NDLI: Endogenous alkaloids in man. 28. (1R, 3S))-1-trichloromethyl-1,2,3,4-tetrahydro-β-carboline-3-carboxamide methanol solvate, a potential synthetic precursor to enantiomerically pure TaClo

Content Provider	Semantic Scholar
Author	Peters, Karl Peters, E. Kirsten Blank, Michael Protzen, J.-A. Feineis, Doris God, Ralf Bringmann, Gerhard
Copyright Year	1998
Abstract	The title compound, C13H12Cl3N3O.CH3OH, was prepared by amidolysis of the corresponding methyl tetrahydro-β-carboline-3-carboxylate, obtained in turn by condensation of tryptophan methyl ester and chloral. The crystal structure confirms the relative cis-array of the substituents at C1 and C3, and thus the absolute R configuration at C1.
Starting Page	1005
Ending Page	1007
Page Count	3
File Format	PDF HTM / HTML
DOI	10.1107/S0108270198001437
Volume Number	54
Alternate Webpage(s)	https://journals.iucr.org/c/issues/1998/07/00/jz1190/jz1190.pdf
Alternate Webpage(s)	https://doi.org/10.1107/S0108270198001437
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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