Titlebook: Enantiomer Separation; Fundamentals and Pra Fumio Toda Book 2004 Springer Science+Business Media B.V. 2004 chromatography.crystal.crystalli

Corrugate

書(shū)目名稱Enantiomer Separation影響因子(影響力)




書(shū)目名稱Enantiomer Separation影響因子(影響力)學(xué)科排名




書(shū)目名稱Enantiomer Separation網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱Enantiomer Separation網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱Enantiomer Separation被引頻次




書(shū)目名稱Enantiomer Separation被引頻次學(xué)科排名




書(shū)目名稱Enantiomer Separation年度引用




書(shū)目名稱Enantiomer Separation年度引用學(xué)科排名




書(shū)目名稱Enantiomer Separation讀者反饋




書(shū)目名稱Enantiomer Separation讀者反饋學(xué)科排名

Robust

Crystalline dipeptides: their molecular recognition to be useful to enantiomer separation,clusion crystals creates one of the most useful and informative fields of molecular recognition. Hitherto, the phenomena that host molecules form crystals with appropriate guest molecules have been investigated.1 Inclusion crystals of urea and bile acid were investigated at the early stage of this f

CRASS

甜瓜

Book 2004owadays, the descriptions “enantiomer resolution” or “enantiomer separation” are also commonly used. Accordingly, “Enantiomer Separation” is used in the title of this book. The editor and all chapter contributors hope that this book is helpful for scientists and engineers working in this field.

Eosinophils

,Optical resolution via complex formation with O,O’-dibenzoyltataric acid,c alcohols have been reviewed in this chapter. Practical and theoretical aspects of these optical resolution processes have also been discussed..Key words: optical resolution, diastereoisomeric complexes, O,O’-dibenzoyltartaric acid, hydroxycarboxylic acid esters, hydroxycarboxylic acids, chiral phosphine oxides, r racemic alcohols.

相容

Optical resolution by means of crystallization,of racemates via crystallization is still a useful key technology for preparing optically active compounds in an industrial-scale production. In this chapter, we deal with resolutions involving crystallization techniques, i.e. preferential crystallization and diastereomeric crystallization.

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grenade

tely different from those edited previously from the viewpoiIn spite of important advances in asymmetric synthesis, chiral compounds cannot all be obtained in a pure state by asymmetric synthesis. As a result, enantiomer separation remains an important technique for obtaining optically active materi

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公理

of racemates via crystallization is still a useful key technology for preparing optically active compounds in an industrial-scale production. In this chapter, we deal with resolutions involving crystallization techniques, i.e. preferential crystallization and diastereomeric crystallization.