𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthetic Strategy toward the C44–C65 Fragment of Mirabalin

✍ Scribed by Echeverria, Pierre-Georges; Prévost, Sébastien; Cornil, Johan; Férard, Charlène; Reymond, Sébastien; Guérinot, Amandine; Cossy, Janine; Ratovelomanana-Vidal, Virginie; Phansavath, Phannarath


Book ID
123613089
Publisher
American Chemical Society
Year
2014
Tongue
English
Weight
705 KB
Volume
16
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthetic studies on spongistatins: synt
✍ Mohammad Samadi; Christian Munoz-Letelier; Stéphane Poigny; Michèle Guyot 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 173 KB

A convergent synthesis of the C29-C44 fragment, the common subunit of the spongipyran macrolides is described. The key step of the synthesis is the C-glycosidation reaction which is based on coupling of the lithiated F-ring sulfone with the E-ring aldehyde, and subsequent reductive desulfonylation t

ChemInform Abstract: Synthetic Studies o
✍ Mohammad Samadi; Christian Munoz-Letelier; Stephane Poigny; Michele Guyot 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 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: Synthetic Approache
✍ A. SHIMIZU; S. NISHIYAMA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Synthetic Approaches Towards Laulimalide: Synthesis of the C 12 -C 29 Fragment. -The synthesis of the title compound, i.e. the C 12 -C 29 fragment (VI), is based on a trans Julia olefination of the aldehyde (II) and the sulfone (IV) as key step. -(SHIMIZU, A.;