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• W2007993742 abstract "The Garner aldehyde-derived methylene alkene 5 and the corresponding benzyloxycarbonyl compound 25 undergo hydroboration with 9-BBN-H followed by palladium-catalyzed Suzuki coupling reactions with aryl and vinyl halides. After one-pot hydrolysis-oxidation, a range of known and novel nonproteinogenic amino acids were isolated as their N-protected derivatives. These novel organoborane homoalanine anion equivalents are generated and transformed under mild conditions and with wide functional group tolerance: electron-rich and -poor aromatic iodides and bromides (and a vinyl bromide) all undergo efficient Suzuki coupling. The extension of this methodology to prepare meso-DAP, R,R-DAP, and R,R-DAS is also described." @default.
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• W2007993742 date "2002-02-20" @default.
• W2007993742 modified "2023-10-12" @default.
• W2007993742 title "Enantiomerically Pure α-Amino Acid Synthesis via Hydroboration−Suzuki Cross-Coupling" @default.
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• W2007993742 doi "https://doi.org/10.1021/jo010865a" @default.
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