部分構造検索

44823

CC1(c2ccc3c(C4CC4)c(OC4CCC(C(C)(C)C)CC4)ccc3c2)COC(=O)N1
Reaction #227079
DOI: 10.1039/C8SC04228D
CC(N)(CO)c1ccc2c(Br)c(OC3CCC(C(C)(C)C)CC3)ccc2c1
Reaction #271724
DOI: 10.1039/C8SC04228D
CC1(c2ccc3c(-c4ccc(OC(F)(F)F)cc4)c(OC4CCC(C(C)(C)C)CC4)ccc3c2)COC(=O)N1
Reaction #300012
DOI: 10.1039/C8SC04228D
CC1(c2ccc3c(Br)c(OC4CCC(C(C)(C)C)CC4)ccc3c2)COC(=O)N1
Reaction #374603
DOI: 10.1039/C8SC04228D
CC1(c2ccc3c(Cl)c(OC4CCC(C(C)(C)C)CC4)ccc3c2)COC(=O)N1
Reaction #891080
DOI: 10.1039/C8SC04228D
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2Br)CC1
Reaction #1123659
title compound
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2C2CC2)CC1
Reaction #1123660
title compound
収率 58.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2-c2ccc(OC(F)(F)F)cc2)CC1
Reaction #1123665
title compound
収率 83.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2Cl)CC1
Reaction #1123680
(R)-4-(6-(trans-4-tert-butylcyclohexyloxy)-5-chloronaphthalen-2-yl)-4-methyloxazolidin-2-one
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@@](C)(N)CO)ccc3c2Br)CC1
Reaction #1123682
(R)-2-amino-2-(5-bromo-6-(trans-4-tert-butylcyclohexyloxy)naphthalen-2-yl)propan-1-ol
収率 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc3c(-c4ccc(OC(F)(F)F)cc4)c(OC4CCC(C(C)(C)C)CC4)ccc3c2)COC(=O)N1
Reaction #1225969
DOI: 10.1039/C8SC04228D
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2Br)CC1
Reaction #2476319
title compound
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2C2CC2)CC1
Reaction #2476320
title compound
収率 58.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2-c2ccc(OC(F)(F)F)cc2)CC1
Reaction #2476325
title compound
収率 83.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@]4(C)COC(=O)N4)ccc3c2Cl)CC1
Reaction #2476340
(R)-4-(6-(trans-4-tert-butylcyclohexyloxy)-5-chloronaphthalen-2-yl)-4-methyloxazolidin-2-one
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3cc([C@@](C)(N)CO)ccc3c2Br)CC1
Reaction #2476342
(R)-2-amino-2-(5-bromo-6-(trans-4-tert-butylcyclohexyloxy)naphthalen-2-yl)propan-1-ol
収率 31.0%DOI: 10.6084/m9.figshare.5104873.v1