| 書目名稱 | Intramolecular Diels-Alder and Alder Ene Reactions | | 編輯 | Douglass F. Taber | | 視頻video | http://file.papertrans.cn/474/473183/473183.mp4 | | 叢書名稱 | Reactivity and Structure: Concepts in Organic Chemistry | | 圖書封面 |  | | 描述 | The Diels-Alder reaction has long been a powerful tool in organic synthesis. In recent years, the Alder ene reaction has also achieved some prominence. From the beginning, it was apparent that the intramolecular variants of these reactions would be feasible. Many such have been reported, but the results are widely scattered in the chemical literature. This volume is an attempt to synthesize results observed to date, and to suggest directions for future development. One of the limiting factors in the application of the intramolecular Diels- Alder reaction has been the development of methods for the preparation of the requisite trienes. The fIrst chapter of this volume summarizes methods for the preparation of dienes and dienophiles. Examples representative of every general approach to 1,3-dienes and to dienophilic functional group combinations have been included. There are two questions one might ask in considering the prospective cyclization of a given triene: what are the factors that govern the rate of cyclization? and, for cyclizations that lead to the creation of one or more new chiral centers, what are the factors that govern diastereoselectivity? These questions are addressed | | 出版日期 | Book 1984 | | 關(guān)鍵詞 | Diastereomer; Diensynthese; En-Synthese; Ene reaction; Reactions; Transition state; catalysis; development; | | 版次 | 1 | | doi | https://doi.org/10.1007/978-3-642-69233-8 | | isbn_softcover | 978-3-642-69235-2 | | isbn_ebook | 978-3-642-69233-8Series ISSN 0341-2377 | | issn_series | 0341-2377 | | copyright | Springer-Verlag Berlin Heidelberg 1984 |
The information of publication is updating
|
|
|Archiver|手機(jī)版|小黑屋|
派博傳思國際
( 京公網(wǎng)安備110108008328)
GMT+8, 2026-1-27 11:22
發(fā)表于 2025-3-21 17:46:12
