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Titlebook: Intramolecular Diels-Alder and Alder Ene Reactions; Douglass F. Taber Book 1984 Springer-Verlag Berlin Heidelberg 1984 Diastereomer.Diensy

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書目名稱Intramolecular Diels-Alder and Alder Ene Reactions
編輯Douglass F. Taber
視頻videohttp://file.papertrans.cn/474/473183/473183.mp4
叢書名稱Reactivity and Structure: Concepts in Organic Chemistry
圖書封面Titlebook: Intramolecular Diels-Alder and Alder Ene Reactions;  Douglass F. Taber Book 1984 Springer-Verlag Berlin Heidelberg 1984 Diastereomer.Diensy
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
doihttps://doi.org/10.1007/978-3-642-69233-8
isbn_softcover978-3-642-69235-2
isbn_ebook978-3-642-69233-8Series ISSN 0341-2377
issn_series 0341-2377
copyrightSpringer-Verlag Berlin Heidelberg 1984
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Reactivity and Structure: Concepts in Organic Chemistryhttp://image.papertrans.cn/i/image/473183.jpg
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The Intramolecular Diels-Alder Reaction: Reactivity and Stereocontrol,thods by which they can be prepared. This chapter addresses two other areas of interest : the factors that govern the rate of the intramolecular Diels- Alder reaction, and, in reactions leading to the formation of one or more new chiral centers, the factors that govern the stereochemical outcome of the cyclization.
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發(fā)表于 2025-3-22 07:06:27 | 只看該作者
978-3-642-69235-2Springer-Verlag Berlin Heidelberg 1984
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The Intramolecular Diels-Alder Reaction: Variations and Scope,en because efficient routes to the requisite trienes have only recently been available, and partly it has been because there has not been enough data in the literature to allow one to predict with confidence the stereochemical outcome of a prospective cyclization.
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0341-2377 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 direc
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Book 1984ne 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
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