Enantioselective, Electrocatalytic Lactonization of Methyl-substituted Diols on a TEMPO-modified Graphite Felt Electrode in the Presence of (−)-Sparteine-Reference-Cited by-同舟云学术

Enantioselective, Electrocatalytic Lactonization of Methyl-substituted Diols on a TEMPO-modified Graphite Felt Electrode in the Presence of (−)-Sparteine

Published:1996-12 Issue:12 Volume:25 Page:1043-1044
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Yanagisawa Yoshinori,Kashiwagi Yoshitomo,Kurashima Futoshi,Anzai Jun-ichi,Osa Tetsuo,Bobbitt James M.

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/25/12/25_12_1043/_pdf

Reference14 articles.

1. Totalsynthese von nat�rlichem ?-Tocopherol. 2. Mitteilung. Aufbau der Seitenkette aus (?)-(S)-3-Methyl-?-butyrolacton

2. Synthesis of mammalian dolichols from plant polyprenols

3. 3-Methyl-.gamma.-butyrolactones as templates for the synthesis of polypropionates: the basic strategy

4. Applications of the 3-methyl-.gamma.-butyrolactone strategy to the synthesis of polypropionates: the Prelog-Djerassi lactonic ester, ent-invictolide, and the C19-C27 fragment of rifamycin S

5. Formal synthesis of (-)-calcimycin (A-23187) via the 3-methyl-.gamma.-butyrolactone approach

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