Organoselenium Chemistry: Modern Developments in Organic SynthesisThomas Wirth Springer, 1 de jul. de 2003 - 259 páginas Embarking on a new millennium, the book in hands describes the recent developments of organsoselenium chemistry in all facets. Various distinguished scientists have contributed, with their skill and expertise, making this book a valuable source for synthetic oriented organic chemists and for those, who want to get a first insight into the chemistry of selenium. |
Conteúdo
Nucleophilic Selenium | 55 |
Radical Reactions Using Selenium Precursors | 81 |
SeleniumStabilized Carbanions | 113 |
Selenium at Higher Oxidation State | 143 |
Selenocarbonyls | 177 |
Selenoxide Elimination and 23Sigmatropic Rearrangement | 201 |
Selenium Compounds as Ligands and Catalysts | 234 |
| 256 | |
Outras edições - Ver todos
Organoselenium Chemistry: Modern Developments in Organic Synthesis Thomas Wirth Prévia não disponível - 2014 |
Organoselenium Chemistry: Modern Developments in Organic Synthesis Thomas Wirth Prévia não disponível - 2010 |
Termos e frases comuns
2,3]sigmatropic rearrangement acid addition afforded aldehydes alkenes alkenyl alkyl allylic alcohols aryl selenides asymmetric benzeneselenolate bond carbanion carbon catalytic amount Chem Lett Chem Soc Chem Chem Soc Perkin chiral selenoxides chloride corresponding cyclization reactions derivatives deselenenylation diastereoselective diphenyl diselenide electrophilic electrophilic reagents elemental selenium enantiomeric excess enantioselectivity enolate epoxides esters formation halides heterocyclic hydrogen JAm Chem Soc ketones Krief methyl Murai nitrogen nucleophilic nucleophilic selenium species obtained olefins optically active optically active allylic organic synthesis organoselenium chemistry organoselenium compounds oxidation phenyl phenyl selenides prepared presence radical precursors react reactivity recently reduction reported Scheme 12 selenides selenimides seleniranium intermediate selenium atom selenium compounds selenium dioxide selenium reagents selenium ylides selenoacetals selenoamides selenocarbonyl compounds selenolate selenoxide selenoxide elimination selenurane Soc Chem Commun Soc Perkin Trans sodium stereoselectivity substituents substrates sulfones Synlett Synth Commun synthetic Testaferri Tetrahedron Lett Tiecco Tingoli tion Tomoda Uemura vinyl selenides Wirth yields ylides