The stereoselective synthesis of two precursors of tricyclic Ξ²-ring-forming reaction followed by the reduction of a functionalized aromatic substituent at C-4 of the Ξ²-lactam lactam antibiotics (trinems) has been attempted by a novel approach that involves a highly stereoselective azetidinone nucleu
β¦ LIBER β¦
Novel approach to the synthesis of sugar sulfones via trans-sulfonylation of a unique heteroaryl precursor
β Scribed by C. Lorin; C. Marot; V. Gardon; P. Rollin
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 103 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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