Synthesis and reactions of hydroxyspiro[5.2]cyclooctenones based on the cyclization of the dianions of acetone and diethyl 2-oxopropylphosphonate with 1,1-diacylcyclopropanes-Reference-Cited by-同舟云学术

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Synthesis and reactions of hydroxyspiro[5.2]cyclooctenones based on the cyclization of the dianions of acetone and diethyl 2-oxopropylphosphonate with 1,1-diacylcyclopropanes

Published:2008-03 Issue:14 Volume:49 Page:2254-2257
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Rasool Nasir,Rashid Muhammad A.,Adeel Muhammad,Görls Helmar,Langer Peter

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference42 articles.

1. Isolation of Lampterol, an Antitumour Substance from Lampteromyces japonicus

2. Antibiotic Substances from Basidiomycetes: VII. Clitocybe Illudens

3. The Structures of the Basidiomycete Metabolites Illudin S and Illudin M

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1. Adventures in the Chemistry of 1,1-Diacylcyclopropanes;Synlett;2023-03-21

2. A novel spirocyclic scaffold accessed via tandem Claisen rearrangement/intramolecular oxa-Michael addition;Beilstein Journal of Organic Chemistry;2022-12-06

3. Synthesis of Activated Cyclopropanes by MHIRC Strategy: A Facile and Efficient Approach to Spirocyclopropanes Using N-Halosulfonamides;Synthesis;2016-06-20

4. An efficient organocatalytic enantioselective synthesis of spironitrocyclopropanes;Org. Biomol. Chem.;2013

5. Carbanions and Electrophilic Aliphatic Substitution;Organic Reaction Mechanisms · 2008;2011-08-05

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