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Titlebook: Aldol Reactions; Rainer Mahrwald Book 2009 Springer Science+Business Media B.V. 2009 Aldol Additions.Aldol Methodologies.Base.Enzymes.Lewi

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樓主
發(fā)表于 2025-3-21 16:28:51 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱Aldol Reactions
影響因子2023Rainer Mahrwald
視頻videohttp://file.papertrans.cn/153/152329/152329.mp4
發(fā)行地址Fundamentals of the aldol addition are presented as well as brand new developments in the field of stereoselective aldol additions.The use of metal enolates, Lewis acids, Lewis bases and enzymes in cu
圖書封面Titlebook: Aldol Reactions;  Rainer Mahrwald Book 2009 Springer Science+Business Media B.V. 2009 Aldol Additions.Aldol Methodologies.Base.Enzymes.Lewi
影響因子.Aldol Reactions .provides a comprehensive up-to-date overview of aldol reactions including application of different metal enolates; catalytic aldol additions catalyzed by different Lewis acids and Lewis bases; enantioselective direct aldol additions; antibodies and enzyme catalyzed aldol additions and the recent aggressive development of organocatalyzed aldol additions. ..The power of each method is demonstrated by several applications in total synthesis of natural products. The pros and cons of these methodologies with regard to stereoselectivity, regioselectivity and application in total synthesis of natural products are discussed. Great importance is set to the diverse possibilities of the manual of aldol reaction to install required configurations in complicated natural product synthesis..
Pindex Book 2009
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沙發(fā)
發(fā)表于 2025-3-21 21:54:15 | 只看該作者
Zirconium Lewis Acids,aldol adducts (Scheme 3.1.6.1)...In addition to that, zirconium(IV) alkoxides are able to deprotonate α-carbon atoms of ketones.. By subsequent reactions with aldehydes the corresponding aldol adducts were formed.. The regioselectivity of this aldol addition is illustrated in Scheme 3.1.6.2.
板凳
發(fā)表于 2025-3-22 03:17:29 | 只看該作者
地板
發(fā)表于 2025-3-22 06:40:55 | 只看該作者
Undergraduate Topics in Computer Sciencealdol adducts (Scheme 3.1.6.1)...In addition to that, zirconium(IV) alkoxides are able to deprotonate α-carbon atoms of ketones.. By subsequent reactions with aldehydes the corresponding aldol adducts were formed.. The regioselectivity of this aldol addition is illustrated in Scheme 3.1.6.2.
5#
發(fā)表于 2025-3-22 10:36:43 | 只看該作者
f metal enolates, Lewis acids, Lewis bases and enzymes in cu.Aldol Reactions .provides a comprehensive up-to-date overview of aldol reactions including application of different metal enolates; catalytic aldol additions catalyzed by different Lewis acids and Lewis bases; enantioselective direct aldol
6#
發(fā)表于 2025-3-22 16:11:09 | 只看該作者
https://doi.org/10.1007/978-3-642-69900-9 . in enantioselec-tive aldol additions.. The.-configured aldol adducts were isolated with good enantioselectivities. Furthermore, when used with aromatic ketones enantioselec-tivities up to 90% were detected (Scheme 2.5.1).
7#
發(fā)表于 2025-3-22 20:17:31 | 只看該作者
Data Structures and Algorithms in Swiftehensive, up-to-date overview see Shiina and Fukui.. In contrast to the methods described above the stereoselectivities were strongly influenced by oxygen functionalities of the aldehydes used. These results are summarized in Scheme 3.1.2.1.
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發(fā)表于 2025-3-22 23:22:34 | 只看該作者
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