Article
Publicly Available
Development of transition-metal-catalyzed cycloaddition reactions leading to polycarbocyclic systems
-
Moisés Gulías
Published/Copyright:
February 7, 2011
Online erschienen: 2011-2-7
Erschienen im Druck: 2011-2-7
© 2013 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Preface
- New methods for the synthesis of certain alkaloids and terpenoids
- Synthetic studies toward the spiroimine unit of the spirolides
- Chirospecific synthesis: Catalysis and chiral pool hand in hand
- Fumonisin: A template for methodology development and drug discovery
- 1,5-Polyols: Challenging motifs for configurational assignment and synthesis
- Improved synthesis of Bn5CpRu(CO)2Cl and its application as racemization catalyst in preparative-scale metalloenzymatic dynamic kinetic resolution of 1-phenylethanol
- Synthesis of mycalazol and mycalazal analogs with potent antiproliferating activities
- Development of transition-metal-catalyzed cycloaddition reactions leading to polycarbocyclic systems
- New samarium diiodide-induced cyclizations
- Fun with radicals: Some new perspectives for organic synthesis
- Enhancement of ruthenium-catalyzed olefin metathesis reactions: Searching for new catalyst or new reaction conditions?
- Halodiazoacetates as useful tools for selective halo-functionalization
- Rhodium-catalyzed enantioselective intermolecular hydroacylation reactions
- Specific conjugate addition to α,β-acetylenic ketones
- Enantioselective construction of new chiral cyclic scaffolds using [2 + 2 + 2] cycloaddition
- Oxidative decarboxylation of α-amino acids to nitriles using o-iodoxybenzoic acid in aqueous ammonia
- Convergent synthesis of new types of stabilized carotenoid compounds
- Multicomponent synthesis of polysubstituted γ-butyrolactones under Barbier-like conditions
- Rational design of novel ligands for environmentally benign cross-coupling reactions
- 2-Substituted agelasine analogs: Synthesis and biological activity, and structure and reactivity of synthetic intermediates
- An oxidative carbon–carbon bond-forming reaction proceeds via an isolable iminium ion
- Design of frustrated Lewis pair catalysts for metal-free and selective hydrogenation
- Nitroxides and nucleic acids: Chemistry and electron paramagnetic resonance (EPR) spectroscopy
- Chemical genetics approach to drug discovery by diversity-oriented synthesis (DOS) of peptidomimetics
- Selective transformations of cephalostatin analogues
- Efficient and green synthesis of new polycyclic procyanidin derivatives via tandem dinucleophilic addition of indolin-2-thiones to flavylium salts
- 2-Hydroxypropyl derivatives of 1,2,3-thiadiazole and 1,2,3-triazole: Synthesis and antifungal activity
- Synthesis of a rhodanine-based compound library targeting Bcl-XL and Mcl-1
Keywords for this article
alkylidenecyclopropanes;
allenes;
cycloaddition;
polycycles;
transition metals
Articles in the same Issue
- Preface
- New methods for the synthesis of certain alkaloids and terpenoids
- Synthetic studies toward the spiroimine unit of the spirolides
- Chirospecific synthesis: Catalysis and chiral pool hand in hand
- Fumonisin: A template for methodology development and drug discovery
- 1,5-Polyols: Challenging motifs for configurational assignment and synthesis
- Improved synthesis of Bn5CpRu(CO)2Cl and its application as racemization catalyst in preparative-scale metalloenzymatic dynamic kinetic resolution of 1-phenylethanol
- Synthesis of mycalazol and mycalazal analogs with potent antiproliferating activities
- Development of transition-metal-catalyzed cycloaddition reactions leading to polycarbocyclic systems
- New samarium diiodide-induced cyclizations
- Fun with radicals: Some new perspectives for organic synthesis
- Enhancement of ruthenium-catalyzed olefin metathesis reactions: Searching for new catalyst or new reaction conditions?
- Halodiazoacetates as useful tools for selective halo-functionalization
- Rhodium-catalyzed enantioselective intermolecular hydroacylation reactions
- Specific conjugate addition to α,β-acetylenic ketones
- Enantioselective construction of new chiral cyclic scaffolds using [2 + 2 + 2] cycloaddition
- Oxidative decarboxylation of α-amino acids to nitriles using o-iodoxybenzoic acid in aqueous ammonia
- Convergent synthesis of new types of stabilized carotenoid compounds
- Multicomponent synthesis of polysubstituted γ-butyrolactones under Barbier-like conditions
- Rational design of novel ligands for environmentally benign cross-coupling reactions
- 2-Substituted agelasine analogs: Synthesis and biological activity, and structure and reactivity of synthetic intermediates
- An oxidative carbon–carbon bond-forming reaction proceeds via an isolable iminium ion
- Design of frustrated Lewis pair catalysts for metal-free and selective hydrogenation
- Nitroxides and nucleic acids: Chemistry and electron paramagnetic resonance (EPR) spectroscopy
- Chemical genetics approach to drug discovery by diversity-oriented synthesis (DOS) of peptidomimetics
- Selective transformations of cephalostatin analogues
- Efficient and green synthesis of new polycyclic procyanidin derivatives via tandem dinucleophilic addition of indolin-2-thiones to flavylium salts
- 2-Hydroxypropyl derivatives of 1,2,3-thiadiazole and 1,2,3-triazole: Synthesis and antifungal activity
- Synthesis of a rhodanine-based compound library targeting Bcl-XL and Mcl-1