|
|
|
|
LEADER |
00000cam a2200000 i 4500 |
001 |
SCIDIR_on1061292600 |
003 |
OCoLC |
005 |
20231120010324.0 |
006 |
m o d |
007 |
cr un|---aucuu |
008 |
181106s2018 ne ob 001 0 eng d |
040 |
|
|
|a OPELS
|b eng
|e rda
|e pn
|c OPELS
|d OPELS
|d N$T
|d OCLCF
|d MERER
|d YDXIT
|d D6H
|d VT2
|d OCLCQ
|d UKMGB
|d YDX
|d LQU
|d S2H
|d OCLCO
|d OCLCQ
|d OCLCO
|d SFB
|d OCLCQ
|d OCLCO
|
016 |
7 |
|
|a 019086991
|2 Uk
|
019 |
|
|
|a 1065380303
|a 1079186359
|a 1105184403
|a 1105559852
|
020 |
|
|
|a 9780081027899
|q (electronic bk.)
|
020 |
|
|
|a 0081027893
|q (electronic bk.)
|
020 |
|
|
|z 9780081027882
|q (print)
|
020 |
|
|
|z 0081027885
|
035 |
|
|
|a (OCoLC)1061292600
|z (OCoLC)1065380303
|z (OCoLC)1079186359
|z (OCoLC)1105184403
|z (OCoLC)1105559852
|
050 |
|
4 |
|a QD400
|b .P76 2018
|
072 |
|
7 |
|a SCI
|x 013040
|2 bisacsh
|
082 |
0 |
4 |
|a 547/.59
|2 23
|
245 |
0 |
0 |
|a Progress in heterocyclic chemistry.
|n Volume 30 /
|c edited by Gordon Gribble, John Joule.
|
264 |
|
1 |
|a Amsterdam, Netherlands :
|b Elsevier,
|c [2018]
|
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
|
490 |
0 |
|
|a Progress in Heterocyclic Chemistry ;
|v Volume 30
|
504 |
|
|
|a Includes bibliographical references and index.
|
500 |
|
|
|a Title from title details screen.
|
505 |
0 |
|
|a Front Cover -- PROGRESS IN HETEROCYCLIC CHEMISTRY -- PROGRESS IN HETEROCYCLIC CHEMISTRY -- Copyright -- CONTENTS -- CONTRIBUTORS -- FOREWORD -- EDITORIAL ADVISORY BOARD MEMBERS PROGRESS IN HETEROCYCLIC CHEMISTRY -- 1 -- Nitrogen-Philic Cyclization of Acyl Radicals Enables the Synthesis of Lactams -- 1.1 INTRODUCTION -- 1.1.1 Exo Cyclization of Acyl Radicals Onto Imine N-C Double Bond -- 1.1.2 Endo Cyclization of Acyl Radicals Onto Imine CN Double Bond -- 1.2 ACYL RADICAL CYCLIZATION ONTO AMINE NITROGEN -- 1.3 ACYL RADICAL CYCLIZATION ONTO AZIDE NITROGEN -- 1.4 SYNTHESIS OF LACTAMS VIA [2+2+1] CYCLOADDITION -- 1.5 AMINOCARBONYLATION LEADING TO LACTAMS -- 1.6 CONCLUSIONS -- REFERENCES -- 2 -- The Silyl-Prins Reaction as an Emerging Method for the Synthesis of Heterocycles -- 2.1 INTRODUCTION -- 2.2 SYNTHESIS OF OXACYCLES BY SILYL-PRINS CYCLIZATIONS WITH ALLYLSILANES -- 2.2.1 Synthesis of Five-Membered Oxacycles -- 2.2.2 Synthesis of Six-Membered Oxacycles -- 2.2.2.1 Synthesis of Dihydropyrans and Tetrahydropyrans -- 2.2.2.2 Synthesis of Methylenetetrahydropyrans -- 2.3 SYNTHESIS OF SEVEN- TO TEN-MEMBERED OXACYCLES -- 2.3.1 Oxepanes -- 2.3.2 Oxocanes -- 2.3.3 Macrocyclic Systems -- 2.3.4 Synthesis of Bicycles -- 2.4 SYNTHESIS OF OXACYCLES BY SILYL-PRINS CYCLIZATIONS WITH VINYLSILANES -- 2.4.1 Synthesis of Five-Membered Oxacycles -- 2.4.2 Synthesis of Six-Membered Oxacycles -- 2.4.3 Synthesis of Seven-Membered Oxacycles -- 2.4.4 Synthesis of Bicycles -- 2.5 SYNTHESIS OF AZACYCLES BY SILYL-AZA-PRINS CYCLIZATIONS -- 2.5.1 Allyl Silanes -- 2.5.1.1 Five-Membered Azacycles -- 2.5.1.2 Six-Membered Azacycles -- 2.5.1.3 Seven-Membered Azacycles -- 2.5.1.4 Bicyclic Systems -- 2.5.2 Vinyl Silanes -- 2.5.2.1 Six-Membered Azacycles -- 2.5.2.2 Bicyclic Systems -- 2.6 OTHER SILANES -- 2.7 SUMMARY -- REFERENCES -- 3 -- Three-Membered Ring Systems -- 3.1 INTRODUCTION.
