Diastereofacial selectivity in Diels–Alder reactions of buta-1,3-dienes having stereogenic allylic heteroatom substituents at the C-2 position
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1992/C3/C39920000953
Reference17 articles.
1. Preparation of racemic and chiral alkyl(1,3-butadien-2-yl)methanol derivatives utilizing 1-trimethylsilyl-2,3-butadiene as a diene source
2. Enantio- and stereocontrolled syntheses of branched-chain sugar, L-arcanose and L-olivomycose based on the chemistry of 1-trimethylsilyl-2,3-butadiene
3. Concise enantioselective synthesis of a key synthetic intermediate for anticancer anthracyclines based on the chemistry of 1-trimethylsilylbuta-2,3-diene
4. Heteroatom-directed .pi.-facial diastereoselection in Diels-Alder cycloadditions of plane-nonsymmetric cyclopentadienes
5. Diels-Alder reactions of dieno-pyranosides. Anomeric versus allylic stereoselection
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