Process for the preparation of unsymmetric bis(imino) compounds

Preparation of monoimine compound (I) comprises reacting dicarbonyl compound (II) with an aniline compound (III) in presence of an aliphatic, non-aromatic solvent. Preparation of monoimine compound of formula (I) comprises reacting dicarbonyl compound of formula (II) with an aniline compound of form...

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Hauptverfasser: BILDSTEIN, BENNO, MIHAN, SHAHRAM, SOLCHINGER, ALEXANDER, SCHLAWJINSKI, SASCHA, KOELLING, LARS
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MIHAN, SHAHRAM
SOLCHINGER, ALEXANDER
SCHLAWJINSKI, SASCHA
KOELLING, LARS
description Preparation of monoimine compound (I) comprises reacting dicarbonyl compound (II) with an aniline compound (III) in presence of an aliphatic, non-aromatic solvent. Preparation of monoimine compound of formula (I) comprises reacting dicarbonyl compound of formula (II) with an aniline compound of formula (III) in presence of an aliphatic, non-aromatic solvent. Either R 1>, R 2>H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, or 5-7 membered heterocycle containing at least one of N, P, O or S, where the organic residues are replaced by halo, NR 11>2, OR 11>or SiR 12>3; and R 3>-R 10>H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 11>2, OR 11>, halo, SiR 12>3or 5-7 membered heterocycle, which contains at least an atom of N, P, O or S, where the organic residue R 3>-R 10>can be replaced by halo, CN, NR 11>2, OR 11>or SiR 12>3; or 2(R 1>R 2>)+(R 3>-R 10>) : 5-7 membered heterocycle ring; or 2(R 3>-R 5>), 2(R 6>-R 10>) : 5-7 membered heterocycle ring containing at least one of N, P, O or S; either R 11>H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl or SiR 12>3, where the organic residue of R 11>can be replaced by halo; and R 12>H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl or arylalkyl with 1-10C alkyl, or 6-20C-aryl; or 2R 11>+R 12>5-6 membered ring; E 1>-E 3>C (preferred), N or P; and u : 0 (when E 1>-E 3>is N or P) or 1 (when E 1>-E 3>is C). Independent claims are included for: (1) a monoimine compound of formula (Ia); (2) asymmetrical bis(imino)compound of formula (IV); (3) asymmetrical iron complex compound of formula (V); (4) a catalyst system for olefin polymerization comprising at least an iron complex (V), optionally an organic or inorganic carrier, optionally one or more activator, optionally another olefin polymerization suitable catalyst and optionally one or more metal compound of the periodic table; (5) a prepolymerization catalyst system comprising a catalyst system and addition polymerization of one or more linear 2-10C-1-alkene in a density ratio of 1:0.1-1:1000; and (6) a procedure for the manufacture of polyolefin through polymerization or copolymerization of olefin in presence of a catalyst system. A : Cl, Br, I, CF 3or OR 11>; X : F, Cl, Br, I, H, 1-10C-alkyl, 2-10C-alkenyl, 6-20C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 18>2, OR 18>, SR 18>, SO 3R 18>, OC(O)R 18>, CN, SCN, beta -diketonate, CO, BF 4->, PF 6->
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fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_ZA200805967B</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ZA200805967B</sourcerecordid><originalsourceid>FETCH-epo_espacenet_ZA200805967B3</originalsourceid><addsrcrecordid>eNrjZLAPKMpPTi0uVkjLL1IoyUhVKChKLUgsSizJzM9TyE9TKM0rrszNTS0pykxWSMos1sjMzczL11RIzs8tyC_NSynmYWBNS8wpTuWF0twMim6uIc4euqkF-fGpxQWJyal5qSXxUY5GBgYWBqaWZuZOxsSoAQCwhDFK</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Process for the preparation of unsymmetric bis(imino) compounds</title><source>esp@cenet</source><creator>BILDSTEIN, BENNO ; MIHAN, SHAHRAM ; SOLCHINGER, ALEXANDER ; SCHLAWJINSKI, SASCHA ; KOELLING, LARS</creator><creatorcontrib>BILDSTEIN, BENNO ; MIHAN, SHAHRAM ; SOLCHINGER, ALEXANDER ; SCHLAWJINSKI, SASCHA ; KOELLING, LARS</creatorcontrib><description>Preparation of monoimine compound (I) comprises