONYL]-2,3-DIHYDRO-1,4-BENZODIOXIN
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1C(=O)c2ccc(OC)c(OC)c2CC1c1ccccc1
Reaction #82413
title compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2n[nH]c3ncnc(Nc4cccc(Cl)c4)c23)c(OC)c1OC
Reaction #176900
DOI: 10.1039/C8SC04228D
COc1cc(C)c(CCCC(=O)O)c(O)c1OC
Reaction #180641
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(-c2c(OC)ccc(O)c2OC)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #181576
DOI: 10.1039/C8SC04228D
CCOc1c2c(c([N+](=O)[O-])c(OCC)c1OCC)C(=O)OC2
Reaction #183689
DOI: 10.1039/C8SC04228D
CCOC(=O)CCc1ccc(Cc2c(C)c(OC)c(OC)c(OC)c2OC)cc1
Reaction #186464
DOI: 10.1039/C8SC04228D
COc1c(C)c(Cc2ccc(OCc3ccccc3)c(C(=O)O)c2)c(OC)c(OC)c1OC
Reaction #188022
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)Cc2c(Cl)cncc2Cl)c(O)c1OC
Reaction #195390
DOI: 10.1039/C8SC04228D
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