𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A De Novo Approach to the Synthesis of Glycosylated Methymycin Analogues with Structural and Stereochemical Diversity

✍ Scribed by Borisova, Svetlana A.; Guppi, Sanjeeva R.; Kim, Hak Joong; Wu, Bulan; Penn, John H.; Liu, Hung-wen; O’Doherty, George A.

Book ID
126592705
Publisher
American Chemical Society
Year
2010
Tongue
English
Weight
531 KB
Volume
12
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A new and efficient approach to the synt
A new and efficient approach to the synthesis of nicotine and anabasine analogues
✍ Kun Huang; Margarita Ortiz-Marciales; Melvin De Jesús; Viatcheslav Stepanenko 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 114 KB

## Abstract magnified image A straightforward and practical approach was established for the synthesis of nicotine and anabasine analogues by the cyclization of mesylated 1‐(3‐pyridinyl)‐1,4, and 1,5‐diol derivatives to form the pyrrolidino or piperidino fragments. Nicotine analogue (__S__)‐**15**

ChemInform Abstract: A New Approach to P
ChemInform Abstract: A New Approach to Pyranofuranones, Advanced Intermediates for the Synthesis of Manoalide, Cacospongionolides and Their Analogues.
✍ A. SORIENTE; M. DE ROSA; A. SCETTRI; G. SODANO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

A New Approach to Pyranofuranones, Advanced Intermediates for the Synthesis of Manoalide, Cacospongionolides and Their Analogues. -A simple and convergent approach for the synthesis of the pyranofuranone fragment of the marine sesterterpenes manoalide (cf. ( IX)) and cacospongionolides (cf. (XI)) s