PDF herunterladen
Synlett 1995; 1995(6): 663-665
DOI: 10.1055/s-1995-5035
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Stereoselective Approach to Tetrahydropyran by Iodoetherifications of (2S,3S)-2,3-Bis(t-butyldimethylsilyloxy)-5-alkene-1-ol

Tatsuya Minami, Akio Moriyama, Miyoji Hanaoka*
  • *Faculty of Pharmaceutical Sciences, Kanazawa University, 13-1 Takara-machi, Kanazawa 920, Japan
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
31. Dezember 2000 (online)

  als PDF herunterladen  Lizenzen und Reprints Alle Artikel dieser Rubrik

Iodoetherification of 2,3-bis(t-butyldimethylsilyloxy)-5-alkene-1-ol gave tetrahydropyrans in good to excellent diastereoselectivity, which was conformationally controlled by introduction of protected vicinal (S,S)-diol functional group.

Iodoetherification - 5-Alkene-1-ol - Diastereoselective tetrahydropyran formation - Protected vicinal (S,S)-diol - Conformational control