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Author : Chung He Youn
Publisher :
ISBN 13 :
Total Pages : 106 pages
Book Rating : 4.:/5 (978 download)
Download or read book The Study of Stereochemistry of the Diels Alder Reaction written by Chung He Youn and published by . This book was released on 1967 with total page 106 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Laura M. Henry
Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (87 download)
Download or read book A Study of the Stereochemistry of the Diels-Alder Reaction written by Laura M. Henry and published by . This book was released on 1988 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Hugh J. Barger
Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (391 download)
Download or read book A Stereochemical Study of the Diels-Alder Reaction written by Hugh J. Barger and published by . This book was released on 1965 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Glenn Earl Palmer
Publisher :
ISBN 13 :
Total Pages : 108 pages
Book Rating : 4.:/5 (219 download)
Download or read book Stereochemical Studies Related to the Diels-Alder Reaction written by Glenn Earl Palmer and published by . This book was released on 1962 with total page 108 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : James Grubbs Martin
Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (842 download)
Download or read book Stereochemistry of the Diels-Alder Reaction written by James Grubbs Martin and published by . This book was released on 1960 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Francesco Fringuelli
Publisher : John Wiley & Sons
ISBN 13 : 9780471803430
Total Pages : 364 pages
Book Rating : 4.8/5 (34 download)
Download or read book The Diels-Alder Reaction written by Francesco Fringuelli and published by John Wiley & Sons. This book was released on 2002-01-21 with total page 364 pages. Available in PDF, EPUB and Kindle. Book excerpt: 70 Jahre Forschung an der Diels-Alder-Reaktion: Dieses Buch fasst die wichtigsten und beeindruckendsten Ergebnisse in einzigartiger Weise zusammen! Zunächst werden die Grundprinzipien der Reaktion klar und verständlich anhand übersichtlicher Graphiken erläutert. Spezielle Vorschriften und gegebenenfalls ihre industrielle Umsetzung werden anschließend erklärt. Einen Schwerpunkt bilden auch physikalische und katalytische Verfahren zur Steigerung der Selektivität der Reaktion. Cycloadditionen in konventionellen und unkonventionellen Medien werden vorgestellt. Mit über 1.000 Literaturverweisen!
Author : Yuan-Fang Li Hsu
Publisher :
ISBN 13 :
Total Pages : 242 pages
Book Rating : 4.:/5 (253 download)
Download or read book An Aspect of the Stereochemistry of the Diels-Alder Reaction: Syn-anti Isomerism written by Yuan-Fang Li Hsu and published by . This book was released on 1969 with total page 242 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Herbert Russell Gillis
Publisher :
ISBN 13 :
Total Pages : 454 pages
Book Rating : 4.:/5 (15 download)
Download or read book Stereochemical Aspects of the Intramolecular Diels-Alder Reaction written by Herbert Russell Gillis and published by . This book was released on 1982 with total page 454 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Louis Ralph Duckwall
Publisher :
ISBN 13 :
Total Pages : 310 pages
Book Rating : 4.:/5 (737 download)
Download or read book Regiochemistry and Stereochemistry of the Diels-Alder Reaction ; the Synthesis and Reactions of 1,3-cyclohexadienes written by Louis Ralph Duckwall and published by . This book was released on 1980 with total page 310 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : George A. Olah
Publisher : John Wiley & Sons
ISBN 13 : 0471461385
Total Pages : 897 pages
Book Rating : 4.4/5 (714 download)
Download or read book Hydrocarbon Chemistry written by George A. Olah and published by John Wiley & Sons. This book was released on 2003-09-10 with total page 897 pages. Available in PDF, EPUB and Kindle. Book excerpt: Hydrocarbons and their transformations play major roles in chemistry as raw materials and sources of energy. Diminishing petroleum supplies, regulatory problems, and environmental concerns constantly challenge chemists to rethink and redesign the industrial applications of hydrocarbons. Written by Nobel Prize-winner George Olah and hydrocarbon expert Árpád Molnár, the completely revised and expanded Second Edition of Hydrocarbon Chemistry provides an unparalleled contemporary assessment of the field, presenting basic concepts, current research, and future applications. Hydrocarbon Chemistry begins by discussing the general aspects of hydrocarbons, the separation of hydrocarbons from natural sources, and the synthesis from C1 precursors with recent developments for possible future applications. Each successive chapter deals with a specific type of hydrocarbon transformation. The Second Edition includes a new section on the chemical reduction of carbon dioxide–focusing on catalytic, ionic, electrocatalytic, photocatalytic, and ezymatic reductions–as well as a new chapter on new catalysts and activation methods, combinatorial chemistry, and environmental chemistry. Other topics covered include: Major processes of the petrochemical industry, such as cracking, reforming, isomerization, and alkylation Derivation reactions to form carbon-heteroatom bonds Hydrocarbon oxidations Metathesis Oligomerization and polymerization of hydrocarbons All chapters have been updated by adding sections on recent developments to review new advances and results. Essential reading for practicing scientists in industry, polymer and catalytic chemists, as well as researchers and graduate students, Hydrocarbon Chemistry, Second Edition remains the benchmark text in its field.
