Article
Publicly Available
Intramolecular bis-silylation of alkenes catalyzed by palladium(0)-tert-alkyl isocyanide complex. Stereoselective synthesis of polyols
-
Y. Ito
Published/Copyright:
January 1, 2009
Published Online: 2009-01-01
Published in Print: 1996-01-01
© 2013 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Models for non-heme oxidation enzymes
- Intramolecular bis-silylation of alkenes catalyzed by palladium(0)-tert-alkyl isocyanide complex. Stereoselective synthesis of polyols
- Lewis acid complexed azacarbanions: Novel reactive intermediates of wide synthetic utility
- The development of more efficient syntheses of polycyclic diterpenes through intramolecular cyclopropanation of aryl rings in diazomethyl ketones
- Catalytic asymmetric carbon-carbon bond-forming reaction utilizing rare earth metal complexes
- Chiral animals: Powerful auxiliaries in asymmetric synthesis
- Recent developments in palladium-catalyzed oxidations
- Cyclopropyl compounds as chemical building blocks: Total syntheses of the alkaloids (-)-colchicine, imerubrine and grandirubrine
- Selective organic synthesis via group 6 metal carbene complexes
- The Birch reduction in organic synthesis
- A general method for the synthesis of bridged indole alkaloids
- Diastereoselective reactions of enolates
- Studies directed towards the development of cyclic peptide-based analogs of macrolide immunosuppressants
- Recent advances in the development of highly enantioselective synthetic methods
- Synthesis of natural g-lactones and a dilactone pyrrolizidine alkaloid via the reactions of 2-propenyl-1,3-dithiane
- Open chain 1,3-stereocontrol
- Carbohydrate building blocks in heterocyclic chemistry. Synthetic studies directed towards the herbicidins
- New asymmetric synthesis of β-hydroxy α-amino acids and analogues. Components of biologically active cyclopeptides
- Synthesis of cyclopentanoids - a never ending challenge
- Synthesis of the 'enediyne' antibiotic esperamicin-A1, and novel analogues for tumor targeting
- Search for antibody catalysts for the ene reaction
- Novel synthetic strategy for HMG-CoA reductase inhibitors
- Heteroatom-directed lithiations of chiral alkyl carbamates: A powerful tool for enantioselective synthesis
- Cobalt(II) Schiff base catalyzed biomimetic oxidation of organic substrates with dioxygen
- Radical cyclizations involving the evolution of nitrogen
- Hypervalent iodine reagents in organic synthesis: Nucleophilic substitution of p-substituted phenol ethers
- Oxacycle synthesis via radical cyclization of β-alkoxyacrylates
- Regioselective C-O bond cleavage reactions of acetals
- Asymmetric calysis of carbonyl-ene reactions and related carbon-carbon bond forming reactions
- Asymmetric synthesis of α,α-disubstituted α-amino acids
- Design of [1,n]-ambiphiles based on zincate carbenoid chemistry
- Design of a photosystem to harvest visible-light into electrons: Photosensitised one electron redox reactions in organic synthesis
- Synthetic studies on manzamine A
- Syntheses of chiral amino alcohols and diols
- Organotitanium compounds in organic synthesis
- Design and synthesis of self-assembling peptides
- Photocyclization-fragmentation route to di- and triquinanes: Stereocontrolled asymmetric synthesis of (-)-isocomene
- Regio- and stereoselective metal-mediated synthesis of polyfunctionalized alkenes
- The Michael-Aldol condensation approach to the construction of key intermediates in the synthesis of terpenoid natural products
- α-Carbonyl radicals for total synthesis of natural products
- Recent advances in asymmetric synthesis using chiral lithium amide bases
- New applications of chiral N-acyliminium precursors
- Synthetic approaches to homogynolides A and B
- Synthesis and cytotoxicity of natural (-)-quinocarcin and its related compounds
- Aspects of remote asymmetric induction using allylstannanes
- Diastereofacial control in the radical addition to chiral α-sulfinyl enones
- Towards the asymmetric synthesis of bryostatin 1
- 'Naked sugars of the second generation': Asymmetric synthesis of long-chain polypropionates and analogues starting with acetone
- Regiospecific synthesis of 3,4-disubstituted furans
- Stereoselective synthesis of acyclic natural products containing chiral vicinal diol
- Aziridine and azirine carboxylic esters
- Novel reaction products from simple organic reactions: Delineation of reaction pathways
- Synthesis of substituted imidazoles and uracils as herbicides
- Microbial metabolites - an infinite source of novel chemistry
- Preparative and mechanistic aspects of inter-estification reactions on diols and peracetylated polyphenolic compounds catalysed by lipases
- Metalloporphyrins as chemical mimics of cytochrome P-450 systems
- Molecular recognition and signalling
- Efficient syntheses of regioisomers of tiagabine
- Synthesis and spectral studies of natural chlorins having antioxidative activity
