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Quasi-racemic FMS

Enantiopure or enantioenriched compounds can be obtained by asymmetric synthesis or by separation of a racemic reaction mixture. Quasi-racemic FMS provides a new approach to enantiomeric compounds (see Scheme 13.2) [26, 27]. Quasi-racemic synthesis starts with two individual R- and 5-enantiomers attached to two different fluorous tags. After steps of mixture synthesis followed by F-HPLC demixing and detagging, two individual products as enantiomers are obtained (see Sections 13.2.1 and 13.2.2). The separation and identification of the final quasi-enantiomers are ensured by the phase-tag-based F-HPLC. In a more complicated quasi-racemic FMS, additional enantiomerically pure building blocks and fluorous tags can be used to generate more chiral centers and more than two products as stereoisomers (see Sections 13.2.3 to 13.2.8). [Pg.337]

Scheme 13.4 Quasi-racemic FMS of (S)- and (R)-pyridovericins. 13.2.2 Synthesis of Enantiomers of Mappicine... Scheme 13.4 Quasi-racemic FMS of (S)- and (R)-pyridovericins. 13.2.2 Synthesis of Enantiomers of Mappicine...

See other pages where Quasi-racemic FMS is mentioned: [Pg.337]    [Pg.338]    [Pg.339]    [Pg.340]    [Pg.347]    [Pg.337]    [Pg.338]    [Pg.339]    [Pg.340]    [Pg.347]   
See also in sourсe #XX -- [ Pg.337 ]




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