A Double Iodoetherification of ?-Symmetric Diene Acetals for Installing Four Stereogenic Centers in a Single Operation: Short Asymmetric Total Synthesis of Rubrenolide-Reference-Cited by-同舟云学术

A Double Iodoetherification of ?-Symmetric Diene Acetals for Installing Four Stereogenic Centers in a Single Operation: Short Asymmetric Total Synthesis of Rubrenolide

Published:2005-01-21 Issue:5 Volume:44 Page:734-737
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Fujioka Hiromichi,Ohba Yusuke,Hirose Hideki,Murai Kenichi,Kita Yasuyuki

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference22 articles.

1. Asymmetric Induction via an Intramolecular Haloetherification Reaction of Chiral Ene Acetals: A Novel Approach to Optically Active 1,4- and 1,5-Diols

2. Remote asymmetric induction for chiral 1,4-diols using a chiral acetal derived from chiral hydrobenzoin

3. Chiral Route to Some Alkaloids through Asymmetric Iodolactonization

4. Enantioselective halolactonisation of bis-γ,δ-unsaturated carboxylic acid derivatives: use of a sultam and oxazolidine-2-ones as chiral auxiliary

5. Highly enantioselective creation of quaternary carbons in a halolactonization of bis-γ,δ-unsaturated carboxylic imides derived from a camphorsultam: Enantioselective synthesis of (+)-mesembrine

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