A novel stereoselective route to (S)-(+)-α-(fluromethyl)histidine : α-halomethylation of (2R,4S)-3-benzoyl-2-(1,1-dimethylethyl)-1-methyl-4-[(N-tritylimidazol-4'-yl)methyl]-1,3-imidazolidin-5-one. Synthesis and 1H NMR spectroscopy
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Veröffentlicht in: | Journal of organic chemistry 1993, Vol.58 (3), p.709-713 |
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container_title | Journal of organic chemistry |
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creator | GROZINGER, K. G KRIWACKI, R. W LEONARD, S. F PITNER, T. P |
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Synthesis and 1H NMR spectroscopy</title><source>ACS Publications</source><creator>GROZINGER, K. G ; KRIWACKI, R. W ; LEONARD, S. F ; PITNER, T. P</creator><creatorcontrib>GROZINGER, K. G ; KRIWACKI, R. W ; LEONARD, S. F ; PITNER, T. 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source | ACS Publications |
subjects | Chemistry Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings Organic chemistry Preparations and properties |
title | A novel stereoselective route to (S)-(+)-α-(fluromethyl)histidine : α-halomethylation of (2R,4S)-3-benzoyl-2-(1,1-dimethylethyl)-1-methyl-4-[(N-tritylimidazol-4'-yl)methyl]-1,3-imidazolidin-5-one. Synthesis and 1H NMR spectroscopy |
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