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COC(=O)C1(C)CC(C)(C)CN1
Reaction #173732
DOI: 10.1039/C8SC04228D
COC(=O)C1(C)CC(C)(C)CN1C(=O)OC(C)(C)C
Reaction #252896
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(C)CC(C)(C)CN1C(=O)OC(C)(C)C
Reaction #580312
( 163E )
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)CC(C)(C)CN1c1nc(Cl)nc(Nc2cc(C3CC3)[nH]n2)n1
Reaction #1316568
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(C)CC(C)(C)CN1C(=O)OC(C)(C)C
Reaction #1447552
( 163E )
Rendimiento 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)CC(C)(C)CN1C(=O)OC(C)(C)C
Reaction #2048585
(S)-1-tert-butyl 2-methyl 2,4,4-trimethylpyrrolidine-1,2-dicarboxylate
Rendimiento 75.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)CC(C)(C)CN1
Reaction #2048586
(S)-Methyl 2,4,4-trimethylpyrrolidine-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)CC(C)(C)CN1c1nc(Cl)nc(Nc2cc(C3CC3)[nH]n2)n1
Reaction #2048587
Compound 106E
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C)CC(C)(C)CN1C(=O)OC(C)(C)C
Reaction #2134864
( 163E )
Rendimiento 82.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C)CC(C)(C)CN1C(=O)OC(C)(C)C
Reaction #2471710
( 163E )
Rendimiento 82.1%DOI: 10.6084/m9.figshare.5104873.v1