MARC

LEADER 00000cam a2200000 i 4500
001 SCIDIR_ocn571245198
003 OCoLC
005 20231117033005.0
006 m o d
007 cr bn||||||abp
007 cr bn||||||ada
008 100325s1967 nyua ob 000 0 eng d
040 |a OCLCE  |b eng  |e rda  |e pn  |c OCLCE  |d OCLCQ  |d OPELS  |d OCLCQ  |d OCLCF  |d E7B  |d OCLCQ  |d LEAUB  |d LUN  |d OCLCQ  |d INARC  |d OCLCO  |d HNC  |d OCLCO  |d OCLCQ 
019 |a 297364617  |a 1145804391 
035 |a (OCoLC)571245198  |z (OCoLC)297364617  |z (OCoLC)1145804391 
042 |a dlr 
050 4 |a QD400  |b .H3 1967 
082 0 4 |a 547/.59 
084 |a 35.52  |2 bcl 
084 |a 35.59  |2 bcl 
084 |a VK 4000  |2 rvk 
084 |a VK 5500  |2 rvk 
084 |a 18.04  |2 bcl 
084 |a 35.51  |2 bcl 
100 1 |a Hamer, Jan. 
245 1 0 |a 1, 4-cycloaddition reactions  |b the Diels-Alder reaction in heterocyclic syntheses.  |c Edited by Jan Hamer. 
264 1 |a New York,  |b Academic Press,  |c 1967. 
300 |a 1 online resource (xii, 500 pages)  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Organic chemistry; a series of monographs,  |v v. 8 
504 |a Includes bibliographical references. 
505 0 |a Systems capable of 1,4-cycladdition reactions / Jan Hamer -- Formation of five-membered cyclic sulfones / S.D. Turk and R.L. Cobb -- Trivalent phosphorus compounds as dienophiles / Louis D. Quin -- Cyanogen and cyanogen-like compounds as dienophiles / G.J. Janz -- Imino compounds as dienophiles / Manuel Lora-Tamayo and R. Madronero -- Azo compounds as dienophiles / Bernard T. Gillis -- Dienes containing two nitrogen atoms in the conjugated system / Manuel Lora-Tamayo and Jose L. Soto -- Carbonyl and thiocarbonyl compounds as dienophiles / Jan Hamer and James A. Turner -- [Alpha], [beta]-unsaturated carbonyl compounds as dienes / J. Colonge and G. Descotes -- Oxygen as a dienophile / Klaus Gollnick and G�unther O. Schenck -- Cycloadditions to o-quinones, 1,2-diketones, and some of their derivatives / G. Pfundt and G.O. Schenck -- Nitroso compounds as dienophiles / Jan Homer and Mushtaq Ahmad -- N-sulfinyl compounds as dienophiles / G�unter Kresze. 
506 |3 Use copy  |f Restrictions unspecified  |2 star  |5 MiAaHDL 
533 |a Electronic reproduction.  |b [Place of publication not identified] :  |c HathiTrust Digital Library,  |d 2010.  |5 MiAaHDL 
538 |a Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002.  |u http://purl.oclc.org/DLF/benchrepro0212  |5 MiAaHDL 
583 1 |a digitized  |c 2010  |h HathiTrust Digital Library  |l committed to preserve  |2 pda  |5 MiAaHDL 
588 0 |a Print version record. 
650 0 |a Ring formation (Chemistry) 
650 0 |a Diels-Alder reaction. 
650 0 |a Heterocyclic compounds. 
650 2 |a Heterocyclic Compounds  |0 (DNLM)D006571 
650 2 |a Cyclization  |0 (DNLM)D003500 
650 6 |a Cyclisation (Chimie)  |0 (CaQQLa)201-0079127 
650 6 |a R�eaction de Diels-Alder.  |0 (CaQQLa)201-0019883 
650 6 |a Compos�es h�et�erocycliques.  |0 (CaQQLa)201-0006824 
650 7 |a 35.52 organic syntheses.  |0 (NL-LeOCL)077596013  |2 bcl 
650 7 |a 35.59 heterocyclic compounds.  |0 (NL-LeOCL)077596056  |2 bcl 
650 7 |a Diels-Alder reaction.  |2 fast  |0 (OCoLC)fst00893136 
650 7 |a Heterocyclic compounds.  |2 fast  |0 (OCoLC)fst00955736 
650 7 |a Ring formation (Chemistry)  |2 fast  |0 (OCoLC)fst01097987 
650 7 |a Chemische Synthese  |2 gnd  |0 (DE-588)4133806-6 
650 7 |a Cycloaddition  |2 gnd  |0 (DE-588)4148483-6 
650 7 |a Diels-Alder-Reaktion  |2 gnd  |0 (DE-588)4149746-6 
650 7 |a Heterocyclische Verbindungen  |2 gnd  |0 (DE-588)4159726-6 
650 1 7 |a Cycloadditie.  |2 gtt 
650 1 7 |a Synthese (chemie)  |2 gtt 
650 1 7 |a Diels-Alder-reacties.  |2 gtt 
650 1 7 |a Heterocyclische verbindingen.  |2 gtt 
776 0 8 |i Print version:  |a Hamer, Jan.  |t 1, 4-cycloaddition reactions.  |d New York, Academic Press, 1967  |w (DLC) 65026040  |w (OCoLC)544150 
830 0 |a Organic chemistry (New York, N.Y.) ;  |v v. 8. 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780123957436  |z Texto completo