reacting dicarbonyl compound (II) with an aniline compound (III) in presence of an aliphatic, non-aromatic solvent. Preparation of monoimine compound of formula (I) comprises reacting dicarbonyl compound of formula (II) with an aniline compound of formula (III) in presence of an aliphatic, non-aromatic solvent. Either R 1&gt;, R 2&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, or 5-7 membered heterocycle containing at least one of N, P, O or S, where the organic residues are replaced by halo, NR 11&gt;2, OR 11&gt;or SiR 12&gt;3; and R 3&gt;-R 10&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 11&gt;2, OR 11&gt;, halo, SiR 12&gt;3or 5-7 membered heterocycle, which contains at least an atom of N, P, O or S, where the organic residue R 3&gt;-R 10&gt;can be replaced by halo, CN, NR 11&gt;2, OR 11&gt;or SiR 12&gt;3; or 2(R 1&gt;R 2&gt;)+(R 3&gt;-R 10&gt;) : 5-7 membered heterocycle ring; or 2(R 3&gt;-R 5&gt;), 2(R 6&gt;-R 10&gt;) : 5-7 membered heterocycle ring containing at least one of N, P, O or S; either R 11&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl or SiR 12&gt;3, where the organic residue of R 11&gt;can be replaced by halo; and R 12&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl or arylalkyl with 1-10C alkyl, or 6-20C-aryl; or 2R 11&gt;+R 12&gt;5-6 membered ring; E 1&gt;-E 3&gt;C (preferred), N or P; and u : 0 (when E 1&gt;-E 3&gt;is N or P) or 1 (when E 1&gt;-E 3&gt;is C). Independent claims are included for: (1) a monoimine compound of formula (Ia); (2) asymmetrical bis(imino)compound of formula (IV); (3) asymmetrical iron complex compound of formula (V); (4) a catalyst system for olefin polymerization comprising at least an iron complex (V), optionally an organic or inorganic carrier, optionally one or more activator, optionally another olefin polymerization suitable catalyst and optionally one or more metal compound of the periodic table; (5) a prepolymerization catalyst system comprising a catalyst system and addition polymerization of one or more linear 2-10C-1-alkene in a density ratio of 1:0.1-1:1000; and (6) a procedure for the manufacture of polyolefin through polymerization or copolymerization of olefin in presence of a catalyst system. A : Cl, Br, I, CF 3or OR 11&gt;; X : F, Cl, Br, I, H, 1-10C-alkyl, 2-10C-alkenyl, 6-20C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 18&gt;2, OR 18&gt;, SR 18&gt;, SO 3R 18&gt;, OC(O)R 18&gt;, CN, SCN, beta -diketonate, CO, BF 4-&gt;, PF 6-&gt;, or non coordinated anion; either R 18&gt;, R 19&gt;H, 1-20C-alkyl, 2-20C-alkenyl, 6-20C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, SiR 19&gt;3, where the organic residue can be replaced by halo, N and O; or 2(R 18&gt;), 2(R 19&gt;) : 5-7 membered ring; s : 1-4, preferably 2 or 3; D : neutral donor; and t : 0-4, preferably 0-2. [Image] [Image] [Image].</description><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; HETEROCYCLIC COMPOUNDS ; MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS ; METALLURGY ; ORGANIC CHEMISTRY ; ORGANIC MACROMOLECULAR COMPOUNDS ; PERFORMING OPERATIONS ; PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; THEIR RELEVANT APPARATUS ; TRANSPORTING</subject><creationdate>2009</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20090429&amp;DB=EPODOC&amp;CC=ZA&amp;NR=200805967B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20090429&amp;DB=EPODOC&amp;CC=ZA&amp;NR=200805967B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>BILDSTEIN, BENNO</creatorcontrib><creatorcontrib>MIHAN, SHAHRAM</creatorcontrib><creatorcontrib>SOLCHINGER, ALEXANDER</creatorcontrib><creatorcontrib>SCHLAWJINSKI, SASCHA</creatorcontrib><creatorcontrib>KOELLING, LARS</creatorcontrib><title>Process for the preparation of unsymmetric bis(imino) compounds</title><description>Preparation of monoimine compound (I) comprises reacting dicarbonyl compound (II) with an aniline compound (III) in presence of an aliphatic, non-aromatic solvent. Preparation of monoimine