𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Totally Stereoselective Synthesis of 1,3-Disaccharides Through Diels—Alder Reactions.

✍ Scribed by Alessandra Bartolozzi; Stefania Pacciani; Cecilia Benvenuti; Martina Cacciarini; Francesca Liguori; Stefano Menichetti; Cristina Nativi

Publisher
John Wiley and Sons
Year
2004
Weight
201 KB
Volume
35
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Stereoselective Syn
ChemInform Abstract: Stereoselective Synthesis of 1,3-Disaccharides Through Diels—Alder Reactions. Part 2. Convenient Protecting Groups for Heterodienes and Conformational Evaluations.
✍ Gabriele Gabrielli; Fabrizio Melani; Sara Bernasconi; Carlotta Lunghi; Barbara R 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 38 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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: Total Synthesis of
ChemInform Abstract: Total Synthesis of Maturinone Through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione.
✍ O. CHERKAOUI; P. NEBOIS; H. FILLION 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 3 views

Total Synthesis of Maturinone Through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione. -Using a known directing effect of a bromine atom located on the double bond of a quinone such as (III) in a Diels-Alder reaction maturinone ( VI) is synthesized in an efficient and regiosel