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|a 9783132211810
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|a 3132211818
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|a 547.2
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|a UAMI
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|a Snyder, Scott A., Prof.
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|a Applications of Domino Transformations in Organic Synthesis, Volume 2.
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|a 2nd ed.
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|a NEW YORK :
|b Thieme,
|c 2015.
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|a 1 online resource (534 pages)
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|a text
|b txt
|2 rdacontent
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|a computer
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|2 rdamedia
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|a online resource
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|a Print version record.
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|a Science of Synthesis Applications of Domino Transformations in Organic Synthesis 2; Title Page; Copyright; Preface; Science of Synthesis Reference Library; Volume Editor's Preface; Abstracts; Applications of Domino Transformations in Organic Synthesis 2; Table of Contents; 2.1 Pericyclic Reactions; 2.1.1 The Diels-Alder Cycloaddition Reaction in the Context of Domino Processes; 2.1.1.1 Cascades Not Initiated by Diels-Alder Reaction; 2.1.1.1.1 Cascades Generating a Diene; 2.1.1.1.1.1 Ionic Generation of a Diene; 2.1.1.1.1.1.1 Through Wessely Oxidation of Phenols.
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|a 2.1.1.1.1.1.2 Through Ionic Cyclization2.1.1.1.1.1.3 Through Deprotonation of an Alkene; 2.1.1.1.1.1.4 Through Elimination Reactions; 2.1.1.1.1.1.5 Through Allylation; 2.1.1.1.1.2 Pericyclic Generation of a Diene; 2.1.1.1.1.2.1 Through Electrocyclization; 2.1.1.1.1.2.1.1 Through Benzocyclobutene Ring Opening; 2.1.1.1.1.2.1.2 Through Electrocyclic Ring Closure; 2.1.1.1.1.2.2 Through Cycloaddition or Retrocycloaddition; 2.1.1.1.1.2.3 Through Sigmatropic Reactions; 2.1.1.1.1.3 Photochemical Generation of a Diene; 2.1.1.1.1.4 Metal-Mediated Generation of a Diene.
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|a 2.1.1.1.2 Cascades Generating a Dienophile2.1.1.1.2.1 Ionic Generation of a Dienophile; 2.1.1.1.2.1.1 Through Himbert Cycloadditions; 2.1.1.1.2.1.2 Through Benzyne Formation; 2.1.1.1.2.1.3 Through Wessely Oxidation; 2.1.1.1.2.2 Pericyclic Generation of a Dienophile; 2.1.1.1.2.2.1 Through Cycloaddition/Retrocycloaddition; 2.1.1.1.2.2.2 Through Sigmatropic Rearrangement; 2.1.1.1.2.2.3 Through Electrocyclization; 2.1.1.1.3 Proximity-Induced Diels-Alder Reactions; 2.1.1.2 Diels-Alder as the Initiator of a Cascade; 2.1.1.2.1 Pericyclic Reactions Occurring in the Wake of a Diels-Alder Reaction.
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|a 2.1.1.2.1.1 Cascades Featuring Diels-Alder/Diels-Alder Processes2.1.1.2.1.2 Cascades Featuring Diels-Alder/Retro-Diels-Alder Processes; 2.1.1.2.1.3 [4 + 2] Cycloaddition with Subsequent Desaturation; 2.1.1.2.2 Diels-Alder Reactions with Concomitant Ionic Structural Rearrangements; 2.1.1.2.2.1 Pairings of Diels-Alder Reactions with Structural Fragmentations; 2.1.1.2.2.2 Combining a Diels-Alder Reaction with Ionic Cyclization; 2.1.1.3 Conclusions; 2.1.2 Domino Reactions Including [2 + 2], [3 + 2], or [5 + 2] Cycloadditions; 2.1.2.1 Domino [2 + 2] Cycloadditions.
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|a 2.1.2.1.1 Cycloaddition of an Enaminone and ß-Diketone with Fragmentation2.1.2.1.2 Cycloaddition of Ynolate Anions Followed by Dieckmann Condensation/Michael Reaction; 2.1.2.1.3 Cycloaddition Cascade Involving Benzyne-Enamide Cycloaddition or a Fischer Carbene Complex; 2.1.2.1.4 Cycloadditions with Rearrangement; 2.1.2.1.4.1 Cycloaddition of an Azatriene Followed by Cope Rearrangement; 2.1.2.1.4.2 Cycloaddition of a Propargylic Ether and Propargylic Thioether Followed by [3,3]-Sigmatropic Rearrangement.
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|a 2.1.2.1.4.3 [3,3]-Sigmatropic Rearrangement of Propargylic Ester and Propargylic Acetate Followed by Cycloaddition.
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|a ProQuest Ebook Central
|b Ebook Central Academic Complete
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| 650 |
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|a Organic compounds
|x Synthesis.
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| 650 |
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|a Composés organiques
|x Synthèse.
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| 650 |
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|a Organic compounds
|x Synthesis
|2 fast
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| 758 |
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|i has work:
|a Applications of Domino Transformations in Organic Synthesis, Volume 2 (Text)
|1 https://id.oclc.org/worldcat/entity/E39PD3rcy7mpVVY7Vbj3btDtXd
|4 https://id.oclc.org/worldcat/ontology/hasWork
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| 776 |
0 |
8 |
|i Print version:
|a Snyder, Scott A., Prof.
|t Applications of Domino Transformations in Organic Synthesis, Volume 2.
|d NEW YORK : Thieme, ©2015
|z 9783132211513
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| 856 |
4 |
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|u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=4603521
|z Texto completo
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|a ProQuest Ebook Central
|b EBLB
|n EBL4603521
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|a 92
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