A new strategy for the synthesis of spiro[4,5]decanes: A formal total synthesis of acorone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Novel cyclization by stannyl anion generated from (trimethylsilyl)tributylstannane (Me3SiSnBu3) and fluoride ion. Application to natural product synthesis
2. A simple strategy for spirocyclopentannulation of cyclic ketones. Formal total synthesis of (±)-acorone
3. Synthesis based on cyclohexadienes. Part 21.1 Total synthesis of (±)-hinesol and (±)-10-epi-hinesol
4. Synthesis based on cyclohexadienes. Part 24.1 A new total synthesis of pupukean-2-one and a facile entry to copa and ylanga type sesquiterpene skeletons
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1. Synthetic Approach toward (–)-Tetrodotoxin via Construction of the Bicyclo[2.2.2]octane Skeleton;Synlett;2022-01-28
2. Syntheses and Applications of Functionalized Bicyclo[3.2.1]octanes: Thirteen Years of Progress;Chemical Reviews;2012-10-19
3. ChemInform Abstract: A New Strategy for the Synthesis of Spiro[4,5]decanes: A Formal Total Synthesis of Acorone.;ChemInform;2010-06-15
4. Synthetic studies towards the nor-triterpene pfaffic acid: Synthesis of DEF ring fragment via tandem radical cyclization rearrangement reactions;Arkivoc;2004-08-04
5. Synthesis based on cyclohexadienes Part 36: an efficient methodology for the construction of spiro[4.5]decanes: a formal synthesis of acorone;Arkivoc;2003-02-27
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