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200228s2020 mau o 001 0 eng d |
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|a YDX
|b eng
|e pn
|c YDX
|d OPELS
|d OCLCF
|d OCLCQ
|d EBLCP
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|a 1142523876
|a 1143618629
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|a 9780128197905
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|z 0128211687
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|a (OCoLC)1137841124
|z (OCoLC)1142523876
|z (OCoLC)1143618629
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4 |
|a QD400
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| 082 |
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4 |
|a 547.59
|2 23
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| 245 |
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|a Advances in heterocyclic chemistry.
|n Volume 132 /
|c edited by Eric F.V. Scriven, Christopher A. Ramsden.
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| 260 |
|
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|a Cambridge, MA :
|b Academic Press,
|c 2020.
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| 300 |
|
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|a 1 online resource
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a Issn Ser.
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| 500 |
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|a Includes index.
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| 505 |
0 |
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|a Front Cover -- Advances in Heterocyclic Chemistry -- Copyright -- Contents -- Contributors -- Preface -- Chapter One: Application of electrochemical oxidative methods in the C(sp)H functionalization of heterocyclic compounds -- 1. Introduction -- 2. CC bond formation -- 2.1. Alkylation -- 2.2. Arylation -- 2.3. Cyanation -- 3. CN bond formation -- 4. CO bond formation -- 5. CP, CS bonds formation -- 6. CHalide bond formation -- 7. Conclusion -- Acknowledgments -- References -- Chapter Two: Recent developments in the chemistry of sydnones and sydnone imines -- 1. Sydnones -- 1.1. Introduction
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| 505 |
8 |
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|a 1.2. Preparation of sydnones -- 1.3. Reactions with retention of the oxadiazole ring -- 1.3.1. Electrophilic substitution -- 1.3.1.1. Halogenation -- 1.3.1.2. Chlorosulfonylation -- 1.3.1.3. Acylation -- 1.3.1.4. Miscellaneous electrophilic substitution reactions at C(4) -- 1.3.2. Direct arylation, alkenylation, and alkynylation of sydnones -- 1.3.3. Reactions of 4-halogeno-substituted sydnones -- 1.3.4. Reactions of 4-formylsydnones -- 1.3.4.1. Synthesis of imines -- 1.3.4.2. 3-Arylsydnone-4-carbohydroximic acid chlorides -- 1.3.4.3. Knoevenagel condensation
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| 505 |
8 |
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|a 1.3.5. Reactions of 4-acetylsydnones -- 1.3.6. Organometallic derivatives -- 1.3.6.1. Lithio derivatives -- 1.3.6.2. Transition metal complexes -- 1.3.7. Side-chain reactions -- 1.4. Sydnone reactions associated with oxadiazole ring opening -- 1.4.1. Cycloaddition reactions -- 1.4.1.1. Introduction -- 1.4.1.2. [3+2]-Cycloaddition of sydnones with alkynes -- 1.4.1.3. Strain-promoted sydnone cycloadditions -- 1.4.1.4. Copper-catalyzed sydnone-alkyne cycloaddition reactions -- 1.4.1.5. [3+2]-Cycloaddition of sydnones with arynes -- 1.4.1.6. [3+2]-Cycloaddition of sydnones with alkenes
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| 505 |
8 |
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|a 1.4.1.7. Miscellaneous cycloadditions -- 1.4.1.8. Syntheses of 1,3,4-oxadiazolin-2-ones -- 1.4.2. Masked hydrazines and other reaction -- 1.5. Biological activity of sydnone derivatives -- 1.6. Sydnones in polymer chemistry -- 1.7. Liquid crystal, optical, and electrochemical properties of sydnones -- 2. Sydnone imines -- 2.1. Preparation of sydnone imines -- 2.2. Reactions of sydnone imines -- 2.2.1. Reactions at the exocyclic N6 atom of sydnone imines -- 2.2.2. Reactions at C(4)-position -- 2.2.2.1. 4-Halogen-substituted derivatives -- 2.2.2.2. 4-Lithium derivatives
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| 505 |
8 |
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|a 2.2.3. Transition metal derivatives of sydnone imines -- 2.2.4. Side-chain reactions -- 2.3. Bicyclic sydnone imines -- 2.4. Cycloaddition of sydnone imines -- 2.5. Biologically activity of sydnone imines -- Acknowledgments -- References -- Chapter Three: The chemistry of thieno[b]pyrrolones, dihydrothieno[b]pyrrolones, and their fused derivatives -- 1. Introduction -- 2. Thieno[2,3-b]pyrrolones -- 2.1. Thieno[2,3-b]pyrrol-2-ones -- 2.1.1. Properties -- 2.1.1.1. Nuclear magnetic resonance spectroscopy -- 2.1.1.2. Infrared spectroscopy -- 2.1.2. Reactivity -- 2.1.2.1. Reaction with nucleophiles
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| 650 |
|
0 |
|a Heterocyclic chemistry.
|
| 650 |
|
6 |
|a Chimie des compos�es h�et�erocycliques.
|0 (CaQQLa)201-0308175
|
| 650 |
|
7 |
|a Heterocyclic chemistry
|2 fast
|0 (OCoLC)fst00955735
|
| 700 |
1 |
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|a Scriven, Eric F. V.
|
| 700 |
1 |
|
|a Ramsden, Christopher A.,
|d 1946-
|
| 776 |
0 |
8 |
|i Print version:
|t Advances in heterocyclic chemistry. Volume 132.
|d Cambridge, MA : Academic Press, 2020
|z 0128211687
|z 9780128211687
|w (OCoLC)1111975705
|
| 830 |
|
0 |
|a Issn Ser.
|
| 856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/bookseries/00652725/132
|z Texto completo
|
