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320509

O=C(NCCCCl)N1CCCC2CCCCC21
Reaction #67496
intermediate
Rendimiento 84.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C2CC3CC(C2)CC1C3)N1CCN(c2ccc(OCc3ncccn3)cc2)c2ccccc21
Reaction #69968
4-[4-(pyrimidin-2-ylmethoxy)phenyl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid adamantan-2-ylamide
Rendimiento 57.9%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@H]21
Reaction #76282
lovastatin
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79374
compounds A
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCN(C(=O)NC2C3CC4CC(C3)CC2C4)C1
Reaction #159316
(R)-tert-butyl 1-(2-adamantylcarbamoyl)pyrrolidin-3-ylcarbamate
Rendimiento 19.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H]1CCN(C(=O)NC2C3CC4CC(C3)CC2C4)C1
Reaction #159317
(R)-methyl 1-(2-adamantylcarbamoyl)pyrrolidin-3-ylcarbamate
Rendimiento 49.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@@H]1CN(CC23CC4CC(CC(C4)C2)C3)C(=O)N1)(c1ccccc1)c1ccccc1
Reaction #162342
(S)-4-((tert-butyldiphenylsilyloxy)methyl)-1-(1-adamantylmethyl)imidazolidin-2-one
Rendimiento 156.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@H](CO)CN1CC12CC3CC(CC(C3)C1)C2
Reaction #162343
(S)-1-(1-adamantylmethyl)-4-(hydroxymethyl)imidazolidin-2-one
Rendimiento 32.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1(CO)CN(CC23CC4CC(CC(C4)C2)C3)C(=O)N1
Reaction #162349
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)NCC(C)(C)N3CCOCC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172739
title compound
Rendimiento 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)N3CCN([C@@H]4COC[C@H]4N(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172740
title compound
Rendimiento 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(C2C3CC4CC(C3)CC2C4)C(=O)N1
Reaction #173504
DOI: 10.1039/C8SC04228D
CNCC(CC1CCCCC1)NC(=O)N1CCCC(C(CCCCOC)(NC(=O)C(C)C)c2cccc(Cl)c2F)C1
Reaction #181702
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCC12CCCCC1(Cc1ccc(C#N)cc1)NC(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #184383
DOI: 10.1039/C8SC04228D
CCN(CC)CCCCC1CCCN(C(=O)N2c3ccccc3C(=O)Nc3cccnc32)C1
Reaction #185519
DOI: 10.1039/C8SC04228D
O=C(NCC12CC3CC(CC(C3)C1)C2)n1cc(F)c(=O)[nH]c1=O
Reaction #191255
DOI: 10.1039/C8SC04228D
CC(=O)OC12CC3CC(C1)C(NC(=O)N1CCCC(C)C1)C(C3)C2
Reaction #192492
DOI: 10.1039/C8SC04228D
Cc1ccccc1C1C(OC(COC(=O)c2ccccc2)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CCC2CN(C3=NC(=O)CO3)CC21
Reaction #203904
DOI: 10.1039/C8SC04228D
O=C1Nc2cccnc2N(C(=O)N2CCCC(CCCCN3CCCC3)C2)c2ccccc21
Reaction #207544
DOI: 10.1039/C8SC04228D
CC(C)N1C(=O)N(C2C3CC4CC(C3)CC2C4)C(=O)C1c1ccccc1
Reaction #221308
DOI: 10.1039/C8SC04228D
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