Lewis acid-promoted tandem desulfurization and hydroxylation of γ-phenylthio-substituted lactams: novel synthetic strategy of isoindolobenzazepine alkaloid, chilenine-Reference-Cited by-同舟云学术

Lewis acid-promoted tandem desulfurization and hydroxylation of γ-phenylthio-substituted lactams: novel synthetic strategy of isoindolobenzazepine alkaloid, chilenine

Published:2003-12 Issue:50 Volume:44 Page:9057-9060
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Yoda Hidemi,Inoue Kei-ichi,Ujihara Yasuaki,Mase Nobuyuki,Takabe Kunihiko

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

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2. (b) Ostendorf, M.; Van der Neut, S.; Rutjes, F. P. J. T.; Hiemstra, H. Eur. J. Org. Chem. 2000, 105–113;

3. (c) Hunter, R.; Richards, P. Tetrahedron Lett. 2000, 41, 3755–3758;

4. (d) Huang, P. Q.; Tang, X.; Chen, A. Q. Synth. Commun. 2000, 30, 2259–2268;

5. (e) Luzzio, F. A.; Zacherl, D.-A. P. Tetrahedron Lett. 1998, 39, 2285–2288;

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