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335626

O=C(Cl)OC1C2CC3CC(C2)CC1C3
Reaction #83115
2-Adamantylchloroformate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@](C)(Cc1c[nH]c2ccccc12)NC(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83116
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[O-]
Reaction #83122
carbonate
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1c[nH]c2ccccc12)N(COC(C)[Si](C)(C)C)C(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83139
title compound
Ausbeute 67.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C12CC3CC(C1)C(OC(=O)Cl)C(C3)C2
Reaction #159295
1-(methoxycarbonyl)-4-adamantyl chloroformate
Ausbeute 272.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1CN(C(=O)OC2C3CC4CC(C3)CC2C4)C1
Reaction #159308
title compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OC(=O)OC2CCN(C(c3cnc(NC(=O)C4(c5ccc6c(c5)OCO6)CC4)s3)c3ccccc3Cl)C2)C1
Reaction #208756
DOI: 10.1039/C8SC04228D
CC(c1c[nH]c2ccccc12)C(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)O
Reaction #229316
DOI: 10.1039/C8SC04228D
CC1CCC(C(C)C)C(OC(=O)N2CCc3ccccc3C2c2ccc(C(F)(F)F)cc2)C1
Reaction #255587
DOI: 10.1039/C8SC04228D
O=C(OCC1CCCCCCCCCC1)n1c(-c2cscn2)nc2ccccc21
Reaction #273607
DOI: 10.1039/C8SC04228D
CCCCC(CC)COC(=O)ON=C(N)c1cccc(CONC(=O)C2c3ccccc3C(=O)N(C3CCCCC3NS(C)(=O)=O)C2c2ccc(Cl)cc2Cl)c1
Reaction #281757
DOI: 10.1039/C8SC04228D
O=C(Cl)OC1C2CC3CC(C2)CC1C3
Reaction #320812
2-adamantylchloroformate
Ausbeute 251.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1c[nH]c2ccccc12)C(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)O
Reaction #320813
2-(2-adamantyloxycarbonyl)amino-3-(3-indolyl) butanoic acid
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #358496
white solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O[C@H]1CN2CCC1CC2)N(Cc1ccccc1)c1ccccc1
Reaction #358497
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(OC)C(=O)OC1C2CC3CC(C2)CC1C3
Reaction #368042
Dimethyl 2-adamantoxycarbonylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)OC1C2CC3CC(C2)CC1C3
Reaction #368053
2-adamantanyl chloroformate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)OCC1CCCC1
Reaction #368054
cyclopentylmethyl chloroformate
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OC(=O)Cl)C1
Reaction #383087
DOI: 10.1039/C8SC04228D
COc1ccc(CN2C(=O)C(NC(=O)OC3CC(C)CCC3C(C)C)c3ccccc3-c3ccccc32)cc1
Reaction #398664
DOI: 10.1039/C8SC04228D
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