Regio- and Stereoselectivity in Metal Hydride Reduction of the Diels−Alder Adduct of Ergosteryl Acetate and Maleic Anhydride
Author:
Affiliation:
1. Department of Chemistry, University of Auckland, Private Bag 92019, Auckland, New Zealand
2. Department of Chemistry, Northeastern University, Boston, Massachusetts 02115-5096
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo971923o
Reference8 articles.
1. Steroidal adducts. II. Stereoselectivity in .gamma.-lactone synthesis from a steroidal cyclic anhydride
2. Steroidal adducts. IV. Variable selectivity in hydride reductions of a steroidal cyclic anhydride
3. Über Ergosterylacetat-maleinsäureanhydrid und seine Hydro-derivate
4. Revised Structures for the Lactones Obtained by Reduction of the Adduct of Ergosterol Acetate with Maleic Anhydride
5. The regioselectivity of metal hydride reductions of 3-substituted phthalic anhydrides
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1. 8.10 Reduction of Carboxylic Acids and their Derivatives to Alcohols, Ethers, and Amines;Comprehensive Organic Synthesis II;2014
2. Diversity-Oriented Synthesis of Enantiomerically Pure Steroidal Tetracycles Employing Stille/Diels-Alder Reaction Sequences;Chemistry - A European Journal;2008-08-18
3. Stille/Diels−Alder Reaction Sequences: Diversity-Oriented Access to Novel Steroids;Organic Letters;2007-01-12
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5. Maleic Anhydride, Maleic Acid, and Fumaric Acid;Kirk-Othmer Encyclopedia of Chemical Technology;2001-10-18
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