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Oxazaborolidine-Derived Lewis Acid Assisted Lewis Acid as a Moisture-Tolerant Catalyst for Enantioselective Diels—Alder Reactions.

✍ Scribed by Kentaro Futatsugi; Hisashi Yamamoto

Publisher
John Wiley and Sons
Year
2005
Weight
25 KB
Volume
36
Category
Article
ISSN
0931-7597

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📜 SIMILAR VOLUMES

Oxazaborolidine-Derived Lewis Acid Assis
Oxazaborolidine-Derived Lewis Acid Assisted Lewis Acid as a Moisture-Tolerant Catalyst for Enantioselective Diels–Alder Reactions
✍ Kentaro Futatsugi; Hisashi Yamamoto 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 155 KB 👁 2 views

The Diels-Alder reaction is one of the most powerful construction processes in organic synthesis, especially for the formation of molecules containing quaternary carbon stereocenters. [1] For this reason there has been much research on the development of enantioselective versions using chiral Lewis

Oxazaborolidine-Derived Lewis Acid Assis
Oxazaborolidine-Derived Lewis Acid Assisted Lewis Acid as a Moisture-Tolerant Catalyst for Enantioselective Diels–Alder Reactions
✍ Kentaro Futatsugi; Hisashi Yamamoto 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 155 KB 👁 1 views

The Diels-Alder reaction is one of the most powerful construction processes in organic synthesis, especially for the formation of molecules containing quaternary carbon stereocenters. [1] For this reason there has been much research on the development of enantioselective versions using chiral Lewis