This method uses chiral starting materials obtained from natural sources. For example, amino acids, sugars, or other naturally occurring chiral compounds can be transformed into diamines while maintaining their enantiopurity.
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(2S,3S)-2-(1-methylethyl)-4-nitro-3-phenylbutyraldehyde
C29H41NO3
Glycine, N-[(4-nitrophenyl)sulfonyl]-N-2-propenyl-, ethyl ester
8-phenylmethoxycarbonylamino-8-(2'-propenyl)-1,4-dioxaspiro[4.5]decane
tert-butyldiphenyl(((4R,5R)-2,2,5-trimethyl-1,3-dioxan-4-yl)methoxy)silane
C43H71NO10Si
