Abstract
The 1β-methylcarbapenem antibiotics represented by 3, 4, and 5, have been the focus of current synthetic endeavor due to prominent antibacterial activities and broad spectra as well as enhanced chemical and metabolic stability. Progress of the syntheses of 1β-methylcarbapenem key intermediates represented by 6, are reviewed based on the synthetic methods of the characteristic 1β-methyl substituent involved in the contiguous four chiral centers of 6. © 1989, The Society of Synthetic Organic Chemistry, Japan. All rights reserved.
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CITATION STYLE
Ito, Y., & Terashima, S. (1989). Synthesis of the 1β-Methylcarbapenem Key Intermediates. Journal of Synthetic Organic Chemistry, Japan, 47(7), 606–618. https://doi.org/10.5059/yukigoseikyokaishi.47.606
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