Synthesis of Aristotelia-Type Alkaloids. Part XII. Total synthesis of (−)-tasmanine. Stereoelectronic factors that control the rearrangement of 3H-indol-3-ol derivatives to oxindoles ( = 1,3-dihydro-2H-indol-2-ones) or to pseudoindoxyls ( =1,2-dihydro-3H--Reference-Cited by-同舟云学术

Synthesis of Aristotelia-Type Alkaloids. Part XII. Total synthesis of (−)-tasmanine. Stereoelectronic factors that control the rearrangement of 3H-indol-3-ol derivatives to oxindoles ( = 1,3-dihydro-2H-indol-2-ones) or to pseudoindoxyls ( =1,2-dihydro-3H-

Published:1993-08-11 Issue:5 Volume:76 Page:1847-1862
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Güller Rolf,Borschberg Hans-Jürg

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference56 articles.

1. Synthesis of Aristotelia-type alkaloids. Part XI. Total syntheses of (+)-sorelline and (+)-aristolasene

2. Tasmanin, ein neues Indolalkaloid ausAristotelia peduncularis(LABILL.) HOOK. F. 181. Mitteilung über organische Naturstoffe

3. Aristoserratenine and tasmanine: structures and absolute configurations

4. Nouveaux alcaloides indoliques derives de l'aristoteline extraits d'aristotelia australasica

5. Aristotelinone and serratoline: New indole alkaloids from Aristotelia serrata W.R.B. Oliver

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