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CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(SC2CNC(=O)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #5160
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)CCOc1ccccc1N(C)C(=O)c1ccc(Cl)c(-c2cnc(C(F)(F)F)cc2C#N)c1)OC(=O)OC1CCCCC1
Reaction #174967
DOI: 10.1039/C8SC04228D
CC(Cl)OC(=O)OC1CCCCC1
Reaction #228508
DOI: 10.1039/C8SC04228D
CC(OC(=O)OC1CCCCC1)OC(=O)c1ccc(-c2ccccc2C(C)OCC(O)CNC(C)(C)Cc2ccc3ccccc3c2)cc1
Reaction #253290
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N[C@@H](CC(=O)N1CCn2c(C(F)(F)F)nc(C(=O)OCCOC(=O)OC3CCCCC3)c2C1)Cc1cc(F)c(F)cc1F
Reaction #308686
(R)-7-[3-tert-butoxycarbonylamino-4-(2,4,5-trifluoro-phenyl)-butyryl]-3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine-1-carboxylic acid (1-cyclohexyloxycarbonyloxy)-ethyl ester
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(C)cc(-c3cn4c(n3)CCCC4)cc2n1Cc1ccc(-c2ccccc2C(=O)OC(C)OC(=O)OC2CCCCC2)cc1
Reaction #320189
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(OCCOC(=O)c1cccc2c1CC(=CCCN1CCC(O)(c3ccc(Cl)cc3)CC1)c1cccnc1O2)OC1CCCCC1
Reaction #329723
titled compound
Ausbeute 116.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)OC1CCCCCCC1
Reaction #345768
Methyl cyclooctyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(I)OC(=O)OC1CCCCC1
Reaction #371321
DOI: 10.1039/C8SC04228D
CCC(I)OC(=O)OC1CCCC1
Reaction #387084
DOI: 10.1039/C8SC04228D
CCCc1nc2c(C)cc(-c3cn4c(n3)CCCC4)cc2n1Cc1ccc(-c2ccccc2C(=O)OC(C)OC(=O)OC2CCCCC2)cc1
Reaction #394953
DOI: 10.1039/C8SC04228D
CC(OC(=O)OC1CCCCC1)OC(=O)[C@H](CO)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)c1cnn[nH]1
Reaction #535782
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)[C@](C)(CO)C[C@H](N)Cc1ccc(-c2ccccc2)cc1
Reaction #535826
(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)CCOc1ccccc1N(C)C(=O)c1ccc(Cl)c(-c2cnc(C(F)(F)F)cc2C#N)c1)OC(=O)OC1CCCCC1
Reaction #536117
3-(2-{[4-Chloro-3-(4-cyano-6-trifluoromethyl-pyridin-3-yl)-benzoyl]-methyl-amino}-phenoxy)-propionic acid 1-cyclohexyloxycarbonyloxy-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(OCCOC(=O)c1cccc2c1CC(=CCCN1CCC(O)(c3ccc(Cl)cc3)CC1)c1cccnc1O2)OC1CCCCC1
Reaction #544234
titled compound
Ausbeute 116.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)OC(=O)OC1CCCCC1
Reaction #588959
1-chloroethyl cyclohexyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(I)OC(=O)OC1CCCCC1
Reaction #588960
cyclohexyl 1-iodoethyl carbonate
Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)[C@H](CO)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)c1cnn[nH]1
Reaction #610567
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)[C@](C)(CO)C[C@H](N)Cc1ccc(-c2ccccc2)cc1
Reaction #610609
(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)[C@H](CO)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)c1cnn[nH]1
Reaction #622342
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
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