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Total Synthesis of the Marine Alkaloids (−)-Lepadins A, B, and C Based on Stereocontrolled Intramolecular Acylnitroso-Diels−Alder Reaction

✍ Scribed by Ozawa, Tetsuji; Aoyagi, Sakae; Kibayashi, Chihiro

Book ID
120655154
Publisher
American Chemical Society
Year
2001
Tongue
English
Weight
156 KB
Volume
66
Category
Article
ISSN
0022-3263

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ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of the Marine Alkaloids (-)-Lepadins A (X), B (IX), and C (XI) Based on Stereocontrolled Intramolecular Acylnitroso-Diels—Alder Reaction.
✍ Tetsuji Ozawa; Sakae Aoyagi; Chihiro Kibayashi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 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

Diastereoselective intramolecular diels-
Diastereoselective intramolecular diels-alder reaction of N-alkoxycarbonyl -1-aza-1,3-butadienes and a total synthesis of the piperidine alkaloid, (±)-sedridine.
✍ Tadao Uyehara; Naoki Chiba; Ichiro Suzuki; Yoshinori Yamamoto 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 264 KB

## Total synthesis of C-t)-sedridine, the piperidine alkaloid, was accomplished on the basis of diastereoselecthe intramolecvlarDieh4lderiels-Alderreactign oftbe J,d-unsahmted N-alkoxycahnyl-l-aza-1,3-butaohe genemtedin situ tivm N&imetiyL6iyI-I-aza-but&ens and the cMomtiite of +mten-24.