Synthesis of functionalized bicyclo[3.2.1]octan-6-ones for diterpenoids: allylsilane directed Pummerer reaction: insertion reactions of diazoketones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Crystal and molecular structures of a natural equimolecular mixture of two epimeric diterpenes
2. Olefinic Cyclisations Initiated by Pummerer Rearrangement Products; Synthesis of Cyclic Ketones
3. Application of a three-carbon ring expansion process to bridged bicyclic systems
4. Experimental Evidence for Negative Hyperconjugation as a Component of the Polar Effect: Variation of the Ease of α-Sulfonyl Carbanion Formation with the Orientation of a β-Alkoxy Substituent
5. Synthesis of a C22-34 Subunit of the Immunosuppressant FK-506
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1. 4.4.40.72 Allylsilanes (Update 2020);SOS Knowledge Updates 2020/1;2020
2. Copper-catalyzed Pummerer type reaction of α -thio aryl/heteroarylacetates: Synthesis of aryl/heteroaryl α -keto esters;Tetrahedron Letters;2017-05
3. Transition-Metal-Catalyzed Synthesis of Spirolactones;Synthesis;2017-04-18
4. The synthesis of functionalized bridged polycycles via C–H bond insertion;Beilstein Journal of Organic Chemistry;2016-05-17
5. Syntheses and Applications of Functionalized Bicyclo[3.2.1]octanes: Thirteen Years of Progress;Chemical Reviews;2012-10-19
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