The key step in this transformation is to convert the (1S,3S)-cis-1,3-disubstituted tetrahydro-β-carbolines into the (1S,3R)-trans-1,3-disubstituted tetrahydro-β-carbolines while maintaining the stereochemistry. The choice of reagents and reaction conditions is critical to achieve the desired stereochemistry. This transformation may involve the use of chiral catalysts or reagents to control the stereochemistry of the reaction.
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(1S,3S)-methyl 1-(4-fluorophenyl)-2-(naphthalen-1-ylmethyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate
N-((1S,2R,3R,4S,5R,6R)-3-Amino-2,4,5,6-tetrahydroxy-cyclohexyl)-acetamide
4-<3β-<(6-deoxy-α-L-mannopyranosyl)oxy>-14β-hydroxyandrost-4-en-17β-yl>-1,2-benzenedimethanol
DL-Limonene
