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Type 2 Intramolecular N-Acylnitroso Diels−Alder Reaction: Stereoselective Synthesis of Bridged Bicyclic Oxazinolactams

✍ Scribed by Chow, Chun P.; Shea, Kenneth J.; Sparks, Steven M.

Book ID
115472054
Publisher
American Chemical Society
Year
2002
Tongue
English
Weight
59 KB
Volume
4
Category
Article
ISSN
1523-7060

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📜 SIMILAR VOLUMES

ChemInform Abstract: Type 2 Intramolecul
ChemInform Abstract: Type 2 Intramolecular Nitroso Diels—Alder Reaction. Synthesis and Structure of Bridgehead Oxazinolactams.
✍ Steven M. Sparks; Jesse D. Vargas; Kenneth J. Shea 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 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

Type 2 Intramolecular N -Acylnitroso Die
Type 2 Intramolecular N -Acylnitroso Diels−Alder Reaction: Scope and Application to the Synthesis of Medium Ring Lactams
✍ Sparks, Steven M.; Chow, Chun P.; Zhu, Liang; Shea, Kenneth J. 📂 Article 📅 2004 🏛 American Chemical Society 🌐 English ⚖ 303 KB

Heteroatom variants of the type 2 intramolecular Diels-Alder reaction provide an efficient method for the preparation of bridged bicyclic heterocycles. The type 2 variant of the intramolecular N-acylnitroso Diels-Alder reaction is an effective method for the synthesis of bridged bicyclic oxazinolact