01037nam0-2200349li-450 99000016834020331620180312154744.00-7514-0041-60016834USA010016834(ALEPH)000016834USA01001683420001109d1995----km-y0itay0103----baengUSPressuremeters in geotechnical designB. G. ClarkeLondon [etc.]Chapman & Hallcopyr. 1995pressiometriprospezione geologica624.1517Prospezioni del terrenoClarke,B. G.753489Sistema bibliotecario di Ateneo dell' Università di SalernoRICA990000168340203316624.151 7 CLA0007329BKTEC1996090220001110USA01171220020403USA011624PATRY9020040406USA011612Pressuremeters in geotechnical design1515761UNISA05354nam 2200697 a 450 991102044780332120200520144314.0978661036786397812803678611280367865978047030766304703076689780471533405047153340897804715337710471533777(CKB)111087027116224(EBL)468793(OCoLC)814412893(SSID)ssj0000231781(PQKBManifestationID)11225886(PQKBTitleCode)TC0000231781(PQKBWorkID)10208995(PQKB)10579166(MiAaPQ)EBC468793(Perlego)2773963(EXLCZ)9911108702711622420040624d2004 uy 0engur|n|---|||||txtccrQuinoxalinesSupplement II /D.J. BrownHoboken, N.J. Wileyc20041 online resource (528 p.)The chemistry of heterocyclic compounds ;v. 61"Interscience publication."9780471264958 0471264954 Includes bibliographical references (p. 437-470) and index.QUINOXALINES Supplement II; Preface; Contents; CHAPTER 1 PRIMARY SYNTHESES; 1.1 From a Single Benzene Substrate; 1.1.1 By Formation of the N1,C8a Bond; 1.1.2 By Formation of the N1,C2 Bond; 1.1.2.1 Cyclization of o-(Ethylamino)aniline Derivatives; 1.1.2.2 Direct Cyclization of o-(Ethylamino)nitrobenzene Derivatives; 1.1.2.3 Reductive Cyclization of o-(Ethylamino)nitrobenzene Derivatives; 1.1.3 By Formation of the C2,C3 Bond; 1.2 From a Benzene Substrate with an Ancillary Synthon; 1.2.1 When the Synthon Supplies N1 of the Quinoxaline; 1.2.2 When the Synthon Supplies C2 of the Quinoxaline1.2.3 When the Synthon Supplies C2 + C3 of the Quinoxaline1.2.3.1 Using a Dialdehyde (Glyoxal) or Related Synthon; 1.2.3.2 Using an Aldehydo Ketone or Related Synthon; 1.2.3.3 Using an Aldehydo Acid or Related Synthon; 1.2.3.4 Using an Aldehydo Ester or Related Synthon; 1.2.3.5 Using an Aldehydo Amide, Nitrile, Acyl Halide, or Related Synthon; 1.2.3.6 Using a Diketone or Related Synthon; 1.2.3.7 Using a Keto Acid or Related Synthon; 1.2.3.8 Using a Keto Ester or Related Synthon; 1.2.3.9 Using a Keto Amide, Nitrile, Acyl Halide, or Related Synthon1.2.3.10 Using a Diacid (Oxalic Acid) as Synthon1.2.3.11 Using a Diester (a Dialkyl Oxalate) or Related Synthon; 1.2.3.12 Using an Estero Amide, Nitrile, Acyl Halide, or Related Synthon; 1.2.3.13 Using a Diamide (Oxamide), Amido Nitrile, or Related Synthon; 1.2.3.14 Using a Diacyl Dihalide (Oxalyl Halide) or Related Synthon; 1.2.4 When the Synthon Supplies N1 + C2 + C3 of the Quinoxaline; 1.2.5 When the Synthon Supplies N1 + C2 + C3 + N4 of the Quinoxaline; 1.3 From a Benzene Substrate with Two or More Synthons; 1.4 From a Pyrazine Substrate with or without Synthon(s)1.5 From Other Heteromonocyclic Substrates/Synthons1.5.1 Azirines as Substrates/Synthons; 1.5.2 1,2,3-Dithiazol-1-iums as Substrates/Synthons; 1.5.3 Furans as Substrates/Synthons; 1.5.4 Isothiazoles as Substrates/Synthons; 1.5.5 Isoxazoles as Substrates/Synthons; 1.5.6 Oxazoles as Substrates/Synthons; 1.5.7 Oxirenes as Substrates/Synthons; 1.5.8 Pyrans as Substrates/Synthons; 1.5.9 Pyridazines as Substrates/Synthons; 1.5.10 Pyridines as Substrates/Synthons; 1.5.11 Pyrimidines as Substrates/Synthons; 1.5.12 Pyrroles as Substrates/Synthons; 1.5.13 Thiophenes as Substrates/Synthons1.5.14 1,2,4-Triazines as Substrates/Synthons1.5.15 1,2,3-Triazoles as Substrates/Synthons; 1.6 From Heterobicyclic Substrates/Synthons; 1.6.1 7-Azabicyclo[4.1.0]heptanes as Substrates/Synthons; 1.6.2 Benzimidazoles as Substrates/Synthons; 1.6.3 1,4-Benzodiazepines as Substrates/Synthons; 1.6.4 1,5-Benzodiazepines as Substrates/Synthons; 1.6.5 1-Benzopyrans (Chromenes) as Substrates/Synthons; 1.6.6 2,1,3-Benzoselena(or thia)diazoles as Substrates/Synthons; 1.6.7 2,1,3-Benzoxadiazoles as Substrates/Synthons; 1.6.8 Cycloheptapyrazines as Substrates/Synthons; 1.6.9 Indoles as Substrates/Synthons1.6.10 Pyrrolo[3,4-b]pyrazines as Substrates/SynthonsThis volume in the Chemistry of Heterocyclic Compounds series presents a comprehensive review of the quinoxaline literature from 1975 to the present (2002), updating Volumes 5 and 35. It provides an alphabetical table of known simple quinoxalines, including new compounds discussed in this volume and their physical data, as well as the pyrazines from the original volumes. Biological activities, spectral or other physical studies, and other such materials appear at appropriate points in the text. The in-depth coverage includes synthesis, reactions, spectroscopic, and physical properties for eachChemistry of heterocyclic compounds ;v. 61.QuinoxalinesQuinoxalines.547.593547/.59/05Brown D. J383088MiAaPQMiAaPQMiAaPQBOOK9911020447803321Quinoxalines4416514UNINA