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803969

CCCC(=O)OC[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)CO1
Reaction #48621
desired compound
収率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](COc2ccccc2)CN1C(=O)OC(C)(C)C
Reaction #48655
title compound
収率 45.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CO)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48656
desired compound
収率 88.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](COC2CCCCC2)OC[C@@H]1[C@@H](OCc1ccccc1)[C@H](Cc1cc(F)cc(F)c1)N(Cc1ccccc1)Cc1ccccc1
Reaction #48659
desired compound
収率 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](COC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48660
desired compound
収率 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)/C=C(\C)C(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](COC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48661
title compound
収率 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OC[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(C)=O)CO1.Cl
Reaction #48755
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
OC(C1CC1)C1CN(Cc2ccccc2)CCO1
Reaction #58600
76
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C1CC1)C1CN(Cc2ccccc2)CCO1
Reaction #58601
Cyclopropyl[4-(phenylmethyl)morpholin-2-yl]methanone
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #58604
base
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1CC(O)(C1CCOCC1)C1CNCCO1.Cl
Reaction #58605
compound 52b
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #58606
solid
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.OC(Cc1ccccc1-c1ccccc1)(C1CCOCC1)C1CNCCO1
Reaction #58607
56
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCO[C@@H](CN2C(=O)c3ccccc3C2=O)C1
Reaction #69376
(S)-tert-butyl 2-((1,3-dioxoisoindolin-2-yl)methyl)morpholine-4-carboxylate
収率 51.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCO[C@H](COS(C)(=O)=O)C1
Reaction #69378
(S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCO[C@H](CN2C(=O)c3ccccc3C2=O)C1
Reaction #69379
title compound
収率 86388.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C(C)(C)C)CC(CO)O2
Reaction #160097
tert-butyl 8-tert-butyl-10-(hydroxymethyl)-11-oxa-3,8-diazaspiro[5.5]undecane-3-carboxylate
収率 71.2%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CN(C(C)(C)C)CC2(CCN(C(=O)OC(C)(C)C)CC2)O1
Reaction #160098
tert-butyl 8-tert-butyl-10-(methoxymethyl)-11-oxa-3,8-diazaspiro[5.5]undecane-3-carboxylate
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CN(C(C)(C)C)CC2(CCNCC2)O1
Reaction #160099
8-tert-butyl-10-(methoxymethyl)-11-oxa-3,8-diazaspiro[5.5]undecane
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CN(CC(C)(F)F)CC2(CCNCC2)O1.Cl
Reaction #160102
4-(2,2-difluoropropyl)-2-(methoxymethyl)-1-oxa-4,9-diazaspiro[5.5]undecane hydrochloride
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
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