LEADER 01187nam a2200349 i 4500 001 991000748689707536 005 20020507173058.0 008 951026s1982 uk ||| | eng 020 $a0521280404 035 $ab10751907-39ule_inst 035 $aLE01301710$9ExL 040 $aDip.to Matematica$beng 082 0 $a511.322 084 $aAMS 03E 100 1 $aBeller, A.$054377 245 10$aCoding the universe /$cA. Beller, R. Jensen, P. Welch 260 $aCambridge :$bCambridge University Press,$cc1982 300 $a353 p. ;$c23 cm 490 0 $aLondon Mathematical Society lecture note series,$x0076-0552 ;$v47 500 $aBibliography: p. 347-348 500 $aIncludes indexes 650 0$aAxiomatic set theory 650 0$aSet theory 650 0$aSymbolic logic and mathematical 700 1 $aJensen, Ronald Bjorn 700 1 $aWelch, P. 907 $a.b10751907$b23-02-17$c28-06-02 912 $a991000748689707536 945 $aLE013 03E BEL11 (1982)$g1$i2013000038544$lle013$o-$pE0.00$q-$rl$s- $t0$u0$v0$w0$x0$y.i10844958$z28-06-02 996 $aCoding the universe$9345365 997 $aUNISALENTO 998 $ale013$b01-01-95$cm$da $e-$feng$guk $h0$i1 LEADER 00953nam a22002771i 4500 001 991000388149707536 005 20031217195317.0 008 040204s1988 it a||||||||||||||||ita 020 $a882210594X 035 $ab12608531-39ule_inst 035 $aARCHE-061573$9ExL 040 $aDip. SSC$bita$cA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l. 082 04$a303.66 245 03$aLa guerra /$csaggi: E. Beseghi ... [et al.] ; interventi: G. Celli ... 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Hopper 210 $aAmsterdam ;$aPhiladelphia $cJ. Benjamins$dc1998 215 $a1 online resource (308 p.) 225 1 $aTypological studies in language,$x0167-7373 ;$vv. 37 300 $aChiefly papers presented at a symposium held during the 28th annual meeting of the Societas Linguistica Europaea which was held Aug. 1995, Leiden, Netherlands. 311 $a1-55619-649-0 311 $a90-272-2935-X 320 $aIncludes bibliographical references and indexes. 327 $aTHE LIMITS OF GRAMMATICALIZATION; Editorial page; Title page; Copy right page; Table of contents; Introduction; Grammaticalization and language contact, constructions and positions; Grammaticalization and clause linkage strategies; Some remarks on analogy, reanalysis and grammaticalization; Testing the boundaries of grammaticalization; Discourse and pragmatic conditions of grammaticalization; The paradigm at the end of the universe; At the boundaries of grammaticalization; The grammaticalization of the left sentence boundary in Hittite 327 $aOn the relationships between grammaticalization and lexicalizationStructural scope expansion and grammaticalization; On the application of the notion of grammaticalization to West African Pidgin English; Language Index; Name Index; Subject Index 330 $aThe earliest use of the term "grammaticalization" was to refer to the process whereby lexical words of a language (such as English keep in "he keeps bees") become grammatical forms (such as the auxiliary in "he keeps looking at me"). Changes of this kind, which involve semantic fading and a downshift from a major to a minor category, have generally been agreed to come under the heading of grammaticalization. But other changes that equally contribute to new grammatical forms do not involve this kind of fading. In recent years, a debate has arisen over how to constrain the term theoretically. Is 410 0$aTypological studies in language ;$vv. 37. 606 $aGrammar, Comparative and general$xGrammaticalization$vCongresses 615 0$aGrammar, Comparative and general$xGrammaticalization 676 $a415 701 $aGiacalone Ramat$b Anna$f1937-$0158029 701 $aHopper$b Paul J$0158233 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910781724903321 996 $aThe limits of grammaticalization$93814172 997 $aUNINA LEADER 03881nam 2200769z- 450 001 9910367737103321 005 20210211 010 $a3-03921-949-9 035 $a(CKB)4100000010106346 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/42797 035 $a(oapen)doab42797 035 $a(EXLCZ)994100000010106346 100 $a20202102d2019 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aCatalyzed Synthesis of Natural Products 210 $cMDPI - Multidisciplinary Digital Publishing Institute$d2019 215 $a1 online resource (82 p.) 311 08$a3-03921-948-0 330 $aNatural products have been a source of inspiration for chemists and chemical biologists for many years, and have a special relevance in the chemical space. In recent years, several novel synthetic strategies have appeared, such as diversity-oriented synthesis (DOS), biological-oriented synthesis (BiOS), and function-oriented synthesis (FOS), for accessing complex and functionally diverse molecules. In this manner, the synthesis of natural products has evolved towards simpler and ecological methods using biotransformation, combinatorial chemistry, or organocatalysts. In this issue, Prof. Chojnacka shows demonstrates the use of immobilized lipases as catalysts to aid in the synthesis of phosphatidylcholine enriched with myristic acid. Profs. Vila and Pedro used catalysts derived from (S)-mandelic acid to achieve the catalytic enantioselective addition of dimethylzinc to isatins. Prof. Diez shows the possibility of the obtention of 7,8-carvone epoxides in a diastereoselective manner using proline, quinidine, and diphenylprolinol as organocatalysts. A cheap, simple, clean, and scalable method involves the use of deep eutectic mixtures as reaction media, and Profs. Alonso and Guillena describe the use of this methodology for the enantioselective, organocatalyzed ?-amination of 1,3-dicarbonyl compounds. Biotransformations have been one of the methodologies for more efficient synthesis of natural products. Prof. Wu transforms ergostane triterpenoid antcin K using Psychrobacillus sp. Ak 187. Finally, Prof. Kovayashi reviews the total synthesis and biological evaluation of phaeosphaerides. The reader, through this issue, could gain an idea of the new directions that the synthesis of natural products using catalysts will have in the years to come. 606 $aChemistry$2bicssc 610 $a?-amination 610 $a3-hydroxyoxindole 610 $aacidolysis 610 $aaminocatalysis 610 $aantcin K 610 $aanticancer 610 $aAntrodia cinnamomea 610 $aasymmetric catalysis 610 $aasymmetric organocatalysis 610 $abenzimidazole 610 $abiotransformation 610 $acarvone 610 $achiral ?-hydroxyamide 610 $adeep eutectic solvents 610 $aegg-yolk phosphatidylcholine 610 $aepoxidation 610 $aepoxide 610 $agreen chemistry 610 $aimmobilized lipases 610 $ainteresterification 610 $aisatin 610 $amandelamides 610 $amyristic acid 610 $an/a 610 $anatural products 610 $aorganocatalysis 610 $aphaeosphaeride A 610 $aphaeosphaeride B 610 $aproline 610 $aPsychrobacillus 610 $aSTAT3 610 $astructural revision 610 $astructured phosphatidylcholine 610 $atotal synthesis 610 $atrimyristin 610 $atriterpenoid 610 $azinc 615 7$aChemistry 700 $aDíez$b David$4auth$01304417 906 $aBOOK 912 $a9910367737103321 996 $aCatalyzed Synthesis of Natural Products$93027384 997 $aUNINA