|
505 |
8 |
|
|a 5.2.4.1.3 Intramolecular Type c -- 5.2.4.1.4 Intramolecular Type e -- 5.2.4.2 Intermolecular Approaches to Indoles -- 5.2.4.2.1 Intermolecular Type ab -- 5.2.4.2.2 Intermolecular Type ac -- 5.2.4.2.3 Intermolecular Type bc -- 5.2.4.2.4 Intermolecular Type ce -- 5.2.4.2.5 Other Intermolecular Syntheses of Indole -- 5.2.5 REACTIONS OF INDOLES -- 5.2.5.1 Substitution at C2/C3 -- 5.2.5.1.1 C2 Substitution -- 5.2.5.1.1.1 Directed C-H Functionalization -- 5.2.5.1.1.2 Innate C-H Functionalization -- 5.2.5.1.2 C2 Substitution, Ring-Forming -- 5.2.5.1.3 C2-C3 Annulation/Functionalization -- 5.2.5.1.4 C3 Substitution -- 5.2.5.1.5 C3 Substitution, Ring-Forming -- 5.2.5.2 Substitution at Nitrogen -- 5.2.5.3 Functionalization of the Benzene Ring -- 5.2.5.3.1 C-H Functionalization -- 5.2.5.3.2 From Prefunctionalized Indoles (e.g., Halides, Triflates, etc.) -- 5.2.6 ISATINS, OXINDOLES, INDOXYLS, AND SPIROOXINDOLES -- 5.2.7 CARBAZOLES -- 5.2.8 AZAINDOLES -- 5.2.9 ISOINDOLES -- REFERENCES -- 5.3 -- Five-Membered Ring Systems: Furans and Benzofurans -- 5.3.1 INTRODUCTION -- 5.3.2 REACTIONS -- 5.3.2.1 Furans -- 5.3.3 SYNTHESIS -- 5.3.3.1 Furans -- 5.3.3.2 Benzo[b]furans and Related Compounds -- ACKNOWLEDGMENTS -- REFERENCES -- 5.4 -- Five-Membered Ring Systems: With More Than One N Atom -- 5.4.1 INTRODUCTION -- 5.4.2 PYRAZOLES AND RING-FUSED DERIVATIVES -- 5.4.3 IMIDAZOLES AND RING-FUSED DERIVATIVES -- 5.4.4 1,2,3-TRIAZOLES AND RING-FUSED DERIVATIVES -- 5.4.5 1,2,4-TRIAZOLES AND RING-FUSED DERIVATIVES -- 5.4.6 TETRAZOLES AND RING-FUSED DERIVATIVES -- REFERENCES -- 5.5 -- Five-Membered Ring Systems: With N and S Atoms -- 5.5.1 INTRODUCTION -- 5.5.2 THIAZOLES -- 5.5.2.1 Synthesis of Thiazoles -- 5.5.2.2 Synthesis of Thiazolines -- 5.5.2.3 Synthesis of Benzothiazoles -- 5.5.2.4 Reactions of Thiazoles and Fused Derivatives -- 5.5.2.5 New Thiazole-Containing Natural Products.
|
505 |
8 |
|
|a 5.5.2.6 Biologically Active Thiazoles and Isothiazoles -- 5.5.3 ISOTHIAZOLES -- 5.5.4 THIADIAZOLES -- REFERENCES -- 5.6 -- Five-Membered Ring Systems: With O and S (Se, Te) Atoms -- 5.6.1 1,3-DIOXOLES AND DIOXOLANES -- 5.6.2 1,3-DITHIOLES AND DITHIOLANES -- 5.6.3 1,3-OXATHIOLES AND OXATHIOLANES -- 5.6.4 1,2-DITHIOLES AND DITHIOLANES -- 5.6.5 THREE HETEROATOMS -- REFERENCES -- 5.7 -- Five-Membered Ring Systems: With O and N Atoms -- 5.7.1 ISOXAZOLES -- 5.7.2 ISOXAZOLINES -- 5.7.3 ISOXAZOLIDINES -- 5.7.4 OXAZOLES -- 5.7.5 OXAZOLINES -- 5.7.6 OXAZOLIDINES -- 5.7.7 OXADIAZOLES -- REFERENCES -- 6.1 -- Six-Membered Ring Systems: Pyridine and Benzo Derivatives -- 6.1.1 INTRODUCTION -- 6.1.2 PYRIDINES -- 6.1.2.1 Preparation of Pyridines -- 6.1.2.2 Reactions of Pyridines -- 6.1.3 QUINOLINES -- 6.1.3.1 Preparation of Quinolines -- 6.1.3.2 Reactions of Quinolines -- 6.1.4 ISOQUINOLINES -- 6.1.4.1 Preparation of Isoquinolines -- 6.1.4.2 Reactions of Isoquinolines -- REFERENCES -- 6.2 -- Six-Membered Ring Systems: Diazines and Benzo Derivatives -- 6.2.1 Introduction -- 6.2.2 Pyridazines and Benzo Derivatives -- 6.2.2.1 Syntheses -- 6.2.2.2 Reactions -- 6.2.2.3 Applications -- 6.2.3 Pyrimidines and Benzo Derivatives -- 6.2.3.1 Syntheses -- 6.2.3.2 Reactions -- 6.2.3.3 Applications -- 6.2.4 Pyrazines and Benzo Derivatives -- 6.2.4.1 Syntheses -- 6.2.4.2 Reactions -- 6.2.4.3 Applications -- References -- 6.3 -- Triazines, Tetrazines, and Fused Ring Polyaza Systems -- 6.3.1 INTRODUCTION -- 6.3.2 TRIAZINES -- 6.3.2.1 1,2,3-Triazines or v-Triazines and 1,2,4-Triazines or a-Triazines -- 6.3.2.2 1,3,5-Triazines (s-Triazines) -- 6.3.2.2.1 Chemistry -- 6.3.2.2.2 Triazines for Material Chemistry -- 6.3.2.2.3 Triazines for Biomedical and Related Applications -- 6.3.2.2.4 Triazines for Fluorescence and Optics-Related Applications -- 6.3.2.2.5 Miscellaneous -- 6.3.3 TETRAZINES.