- The synthesis of taxoids from glucose
- Use of 1-menthyl ester as chiral auxiliary in the synthesis of useful chiral synthons
Articles in the same Issue
- Models for non-heme oxidation enzymes
- Intramolecular bis-silylation of alkenes catalyzed by palladium(0)-tert-alkyl isocyanide complex. Stereoselective synthesis of polyols
- Lewis acid complexed azacarbanions: Novel reactive intermediates of wide synthetic utility
- The development of more efficient syntheses of polycyclic diterpenes through intramolecular cyclopropanation of aryl rings in diazomethyl ketones
- Catalytic asymmetric carbon-carbon bond-forming reaction utilizing rare earth metal complexes
- Chiral animals: Powerful auxiliaries in asymmetric synthesis
- Recent developments in palladium-catalyzed oxidations
- Cyclopropyl compounds as chemical building blocks: Total syntheses of the alkaloids (-)-colchicine, imerubrine and grandirubrine
- Selective organic synthesis via group 6 metal carbene complexes
- The Birch reduction in organic synthesis
- A general method for the synthesis of bridged indole alkaloids
- Diastereoselective reactions of enolates
- Studies directed towards the development of cyclic peptide-based analogs of macrolide immunosuppressants
- Recent advances in the development of highly enantioselective synthetic methods
- Synthesis of natural g-lactones and a dilactone pyrrolizidine alkaloid via the reactions of 2-propenyl-1,3-dithiane
- Open chain 1,3-stereocontrol
- Carbohydrate building blocks in heterocyclic chemistry. Synthetic studies directed towards the herbicidins
- New asymmetric synthesis of β-hydroxy α-amino acids and analogues. Components of biologically active cyclopeptides
- Synthesis of cyclopentanoids - a never ending challenge
- Synthesis of the 'enediyne' antibiotic esperamicin-A1, and novel analogues for tumor targeting
- Search for antibody catalysts for the ene reaction
- Novel synthetic strategy for HMG-CoA reductase inhibitors
- Heteroatom-directed lithiations of chiral alkyl carbamates: A powerful tool for enantioselective synthesis
- Cobalt(II) Schiff base catalyzed biomimetic oxidation of organic substrates with dioxygen
- Radical cyclizations involving the evolution of nitrogen
- Hypervalent iodine reagents in organic synthesis: Nucleophilic substitution of p-substituted phenol ethers
- Oxacycle synthesis via radical cyclization of β-alkoxyacrylates
- Regioselective C-O bond cleavage reactions of acetals
- Asymmetric calysis of carbonyl-ene reactions and related carbon-carbon bond forming reactions
- Asymmetric synthesis of α,α-disubstituted α-amino acids
- Design of [1,n]-ambiphiles based on zincate carbenoid chemistry
- Design of a photosystem to harvest visible-light into electrons: Photosensitised one electron redox reactions in organic synthesis
- Synthetic studies on manzamine A
- Syntheses of chiral amino alcohols and diols
- Organotitanium compounds in organic synthesis
- Design and synthesis of self-assembling peptides
- Photocyclization-fragmentation route to di- and triquinanes: Stereocontrolled asymmetric synthesis of (-)-isocomene
- Regio- and stereoselective metal-mediated synthesis of polyfunctionalized alkenes
- The Michael-Aldol condensation approach to the construction of key intermediates in the synthesis of terpenoid natural products
- α-Carbonyl radicals for total synthesis of natural products
- Recent advances in asymmetric synthesis using chiral lithium amide bases
- New applications of chiral N-acyliminium precursors
- Synthetic approaches to homogynolides A and B
- Synthesis and cytotoxicity of natural (-)-quinocarcin and its related compounds
- Aspects of remote asymmetric induction using allylstannanes
- Diastereofacial control in the radical addition to chiral α-sulfinyl enones
- Towards the asymmetric synthesis of bryostatin 1
- 'Naked sugars of the second generation': Asymmetric synthesis of long-chain polypropionates and analogues starting with acetone
- Regiospecific synthesis of 3,4-disubstituted furans
- Stereoselective synthesis of acyclic natural products containing chiral vicinal diol
- Aziridine and azirine carboxylic esters
- Novel reaction products from simple organic reactions: Delineation of reaction pathways
- Synthesis of substituted imidazoles and uracils as herbicides
- Microbial metabolites - an infinite source of novel chemistry
- Preparative and mechanistic aspects of inter-estification reactions on diols and peracetylated polyphenolic compounds catalysed by lipases
- Metalloporphyrins as chemical mimics of cytochrome P-450 systems
- Molecular recognition and signalling
- Efficient syntheses of regioisomers of tiagabine
- Synthesis and spectral studies of natural chlorins having antioxidative activity
- The synthesis of taxoids from glucose
- Use of 1-menthyl ester as chiral auxiliary in the synthesis of useful chiral synthons