LEADER 00798nam0-22003131i-450- 001 990003350050403321 005 20001010 010 $a0-582-55553-1 035 $a000335005 035 $aFED01000335005 035 $a(Aleph)000335005FED01 035 $a000335005 100 $a20001010d--------km-y0itay50------ba 101 0 $aita 105 $ay-------001yy 200 1 $aLONGMAN PRIMARY DICTIONARY 205 $a1? 210 $aGREAT BRITAIN$cLONGMAN$d1982 610 0 $aDizionari ed Enciclopedie 676 $a403 700 1$aSummers,$bDella$0132561 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990003350050403321 952 $a403 SUM$bLINGUE 1478$fDECLI 959 $aDECLI 996 $aLONGMAN PRIMARY DICTIONARY$9443148 997 $aUNINA DB $aING01 LEADER 02089oam 2200577I 450 001 9910711452503321 005 20210916114344.0 035 $a(CKB)5470000002483516 035 $a(OCoLC)1055553955 035 $a(EXLCZ)995470000002483516 100 $a20181003d2018 ua 0 101 0 $aeng 135 $aurcn||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aTritium deposition in precipitation in the continental United States,1953-2012 /$fby Robert L. Michel, Bryant C. Jurgens, and Megan B. Young ; National Water-Quality Program 210 1$aReston, Virginia :$cU.S. Department of the Interior, U.S. Geological Survey,$d2018. 215 $a1 online resource (iv, 11 pages) $ccolor illustrations, color maps 225 1 $aScientific investigations report ;$v2018-5086 320 $aIncludes bibliographical references (pages 9-11). 606 $aTritium 606 $aRadioactive tracers in water pollution research$zUnited States 606 $aPrecipitation (Meteorology)$zUnited States 606 $aPrecipitation (Meteorology)$2fast 606 $aRadioactive tracers in water pollution research$2fast 606 $aTritium$2fast 607 $aUnited States$2fast 608 $aOnline resources. 615 0$aTritium. 615 0$aRadioactive tracers in water pollution research 615 0$aPrecipitation (Meteorology) 615 7$aPrecipitation (Meteorology) 615 7$aRadioactive tracers in water pollution research. 615 7$aTritium. 700 $aMichel$b Robert L.$01382859 702 $aJurgens$b Bryant C. 702 $aYoung$b Megan B. 712 02$aGeological Survey (U.S.), 712 02$aNational Water-Quality Assessment Program (U.S.) 801 0$bGPO 801 1$bGPO 801 2$bMERUC 801 2$bOCLCF 801 2$bOCLCA 801 2$bOCLCQ 801 2$bGPO 906 $aBOOK 912 $a9910711452503321 996 $aTritium deposition in precipitation in the continental United States,1953-2012$93435521 997 $aUNINA LEADER 05647nam 2200709 450 001 9910821673803321 005 20230807214439.0 010 $a1-119-00642-2 010 $a1-119-00622-8 010 $a1-119-00632-5 035 $a(CKB)3710000000397660 035 $a(EBL)1895902 035 $a(SSID)ssj0001460052 035 $a(PQKBManifestationID)12562797 035 $a(PQKBTitleCode)TC0001460052 035 $a(PQKBWorkID)11465735 035 $a(PQKB)11732885 035 $a(MiAaPQ)EBC1895902 035 $a(DLC) 2014047257 035 $a(Au-PeEL)EBL1895902 035 $a(CaPaEBR)ebr11043787 035 $a(CaONFJC)MIL770114 035 $a(OCoLC)897510777 035 $a(EXLCZ)993710000000397660 100 $a20150509h20152015 uy 0 101 0 $aeng 135 $aurcnu|||||||| 181 $ctxt 182 $cc 183 $acr 200 00$aStereoselective multiple bond-forming transformations in organic synthesis /$fedited by Jean Rodriguez and Damien Bonne ; foreword by Dieter Enders ; contributors, Muriel Amatore [and thirty-nine others] 210 1$aHoboken, New Jersey :$cWiley,$d2015. 210 4$dİ2015 215 $a1 online resource (472 p.) 300 $aDescription based upon print version of record. 311 $a1-118-67271-2 320 $aIncludes bibliographical references at the end of each chapters and index. 