compound of formula (I) comprises reacting dicarbonyl compound of formula (II) with an aniline compound of formula (III) in presence of an aliphatic, non-aromatic solvent. Either R 1&gt;, R 2&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, or 5-7 membered heterocycle containing at least one of N, P, O or S, where the organic residues are replaced by halo, NR 11&gt;2, OR 11&gt;or SiR 12&gt;3; and R 3&gt;-R 10&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 11&gt;2, OR 11&gt;, halo, SiR 12&gt;3or 5-7 membered heterocycle, which contains at least an atom of N, P, O or S, where the organic residue R 3&gt;-R 10&gt;can be replaced by halo, CN, NR 11&gt;2, OR 11&gt;or SiR 12&gt;3; or 2(R 1&gt;R 2&gt;)+(R 3&gt;-R 10&gt;) : 5-7 membered heterocycle ring; or 2(R 3&gt;-R 5&gt;), 2(R 6&gt;-R 10&gt;) : 5-7 membered heterocycle ring containing at least one of N, P, O or S; either R 11&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl or SiR 12&gt;3, where the organic residue of R 11&gt;can be replaced by halo; and R 12&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl or arylalkyl with 1-10C alkyl, or 6-20C-aryl; or 2R 11&gt;+R 12&gt;5-6 membered ring; E 1&gt;-E 3&gt;C (preferred), N or P; and u : 0 (when E 1&gt;-E 3&gt;is N or P) or 1 (when E 1&gt;-E 3&gt;is C). Independent claims are included for: (1) a monoimine compound of formula (Ia); (2) asymmetrical bis(imino)compound of formula (IV); (3) asymmetrical iron complex compound of formula (V); (4) a catalyst system for olefin polymerization comprising at least an iron complex (V), optionally an organic or inorganic carrier, optionally one or more activator, optionally another olefin polymerization suitable catalyst and optionally one or more metal compound of the periodic table; (5) a prepolymerization catalyst system comprising a catalyst system and addition polymerization of one or more linear 2-10C-1-alkene in a density ratio of 1:0.1-1:1000; and (6) a procedure for the manufacture of polyolefin through polymerization or copolymerization of olefin in presence of a catalyst system. A : Cl, Br, I, CF 3or OR 11&gt;; X : F, Cl, Br, I, H, 1-10C-alkyl, 2-10C-alkenyl, 6-20C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 18&gt;2, OR 18&gt;, SR 18&gt;, SO 3R 18&gt;, OC(O)R 18&gt;, CN, SCN, beta -diketonate, CO, BF 4-&gt;, PF 6-&gt;, or non coordinated anion; either R 18&gt;, R 19&gt;H, 1-20C-alkyl, 2-20C-alkenyl, 6-20C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, SiR 19&gt;3, where the organic residue can be replaced by halo, N and O; or 2(R 18&gt;), 2(R 19&gt;) : 5-7 membered ring; s : 1-4, preferably 2 or 3; D : neutral donor; and t : 0-4, preferably 0-2. [Image] [Image] [Image].</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>PERFORMING OPERATIONS</subject><subject>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><subject>THEIR RELEVANT APPARATUS</subject><subject>TRANSPORTING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2009</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLAPKMpPTi0uVkjLL1IoyUhVKChKLUgsSizJzM9TyE9TKM0rrszNTS0pykxWSMos1sjMzczL11RIzs8tyC_NSynmYWBNS8wpTuWF0twMim6uIc4euqkF-fGpxQWJyal5qSXxUY5GBgYWBqaWZuZOxsSoAQCwhDFK</recordid><startdate>20090429</startdate><enddate>20090429</enddate><creator>BILDSTEIN, BENNO</creator><creator>MIHAN, SHAHRAM</creator><creator>SOLCHINGER, ALEXANDER</creator><creator>SCHLAWJINSKI, SASCHA</creator><creator>KOELLING, LARS</creator><scope>EVB</scope></search><sort><creationdate>20090429</creationdate><title>Process for the preparation of unsymmetric bis(imino) compounds</title><author>BILDSTEIN, BENNO ; MIHAN, SHAHRAM ; SOLCHINGER, ALEXANDER ; SCHLAWJINSKI, SASCHA ; KOELLING, LARS</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ZA200805967B3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2009</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>PERFORMING OPERATIONS</topic><topic>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><topic>THEIR RELEVANT