Study on the Mechanism of Pd(0) Catalyzed Hydrostannation of Conjugated Dienes by Deuterostannation
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概要
- 論文の詳細を見る
- 1992-06-05
著者
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Yamamura Kimiaki
Department Of Chemistry College Of General Education Kobe University
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Miyake Hideyoshi
Department Of Agrobioscience Graduate School Of Agricultural Science Kobe University
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MIYAKE Hideyoshi
Department of Chemistry, College of General Education, Kobe University
関連論文
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- Crystal Structure of 1, 1, 1-Triphenyl-4-(10-benz[a]azulenyl)-3, 4-buten-2-one
- Crystal Structure of 6,7-Dimethoxy-triptycenequinone
- Synthesis and Seed Germination Stimulating Activity of Some Imino Analogs of Strigolactones
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- Z-and threo-Selective 1-Methyl-2-butenylation of Aldehydes by 4-(Tributylstannyl)-2-pentene
- Z-Selective Synthesis of Homoallylic Alcohols via 2-Alkenylation of Aldehydes by 1-(Tributylstannyl)-2-alkene
- BuSnCl_3-Mediated Reaction of 3-(Tributylstannyl)cycloalkenes with Aldehydes. Highly erythro-Selective 2-Cyclopentenylation and 2-Cyclohexenylation of Aromatic Aldehydes
- On the Transmetallation of (E)-1-Phenyl-3-(tributylstannyl)propene and 3-Phenyl-3-(tributylstannyl)propene with BuSnCl_3
- BuSnCl_3 Mediated Z-Selective 2-Butenylation and erythro-Selective 1-Methyl-2-propenylation of Aldehydes by 1-(Tributylstannyl)-2-butene
- Study on the Mechanism of Pd(0) Catalyzed Hydrostannation of Conjugated Dienes by Deuterostannation
- A Facile Synthesis of Cyclohepta[a]thieno[c]naphthalenylium Ions. Intramolecular Cyclization of o-Thienylcycloheptatrienylbenzenes
- Molecular Dynamics of Octyl Urea Crystals Analyzed by Solid-state NMR
- Conformational adaptation: A new aspect of substitutent effects.
- Three-dimensionally-modified tetracyanoquinodimethanes and their charge-transfer complexes with tetrathiafulvalene derivatives having a wide range of ionicity.
- Free radical addition of thiophenol to 3-substituted 1-alkyne with or without migration of the substituents.
- Formation of 2-substituted 1,3-diphenylindenes by an N-bromosuccinimide prompted dehydrocyclization of 2-substituted 1,3,3-triphenyl-1-propenes.
- Replacement of the activated nitro group by a phenylthio group.