Hetero Diels-Alder Reactions in Organic Chemistry
出版社:
Springer Berlin Heidelberg
摘要:
The hetero Diels-Alder reaction is one of the most important methods for the synthesis of heterocycles. In this article an overview is given for the period since 1989 describing the reaction of heterobutadienes such as oxabutadienes, thiabutadienes, azabutadienes, diaazabutadienes, nitroso-alkenes and nitroalkenes as well as of heterodienophiles such as carbonyls, thiocarbonyls, imines, iminium salts, azo- and nitroso compounds. In addition, several other less common hetero Diels-Alder reactions such as cycloadditions of thiaazabutadienes, oxaazabutadienes, dioxabutadienes, dithiabutadienes, oxathiabutadienes, diazaoxabutadienes as well as the use of N-sulfinyl-phosphaalkynes and other dienophiles are mentioned. A main point of discussion is the stereoselectivity of the reactions and the preparation of enantiopure compounds either using dienes and dienophiles carrying a chiral auxiliary or employing chiral Lewis acids. A point stressed is the synthesis of natural products using hetero Diels-Alder reactions leading to carbohydrates, alkaloids, terpenes, antibiotics, mycotoxins, cytochalasans, antitumor agents and several other classes of natural products.Another topic is the use of high pressure in hetero Diels-Alder reactions discussing the influence on the rate constants and the stereoselectivity. Finally, modern developments such as reactions on solid phase, the use of catalytic monoclonal antibodies, transformations in aqueous solution and the microwave activation are described.
展开
关键词:
Diels-Alder reaction cycloaddition azabutadienes oxabutadienes diastereoselectivity enantioselectivity heterocycles natural products high pressure Lewis acids
出版时间:
1997
被引量:
通过文献互助平台发起求助,成功后即可免费获取论文全文。
相似文献
引证文献
同作者
引用走势
辅助模式
引用
文献可以批量引用啦~
欢迎点我试用!