APPARATUS</topic><topic>TRANSPORTING</topic><toplevel>online_resources</toplevel><creatorcontrib>BILDSTEIN, BENNO</creatorcontrib><creatorcontrib>MIHAN, SHAHRAM</creatorcontrib><creatorcontrib>SOLCHINGER, ALEXANDER</creatorcontrib><creatorcontrib>SCHLAWJINSKI, SASCHA</creatorcontrib><creatorcontrib>KOELLING, LARS</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>BILDSTEIN, BENNO</au><au>MIHAN, SHAHRAM</au><au>SOLCHINGER, ALEXANDER</au><au>SCHLAWJINSKI, SASCHA</au><au>KOELLING, LARS</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Process for the preparation of unsymmetric bis(imino) compounds</title><date>2009-04-29</date><risdate>2009</risdate><abstract>Preparation of monoimine compound (I) comprises reacting dicarbonyl compound (II) with an aniline compound (III) in presence of an aliphatic, non-aromatic solvent. Preparation of monoimine compound of formula (I) comprises reacting dicarbonyl compound of formula (II) with an aniline compound of formula (III) in presence of an aliphatic, non-aromatic solvent. Either R 1&gt;, R 2&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, or 5-7 membered heterocycle containing at least one of N, P, O or S, where the organic residues are replaced by halo, NR 11&gt;2, OR 11&gt;or SiR 12&gt;3; and R 3&gt;-R 10&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 11&gt;2, OR 11&gt;, halo, SiR 12&gt;3or 5-7 membered heterocycle, which contains at least an atom of N, P, O or S, where the organic residue R 3&gt;-R 10&gt;can be replaced by halo, CN, NR 11&gt;2, OR 11&gt;or SiR 12&gt;3; or 2(R 1&gt;R 2&gt;)+(R 3&gt;-R 10&gt;) : 5-7 membered heterocycle ring; or 2(R 3&gt;-R 5&gt;), 2(R 6&gt;-R 10&gt;) : 5-7 membered heterocycle ring containing at least one of N, P, O or S; either R 11&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl or SiR 12&gt;3, where the organic residue of R 11&gt;can be replaced by halo; and R 12&gt;H, 1-22C-alkyl, 2-22C-alkenyl, 6-22C-aryl or arylalkyl with 1-10C alkyl, or 6-20C-aryl; or 2R 11&gt;+R 12&gt;5-6 membered ring; E 1&gt;-E 3&gt;C (preferred), N or P; and u : 0 (when E 1&gt;-E 3&gt;is N or P) or 1 (when E 1&gt;-E 3&gt;is C). Independent claims are included for: (1) a monoimine compound of formula (Ia); (2) asymmetrical bis(imino)compound of formula (IV); (3) asymmetrical iron complex compound of formula (V); (4) a catalyst system for olefin polymerization comprising at least an iron complex (V), optionally an organic or inorganic carrier, optionally one or more activator, optionally another olefin polymerization suitable catalyst and optionally one or more metal compound of the periodic table; (5) a prepolymerization catalyst system comprising a catalyst system and addition polymerization of one or more linear 2-10C-1-alkene in a density ratio of 1:0.1-1:1000; and (6) a procedure for the manufacture of polyolefin through polymerization or copolymerization of olefin in presence of a catalyst system. A : Cl, Br, I, CF 3or OR 11&gt;; X : F, Cl, Br, I, H, 1-10C-alkyl, 2-10C-alkenyl, 6-20C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, NR 18&gt;2, OR 18&gt;, SR 18&gt;, SO 3R 18&gt;, OC(O)R 18&gt;, CN, SCN, beta -diketonate, CO, BF 4-&gt;, PF 6-&gt;, or non coordinated anion; either R 18&gt;, R 19&gt;H, 1-20C-alkyl, 2-20C-alkenyl, 6-20C-aryl, 1-10C-arylalkyl in alkyl residue, 6-20C-aryl, SiR 19&gt;3, where the organic residue can be replaced by halo, N and O; or 2(R 18&gt;), 2(R 19&gt;) : 5-7 membered ring; s : 1-4, preferably 2 or 3; D : neutral donor; and t : 0-4, preferably 0-2. [Image] [Image] [Image].</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY
CHEMISTRY
COMPOSITIONS BASED THEREON
HETEROCYCLIC COMPOUNDS
MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
PERFORMING OPERATIONS
PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
THEIR PREPARATION OR CHEMICAL WORKING-UP
THEIR RELEVANT APPARATUS
TRANSPORTING
title Process for the preparation of unsymmetric bis(imino) compounds
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