Anomalous behaviour of Rh(II)-generated carbonyl ylides: entry into functionalized spiro dioxa-bridged polycyclic frameworks
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference41 articles.
1. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds. From Cyclopropanes to Ylides;Doyle,1998
2. Cascade Processes of Metallo Carbenoids
3. Tandem processes of metallo carbenoids for the synthesis of azapolycycles
4. Facile Construction of Novel Polycyclic Ring Systems Using a Metallocarbenoid-Induced Cyclization of Acetylenic Diazo Carbonyl Compounds
5. Tandem cyclization-cycloaddition reaction of rhodium carbenoids. Scope and mechanistic details of the process
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1. Substituent-dependent generation of tricyclic frameworks by the rhodium-catalyzed cycloisomerization of homopropargyl allene-alkynes: a theoretical study;Dalton Transactions;2020
2. Synthesis of Conformationally Restricted Symmetric Macrodiolides via Carbonyl Ylides;Synthesis;2013-05-29
3. Cycloadditions of Carbonyl Ylides Derived from Diazocarbonyl Compounds;Organic Reactions;2012-05-15
4. ChemInform Abstract: Anomalous Behavior of Rh(II)-Generated Carbonyl Ylides: Entry into Functionalized Spiro Dioxa-Bridged Polycyclic Frameworks.;ChemInform;2010-05-20
5. The rhodium(II) carbenoid cyclization–cycloaddition cascade of α-diazo dihydroindolinones for the synthesis of novel azapolycyclic ring systems;Tetrahedron;2008-02
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