Cargando…

Advances in heterocyclic chemistry. Volume 127.

Detalles Bibliográficos
Clasificación:Libro Electrónico
Formato: Electrónico eBook
Idioma:Inglés
Publicado: [Place of publication not identified] : Elsevier Academic Press, 2019.
Colección:Advances in Heterocyclic Chemistry ; v. 127.
Temas:
Acceso en línea:Texto completo
Texto completo

MARC

LEADER 00000cam a2200000Mi 4500
001 SCIDIR_on1083023835
003 OCoLC
005 20231120010337.0
006 m o d
007 cr |n|||||||||
008 190121s2019 xx ob 001 0 eng d
040 |a YDX  |b eng  |e rda  |e pn  |c YDX  |d N$T  |d EBLCP  |d GZM  |d OPELS  |d OCLCF  |d GZM  |d DKU  |d QCL  |d OCLCQ  |d OCLCO  |d OCLCQ  |d OCLCO 
019 |a 1082356356  |a 1082878784  |a 1089201462  |a 1107840723 
020 |a 9780128171509  |q (electronic bk.) 
020 |a 0128171502  |q (electronic bk.) 
020 |z 0128171812 
020 |z 9780128171813 
020 |z 9780128171493 
035 |a (OCoLC)1083023835  |z (OCoLC)1082356356  |z (OCoLC)1082878784  |z (OCoLC)1089201462  |z (OCoLC)1107840723 
050 4 |a QD400 
072 7 |a SCI  |x 013040  |2 bisacsh 
082 0 4 |a 547.59 
245 0 0 |a Advances in heterocyclic chemistry.  |n Volume 127. 
264 1 |a [Place of publication not identified] :  |b Elsevier Academic Press,  |c 2019. 
300 |a 1 online resource 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
347 |a text file  |b PDF  |2 rda 
490 1 |a Advances in Heterocyclic Chemistry ;  |v Volume 127 
505 0 |a Front Cover; Advances in Heterocyclic Chemistry; Copyright; Contents; Contributors; Preface; Chapter One: Recent advances in 1,2,4-triazolo[1,5-a]pyrimidine chemistry; 1. Introduction; 1.1. General survey; 1.2. Scope and limitation; 1.3. Nomenclature; 2. Occurrence and synthesis; 2.1. Survey; 2.2. Occurrence; 2.3. Syntheses from 5-amino-1,2,4-triazoles and 1,3-biselectrophiles; 2.3.1. Principle and conditions; 2.3.2. The diversity of biselectrophiles; 2.3.3. Regioselectivity; 2.3.4. The direct synthesis of triazolopyrimidines substituted onto carbon ring atoms 
505 8 |a 2.3.5. The use of modified biselectrophiles2.3.6. The use of polyfunctional electrophiles; 2.3.7. Syntheses via dihydro triazolopyrimidines; 2.3.8. Multicomponent reactions; 2.3.9. Special syntheses; 2.4. Syntheses using special aminotriazole derivatives; 2.4.1. Syntheses of N-substituted triazolopyrimidines; 2.4.2. The use of aminotriazole-based intermediates; 2.5. Triazole ring syntheses; 2.5.1. Syntheses from 1,2-diaminopyrimidines; 2.5.2. Syntheses from N-(pyrimid-2-yl)amidine-series compounds; 2.5.3. Syntheses from 2-hydrazinopyrimidines; 2.5.4. Other triazole ring syntheses 
505 8 |a 2.6. Other routes to triazolopyrimidines2.6.1. Aromatization of dihydro derivatives; 2.6.2. Ring transformation and cleavage; 3. Structure; 3.1. Theoretical methods; 3.2. X-ray diffraction; 3.3. Molecular spectra; 3.3.1. H NMR spectra; 3.3.2. C NMR spectra; 3.3.3. F NMR spectra; 3.3.4. Electronic spectra; 3.3.5. Infrared and Raman spectra; 3.3.6. Mass spectra; 3.4. Physicochemical properties; 3.5. Tautomerism; 4. Reactivity; 4.1. Triazolopyrimidines as bases and acids; 4.1.1. Protonation and dissociation; 4.1.2. Coordination; 4.2. Alkylation at nitrogen ring atoms 
505 8 |a 4.3. Carbon-carbon coupling at ring atoms4.3.1. The use of organometallic and metal salt reagents; 4.3.2. Suzuki coupling; 4.3.3. Sonogashira coupling; 4.3.4. Oxidative coupling; 4.3.5. Reductive coupling; 4.3.6. Nucleophilic addition; 4.4. Other reactions at ring atoms; 4.5. Nucleophilic substitution of functional groups at the rings; 4.5.1. Substitution of halogen; 4.5.2. Substitution of oxygen-, sulfur-, or nitrogen-containing functions; 4.6. Transformation of individual substituents; 4.6.1. Oxygen- or sulfur-containing groups; 4.6.2. Amines and their derivatives 
505 8 |a 4.6.3. Carbonyl containing groups4.7. Ring cleavage and recyclization; 4.8. Anellation of heterocyclic rings; 4.8.1. Anellation onto 6/7 positions; 4.8.2. Anellation onto other positions; 4.9. Reactivity of side chains; 4.9.1. Reactions involving halogen or oxygen functionalities; 4.9.2. Reactions involving sulfur, nitrogen, or phosphorus functionalities; 4.9.3. Formation of hydrocarbon groups; 4.9.4. Formation of diheterocyclyl compounds; 5. Application; 5.1. Pharmaceutical use; 5.2. Agrochemical use; 5.3. Optical and information recording uses; 5.4. Other uses; References 
504 |a Includes bibliographical references and index. 
650 0 |a Heterocyclic chemistry. 
650 6 |a Chimie des compos�es h�et�erocycliques.  |0 (CaQQLa)201-0308175 
650 7 |a SCIENCE  |x Chemistry  |x Organic.  |2 bisacsh 
650 7 |a Heterocyclic chemistry  |2 fast  |0 (OCoLC)fst00955735 
776 0 8 |i Print version:  |t Advances in heterocyclic chemistry. Volume 127.  |d [Place of publication not identified] : Elsevier Academic Press, 2019  |z 0128171812  |z 9780128171813  |w (OCoLC)1047773662 
830 0 |a Advances in Heterocyclic Chemistry ;  |v v. 127. 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/bookseries/00652725/127  |z Texto completo 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/bookseries/00652725/127505-00/(S  |z Texto completo