The isolated diastereomer can be used as a key intermediate for the synthesis of (+)-blastmycinone through further chemical transformations. These may include functional group manipulations, protecting group strategies, and other reactions to build the molecular structure of the target compound.
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(3R,4S)-4-Benzyloxy-3-hydroxy-pentanoic acid tert-butyl ester
(3E,5E)-6-chloro-1-(p-methoxyphenyl)hexa-3,5-diene
((3S,4R)-3-tert-Butoxycarbonylamino-2-oxo-4-phenethyl-azetidin-1-yl)-acetic acid methyl ester
benzyl 7-oxo-1-azabicyclo[3.2.0] hept-2-ene-2-carboxylate
3-(3-carboxy-4-phenyl-butyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
C15H20O3
(4S,2S)-4-Chloro-<2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxo-3-<2-oxo-4-(phenylmethyl)-3-oxazolidinyl>propyl>benzene
(+/-)-(3aα,4α,6aα)-1,3-dibenzyl-3a,4,6,6a-tetrahydro-4-hydroxy-1H-thieno<3,4-d>imidazol-2(3H)-one
2H-Pyran, 2-(3-butenyl)-6-(1,1-dimethylethoxy)tetrahydro-3-(phenylmethoxy)-, (2R,3S,6R)-
(1R,2R,5R)-2-phenylsulfonyl-6,8-dioxabicyclo[3.2.1]octan-3-one
PhSH
MeI
