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474785

CCOC(=O)c1cc2cc(C(=O)N3CCCN(C(=O)OC(C)(C)C)CC3)ccc2n1C(C)C
Reaction #194031
DOI: 10.1039/C8SC04228D
CC(C)n1c(C(=O)N2CCN(S(C)(=O)=O)CC2)cc2cc(C(=O)N3CCCN(C(=O)OC(C)(C)C)CC3)ccc21
Reaction #203514
DOI: 10.1039/C8SC04228D
CC(C)n1c(C(=O)O)cc2cc(OCc3ccccc3)ccc21
Reaction #236765
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(C(=O)N3CCCC(N(C)C)C3)ccc2n1C(C)C
Reaction #240809
DOI: 10.1039/C8SC04228D
O=C(O)c1cc2cc(Br)ccc2n1C(c1ccccc1)c1ccccc1
Reaction #256320
DOI: 10.1039/C8SC04228D
CC(C)n1c(C(=O)N2CCC(F)(F)CC2)cc2cc(C(=O)N3CCCC(N(C)C)C3)ccc21
Reaction #290179
DOI: 10.1039/C8SC04228D
CC(C)n1c(C(=O)N2CCN(C(=O)N(C)C)CC2)cc2cc(C(=O)N3CCCN(C(=O)OC(C)(C)C)CC3)ccc21
Reaction #376516
DOI: 10.1039/C8SC04228D
CC(C)n1c(C(=O)O)cc2cc(C(=O)N3CCCN(C(=O)OC(C)(C)C)CC3)ccc21
Reaction #384994
DOI: 10.1039/C8SC04228D
O=C(O)c1cc2cc(-c3cccs3)ccc2n1C(c1ccccc1)c1ccccc1
Reaction #394952
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(OCc3ccccc3)ccc2n1C(C)C
Reaction #581185
desired product
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(C(=O)O)cc2cc(OCc3ccccc3)ccc21
Reaction #581186
desired product
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(C(=O)O)cc2cc(O)ccc21
Reaction #581187
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(C(=O)N2CCS(=O)(=O)CC2)cc2cc(O)ccc21
Reaction #581188
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cccc3c2n1[C@H](C1CCCCC1)CO3
Reaction #587622
ethyl (R)-3-cyclohexyl-2,3-dihydropyrrolo[1,2,3-de]-1,4-benzoxazine-5-carboxylate
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c3c(c1)ccn3[C@H](C1CCCCC1)CO2
Reaction #587623
(R)-3-cyclohexyl-2,3-dihydropyrrolo[1,2,3-de]-1,4-benzoxazine
Ausbeute 85.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CNC(=O)c2cc3cc(O)ccc3n21
Reaction #593834
desired product
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(OCc3ccccc3)ccc2n1[C@@H](C)CNC(=O)OC(C)(C)C
Reaction #593840
desired compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(C)(C)C(O[SiH](C)C)[C@@H]1CNC(=O)c2cc3cc(OCc4ccccc4)ccc3n21
Reaction #593843
desired product
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc4n(c3cc2Br)[C@H](C)CNC4=O)CC1
Reaction #593941
product
Ausbeute 31.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(OC3CCN(C(C)C)CC3)c(Br)cc2n1[C@H](C)CNC(=O)OC(C)(C)C
Reaction #593942
desired compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
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