Revised Structures for the Lactones Obtained by Reduction of the Adduct of Ergosterol Acetate with Maleic Anhydride
Author:
Affiliation:
1. Department of Medical Chemistry and Biochemistry, University of Milan, Via Saldini 50, 20133-Milan, Italy.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo970710w
Reference15 articles.
1. Synthesis of (2R,3S,22R,23R)- and (2R,3S,22S,23S)-2,3,22,23-tetrahydroxy-B-homo-8-oxa-5.alpha.-ergostan-7-ones, two new brassinolide analogs
2. Highly Stereocontrolled Formal Synthesis of Brassinolide via Chiral Sulfoxide-Directed SN2‘ Reactions
3. ACS Symposium Series 474;Brassinosteroids
4. Brassinolide, a plant growth-promoting steroid isolated from Brassica napus pollen
5. Über Ergosterylacetat-maleinsäureanhydrid und seine Hydro-derivate
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1. Diversity-Oriented Synthesis of Enantiomerically Pure Steroidal Tetracycles Employing Stille/Diels-Alder Reaction Sequences;Chemistry - A European Journal;2008-08-18
2. Synthesis of 5α,8α-ethanoergosta-2,6,22-triene-2′β-hydroxymethylene-1′β-carboxylic acid lactone, a key intermediate for the synthesis of a brassinolide analogue;Chemistry and Physics of Lipids;1999-12
3. Synthesis of two analogues of brassinolide, possible plant growth promoting steroids;Tetrahedron;1999-03
4. Steroids: reactions and partial synthesis;Natural Product Reports;1999
5. Regio- and Stereoselectivity in Metal Hydride Reduction of the Diels−Alder Adduct of Ergosteryl Acetate and Maleic Anhydride;The Journal of Organic Chemistry;1998-02-18
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