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38225

CC(C)(C)OC(=O)N1CCC[C@@H]1c1cc(F)ccc1F
Reaction #92249
(R)-tert-butyl 2-(2,5-difluorophenyl)pyrrolidine-1-carboxylate
Ausbeute 72.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1SC[C@H](Cc2ccccc2)N1C(=O)[C@H](Cn1nnc2ccccc2c1=O)[C@@H](O)CCc1ccc(-c2cc(F)cc(F)c2)cc1
Reaction #171233
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1SC[C@H](Cc2ccccc2)N1C(=O)[C@H](Cn1nnc2ccccc2c1=O)[C@@H](O)CCc1ccc(-c2ccc(F)cc2)cc1
Reaction #171237
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1NC(=S)N(C(C)(C)C)C1=O
Reaction #258899
DOI: 10.1039/C8SC04228D
B.CC(C)C1CC[C@H](C)CC1OP1CCC[C@@H]1Cc1ccccc1
Reaction #440217
(1S,2R)-2-benzyl-1-(−)-menthoxy-phospholane borane
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
B.CC(C)C1CC[C@H](C)CC1OP1CCC[C@@H]1Cc1ccccc1
Reaction #483128
(1S,2R)-2-benzyl-1-(−)-menthoxy-phospholane borane
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCCC[C@@H](C(=O)N1C(=O)OC[C@H]1Cc1ccccc1)[C@H](O)C=Cc1ccccc1)(c1ccccc1)c1ccccc1
Reaction #584661
desired product
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]1c1cc(F)ccc1F
Reaction #624933
(R)-tert-butyl 2-(2,5-difluorophenyl)pyrrolidine-1-carboxylate
Ausbeute 72.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H]2CCCN2C(=O)OC(C)(C)C)s1
Reaction #651401
(R)-tert-butyl 2-(5-methoxycarbonylthiophen-2-yl)pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@H](O)c1ccccc1
Reaction #671282
methyl (S)-(−)-3-hydroxy-3-phenylpropionate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]1c1cc(F)ccc1F
Reaction #675703
(R)-tert-butyl 2-(2,5-difluorophenyl)pyrrolidine-1-carboxylate
Ausbeute 72.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]1[C@@H](O)[C@H](Cc1ccccc1)N(Cc1ccccc1)Cc1ccccc1
Reaction #819529
title compound
Ausbeute 60.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@H](Cc2ccccc2)N(Cc2ccccc2)Cc2ccccc2)CCC1(C)C
Reaction #819556
title compound
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCC.FB(F)F
Reaction #836582
BF3.Et2O
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.c1cnc([C@H]2CCCN2)cn1
Reaction #1013567
(R)-2-pyrrolidin-2-yl-pyrazine hydrochloride
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
C1CCN2C[C@H]3C[C@H](CN4CCCC[C@@H]34)[C@H]2C1
Reaction #1138617
Sparteine
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCCC[C@@H](C(=O)N1C(=O)OC[C@H]1Cc1ccccc1)[C@H](O)C=Cc1ccccc1)(c1ccccc1)c1ccccc1
Reaction #1256409
desired product
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(F)cc1[C@H]1CCCN1C(=O)OC(C)(C)C
Reaction #1514070
(R)-tert-butyl 2-(5-fluoro-2-methoxypyridin-3-yl)pyrrolidine-1-carboxylate
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]1c1cc(F)cnc1Cl
Reaction #1514100
desired product
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([C@H]2CCCN2C(=O)OC(C)(C)C)c1
Reaction #1611482
(R)-2-(3-methoxycarbonyl-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
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