|
505 |
8 |
|
|a 6.3.3.1 Synthetic Chemistry -- 6.3.3.2 Tetrazines for Click Chemistry and Related Applications -- 6.3.3.3 Applications for Optics: New Dyes -- 6.3.3.4 Miscellaneous -- 6.3.4 FUSED HIGHER POLYAZAAROMATICS -- 6.3.4.1 [6+5] Fused Systems: Purines and Related Heterocycles -- 6.3.4.1.1 Purines and Related Heterocycles -- 6.3.4.2 [6+6] Fused Systems: Pteridines and Related Heterocycles -- 6.3.4.3 New Polyazafused Rings and Heptazines -- REFERENCES -- 6.4 -- Six-Membered Ring Systems: With O and/or S Atoms -- 6.4.1 INTRODUCTION -- 6.4.2 HETEROCYCLES CONTAINING ONE OXYGEN ATOM -- 6.4.2.1 Pyrans -- 6.4.2.2 [1]Benzopyrans and Dihydro[1]benzopyrans -- 6.4.2.2.1 Chromenes and Chromans -- 6.4.2.3 [2]Benzopyrans and Dihydro[2]benzopyrans -- 6.4.2.3.1 Isochromenes and Isochromans -- 6.4.2.4 Pyranones -- 6.4.2.5 Coumarins -- 6.4.2.6 Chromones and Chromanones -- 6.4.2.7 Xanthenes and Xanthones -- 6.4.3 HETEROCYCLES CONTAINING ONE OR TWO SULFUR ATOMS -- 6.4.3.1 Thiopyrans and Analogs -- 6.4.3.2 Dithiin Analogs -- 6.4.4 HETEROCYCLES CONTAINING TWO OR MORE OXYGEN ATOMS -- 6.4.4.1 Dioxanes -- 6.4.5 HETEROCYCLES CONTAINING BOTH OXYGEN AND SULFUR IN THE SAME RING -- 6.4.5.1 Oxathianes -- REFERENCES -- 7 -- Seven-Membered Rings -- 7.1 INTRODUCTION -- 7.2 SEVEN-MEMBERED SYSTEMS CONTAINING ONE HETEROATOM -- 7.2.1 Azepanes and Derivatives -- 7.2.2 Benzazepines and Derivatives -- 7.2.3 Fused Azepanes and Derivatives -- 7.2.4 Oxepanes and Fused Derivatives -- 7.2.5 Thiepines and Fused Derivatives -- 7.3 SEVEN-MEMBERED SYSTEMS CONTAINING TWO HETEROATOMS -- 7.3.1 Diazepines and Fused Diazepines -- 7.3.1.1 Benzodiazepines and Derivatives -- 7.3.2 Oxazepanes and Fused Derivatives -- 7.3.3 Thiazepines and Derivatives -- 7.3.4 Dioxepines, Dithiepines, Oxathiepines, and Derivatives -- 7.4 SEVEN-MEMBERED SYSTEMS CONTAINING THREE OR MORE HETEROATOMS.
|
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
|
655 |
|
7 |
|a periodicals.
|2 aat
|0 (CStmoGRI)aatgf300026657
|
655 |
|
7 |
|a Periodicals
|2 fast
|0 (OCoLC)fst01411641
|
655 |
|
7 |
|a Periodicals.
|2 lcgft
|
655 |
|
7 |
|a P�eriodiques.
|2 rvmgf
|0 (CaQQLa)RVMGF-000001105
|
700 |
1 |
|
|a Gribble, Gordon W.,
|e editor.
|
700 |
1 |
|
|a Joule, J. A.
|q (John Arthur),
|e editor.
|
776 |
0 |
8 |
|i Print version :
|z 9780081027882
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/bookseries/09596380/30
|z Texto completo
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780081027882
|z Texto completo
|