Synthesis and rearrangement of dispiro[2.0.3.4]-, dispiro-[3.0.3.3]- and dispiro[2.1.3.3]undecanes - preferred C4-C5 over C3-C4 and C4-C3 over C5-C6 rearrangements
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Synthesis and rearrangement of functionalized dispiro[2.1.3.3]Undecanes - preferred C4C5 over C3C4 ring enlargements
2. Evaluation of strain in hydrocarbons. The strain in adamantane and its origin
3. Preparative-Scale Syntheses of Bicyclobutylidene, Methylenecyclobutane and Cyclobutanone
4. Oxaspiropentane. A rapid route to cyclobutanone
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1. Occurrence, synthesis and applications of natural and designed [3.3.3]propellanes;Natural Product Reports;2020
2. Four-Membered Cycle Formation Challenge: GaCl3 -Promoted Formal [2+2]-Cycloaddition of Donor-Acceptor Cyclopropanes to Bicyclobutylidene;European Journal of Organic Chemistry;2019-05-16
3. Oxyfunctionalization of CH2-Group Activated by Adjacent Three-Membered Ring;Current Organic Synthesis;2018-06-12
4. Beyond the Dimer and Trimer: Tetraspiro[2.1.2 5 .1.2 9 .1.2 13 .1 3 ] hexadecane‐1,3,5,7‐tetraone—the Cyclic Tetramer of Carbonylcyclopropane;Chemistry – A European Journal;2016-02-03
5. Four-Membered Ring-Containing Spirocycles: Synthetic Strategies and Opportunities;Chemical Reviews;2014-07-08
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