327 $aCover; Title Page; Copyright; Contents; List of Contributors; Foreword; Preface; Chapter 1 Definitions and Classifications of MBFTs; 1.1 Introduction; 1.2 Definitions; 1.3 Conclusion and Outlook; References; Part I Stereoselective Synthesis of Heterocycles; Chapter 2 Five-Membered Heterocycles; 2.1 Introduction; 2.2 Monocyclic Targets; 2.2.1 1,3-Dipolar Cycloaddition; 2.2.2 Michael Addition-Initiated Domino Process; 2.2.3 Multicomponent Reactions; 2.2.4 Carbohalogenation Reactions; 2.2.5 Radical Processes; 2.3 Fused Polycyclic Targets; 2.3.1 Cycloaddition Reactions 327 $a2.3.2 Domino Cyclization Reactions 2.4 Bridged Polycyclic Targets; 2.5 Conclusion and Outlook; References; Chapter 3 Six-Membered Heterocycles; 3.1 Introduction; 3.2 Monocyclic Targets; 3.2.1 Nitrogen-Only Heterocycles; 3.2.2 Oxygen-Containing Heterocycles; 3.3 Fused Polycyclic Targets; 3.3.1 Nitrogen-Only Fused Polycyclic Targets; 3.3.2 Oxygen-Containing Fused Polycyclic Targets; 3.3.3 Sulfur-Containing Fused Polycyclic Targets; 3.4 Bridged Polycyclic Targets; 3.4.1 General Procedure for the Preparation of 2,6-DABCO-Derived Compounds 138; 3.5 Polycyclic Spiro Targets; 3.6 Summary and Outlook 327 $aReferences Chapter 4 Other Heterocycles; 4.1 Introduction; 4.2 Synthesis of Medium-Sized Monocyclic, Fused and Bridged Polycyclic Heterocycles; 4.2.1 Ring Synthesis by Ring Transformation via Rearrangements/Ring Expansions; 4.2.2 Ring Synthesis by Annulation; 4.3 Summary and Outlook; References; Part II Stereoselective Synthesis of Carbocycles; Chapter 5 Three- and Four-Membered Carbocycles; 5.1 Introduction; 5.2 Cyclopropane Derivatives; 5.2.1 Organocatalysis and Related Reactions [Michael-Initiated Ring-Closure (MIRC) Reactions]; 5.2.2 Organometallics and Metal Catalysis 327 $a5.2.3 Lewis Acid-Promoted Sequences 5.2.4 Pericyclic Domino Strategies; 5.2.5 Radical Domino Strategies; 5.3 Cyclobutane Derivatives; 5.3.1 Organocatalyzed Cyclobutanations; 5.3.2 Organometallics and Metal Catalysis; 5.3.3 Acid- or Base-Promoted Transformations; 5.3.4 Multicomponent Reactions (MCRs); 5.4 Summary and Outlook; References; Chapter 6 Five-Membered Carbocycles; 6.1 Introduction; 6.2 Monocyclic Targets; 6.2.1 Metal-Catalyzed Reactions; 6.2.2 Organocatalytic Reactions; 6.2.3 Miscellaneous Reactions; 6.3 Fused Polycyclic Targets; 6.3.1 Metal-Catalyzed Reactions 327 $a6.3.2 Organocatalytic Reactions 6.3.3 Lewis Acid-Catalyzed Reactions; 6.3.4 Miscellaneous Reactions; 6.4 Bridged Polycyclic Targets; 6.5 Conclusion and Outlook; References; Chapter 7 Stereoselective Synthesis of Six-Membered Carbocycles; 7.1 Introduction; 7.2 Metal-Catalyzed Stereoselective Multiple Bond-Forming Transformations; 7.2.1 Introduction; 7.2.2 Cycloadditions; 7.2.3 Metal-Catalyzed Cascades as Formal [2+2+2] Cycloadditions; 7.2.4 Metal-Catalyzed Cycloisomerization Cascades; 7.3 Enantioselective Organocatalyzed Synthesis of Six-Membered Rings 327 $a7.3.1 Organocatalyzed Miscellaneous Reactions 330 $aMake synthesis more green, efficient, and economical Stereoselective multiple bond-forming transformations (MBFTs), which use one synthetic operation to selectively create at least two chemical bonds, decrease the total number of steps and increase atom economy while maximizing structural complexity and the functional diversity. In consequence, they reduce the amount of waste, money, and negative environmental impact of chemical processes. Combining such an important research topic with green chemistry, this book helps chemists identify sustainable stereoselective MBFTs. Along with the discu 606 $aOrganic compounds$xSynthesis 606 $aStereochemistry 606 $aChemical reactions 615 0$aOrganic compounds$xSynthesis. 615 0$aStereochemistry. 615 0$aChemical reactions. 676 $a547.2 702 $aRodriguez$b Jean 702 $aBonne$b Damien$f1979- 702 $aEnders$b Dieter 702 $aAmatore$b Muriel 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910821673803321 996 $aStereoselective multiple bond-forming transformations in organic synthesis$94096432 997 $aUNINA