Author : Geoff T. Halvorsen
Publisher :
ISBN 13 : 9781267315878
Total Pages : 630 pages
Book Rating : 4.3/5 (158 download)
Download or read book Studies on the Intramolecular Diels-Alder Reaction written by Geoff T. Halvorsen and published by . This book was released on 2012 with total page 630 pages. Available in PDF, EPUB and Kindle. Book excerpt: The intramolecular Diels-Alder reaction is widely recognized as a powerful and versatile method for the assembly of complex bicyclic structures in synthetic organic chemistry and has been utilized as a key step in the total syntheses of a number of interesting biologically active natural products. We have studied the use of siloxacyclopentene constrained trienes as a method to control diastereofacial selectivity in the intramolecular Diels-Alder reaction. The siloxacyclopentene constraints could be formed under mild conditions and attached to either the diene or dienophile units of a variety of trienes. These constrained trienes underwent intramolecular Diels-Alder reactions to give cycloadducts with the oxygen contained in the siloxacyclopentene exclusively in an anti-configuration relative to the ring fusion proton. Suitably chosen dienophile activating groups and optimized conditions for cyclization allowed for high levels of selectivity for either cis - or trans -fused cycloadducts in the case of siloxacyclopentenes contained within the diene, while siloxacyclopentenes constraints attached at the dienophile gave exclusively the trans-fused cycloadducts. A siloxacyclopentene constrained tetraene was then utilized in a concise, stereoselective synthesis of the decahydrofluorene core common to the hirsutellones. Synthetic efforts targeting the completion of the hirsutellones via a common biosynthetic intermediate were pursued utilizing a macrobenzannulation strategy. This strategy was abandoned due to inability to prepare a suitable benzannulation precursor. Later a strategy of first forming a five membered ring containing analogue was also pursued, but failed due to an inability to convert a suitable ester to the corresponding furan or thiophene.
Author : Samuel Plyler McManus
Publisher :
ISBN 13 :
Total Pages : 114 pages
Book Rating : 4.:/5 (186 download)
Download or read book Stereochemistry of the Diels-Alder Reaction with Cis- and Trans-benzalacetone and Acetylphenylacetylene written by Samuel Plyler McManus and published by . This book was released on 1962 with total page 114 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Alexander Graham Fallis
Publisher :
ISBN 13 :
Total Pages : 164 pages
Book Rating : 4.:/5 (219 download)
Download or read book Stereochemical Studies of Diels-Alder Adducts written by Alexander Graham Fallis and published by . This book was released on 1964 with total page 164 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Harry Robert Musser
Publisher :
ISBN 13 :
Total Pages : 68 pages
Book Rating : 4.:/5 (596 download)
Download or read book Stereochemistry of Chlorinated Diels-Alder Adducts written by Harry Robert Musser and published by . This book was released on 1965 with total page 68 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Hexachlorocyclopentadiene and related compounds have been studied extensively in connection with Diels-Alder reactions. Many of the adducts formed are used as intermediates in insecticide syntheses. It is of interest to study the stereochemistry of the adducts of one of the hexachlorocyclopentadiene derivaites. 5,5-Dimethoxy-1,2,3,4-tetrachlorocyclopentadiene and various dienophiles, when allowed to react, yield compounds of the bridges bicyclo [2.2.1] hept-2-ene series. The study of the endo and/or exo configuration of various functional groups such as carboxyl, aldehyde, and hydroxymethyl can be related to the known exo-5-hydroxymethyl1-1,2,3,4-tetrachlorobicyclo-[2.2.1] help-2-ene-7-one"--Introduction, leaf [1].
Author : W. Carruthers
Publisher : Elsevier
ISBN 13 : 008091232X
Total Pages : 382 pages
Book Rating : 4.0/5 (89 download)
Download or read book Cycloaddition Reactions in Organic Synthesis written by W. Carruthers and published by Elsevier. This book was released on 2013-10-22 with total page 382 pages. Available in PDF, EPUB and Kindle. Book excerpt: Demonstrates the wide scope of cycloaddition reactions, including the Diels-Alder reaction, the ene reaction, 1,3-dipolar cycloadditions and [2+2] cycloadditions in organic synthesis. The author, a leading exponent of the subject, illustrates the ways in which they can be employed in the synthesis of a wide range of carbocyclic and heterocyclic compounds, including a variety of natural products of various types. Special attention is given to intramolecular reactions, which often provide a rapid and efficient route to polycyclic compounds, and to the stereochemistry of the reactions, including recent and developing work on enantioselective synthesis.
Download or read book A Theoretical Study of Stereoselectivity in the Diels-Alder Reaction written by and published by . This book was released on 1999 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Ryan C. Clark
Publisher :
ISBN 13 :
Total Pages : 560 pages
Book Rating : 4.:/5 (763 download)
Download or read book I. An Asymmetric Variant of the 1-azadiene Diels-Alder Reaction. II. Total Synthesis, Stereochemical Reassignment and Absolute Configuration of Chlorofusin written by Ryan C. Clark and published by . This book was released on 2008 with total page 560 pages. Available in PDF, EPUB and Kindle. Book excerpt: Although the inverse electron demand Diels-Alder reaction of N-sulfonyl-1-aza-1,3-butadienes with electron-rich dienophiles has been extensively examined in our laboratory, we sought to control the absolute configuration of the tetrahydropyridine products and thereby extend the utility of the methodology. The first detailed study of a room temperature asymmetric Diels-Alder reaction of N-sulfonyl-1-aza-1,3-butadienes enlisting a series of nineteen enol ethers bearing chiral auxilaries is described herein. Many of these auxilaries provided highly diastereoselective reactions (in both the endo and facial sense) largely the result of a highly organized [4+2] cycloaddition transition state. Three readily accessible and previously unexplored butyrolactone and pyrrolidinone auxilaries rationally emerged from the studies and provide exceptional selectivities (up to 49:1 endo:exo and 48:1 facial).
