𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: A New Synthesis of 1β-Alkylcarbapenems Utilizing Eschenmoser Sulfide Contraction of the Novel Thiazinone Intermediates.

✍ Scribed by O. SAKURAI; T. OGIKU; M. TAKAHASHI; M. HAYASHI; T. YAMANAKA; H. HORIKAWA; T. IWASAKI

Publisher
John Wiley and Sons
Year
2010
Weight
36 KB
Volume
28
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A New Diastereosele
ChemInform Abstract: A New Diastereoselective Synthesis of a 1β-Methylcarbapenem Intermediate.
✍ Chang-Young Oh; Won-Hun Ham 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Synthesis and NMR S
ChemInform Abstract: Synthesis and NMR Studies of Key Intermediates to a New Class of β -Lactam: The Trinems.
✍ C. MARCHIORO; G. PENTASSUGLIA; A. PERBONI; D. DONATI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Synthesis and NMR Studies of Key Intermediates to a New Class of β -Lactam: The Trinems. -All 4 isomeric epoxides (X), (XI), (XIV), and (XV), which are key intermediates for trinems, a new family of antibiotics, are synthesized starting from the azetidinone (I). -(MARCHIORO, C.;