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Ulrich Schöllkopf (1927-1998)

Chemiker

Name	Ulrich Schöllkopf
Time	1927-1998 (Date of birth and death)
Place	Ebersbach an der Fils (Geburtsort) Göttingen (Sterbeort) Tübingen (Wirkungsort) Los Angeles, Calif. (Wirkungsort) Heidelberg (Wirkungsort) Göttingen (Wirkungsort) Deutschland
Academic degree	Dr. sc. nat. habil.
Profession	Chemiker (characteristic profession) Hochschullehrer
Topic	Personen zu Chemie
Further information	Nach Kriegsteilnahme als Luftwaffenhelfer und Kriegsgefangenschaft seit 1948 Chemiestudium in Tübingen, seit 1953 bei Georg Wittig (Nobelpreisträger 1979); 1956 Promotion; anschließend an der University of California in Los Angeles bei Donald Cram; 1961 Habilitation in Heidelberg; 1964 a.o., 1968 o. Professor für Organische Chemie in Göttingen; seit 1976 o. Mitglied der Akademie der Wissenschaften zu Göttingen; 1984 Liebig-Denkmünze der Gesellschaft Deutscher Chemiker; 1981 entwickelte er das Bislactimether-Verfahren, auch Schöllkopf-Methode oder Schöllkopf-Hartwig-Reaktion genannt
Source	Landesbibliographie Baden-Württemberg Internet
Record type	Person
GND-Identifier	124017991
Record ID	124017991
Involved in show all A New Route from Dihydroisoquinolines to 2-Benzazepines Asymmetric syntheses via heterocyclic intermediates (XIX) : on the enantioselective synthesis of alpha-Amino-beta-fluorocarboxylic esters Asymmetric syntheses via heterocyclic intermediates (XVII) : Enantioselective synthesis of (R)-alpha-methyl-S-benzylcysteine methyl ester and (R)-alpha-methyl-S-t-butylcysteine methyl ester using L-valine as chiralauxiliary reagent Asymmetric syntheses via heterocyclic intermediates. 22. Enantioselective synthesis of alpha-alkenyl glycine methyl esters and alphy-alkenyl glycines (beta,gamma-unsaturated amino acids) Asymmetric Synthesis of (+)-(1R,2S)-allo-Coronamic Acid Asymmetric Synthesis of Alpha-Amino Acid Benzyl Esters via the Bisbenzyl Bislactim Ether of cyclo(-L-Val-Gly-) Asymmetric Synthesis of D-erythro-Sphingosine Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3-Substituted (2R,3S)-Serine Methyl Esters Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure Alpha-Amino-Gamma-Nitro Carboxylic Esters via Michael Addition of the Titanated Bislactim Ether of Cyclo (-L-Val-Gly-) to Nitroolefines Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure, 3-Substituted (2S,3R)-N-Methylserine Esters Asymmetric Synthesis of Enantiomerically Pure Phosphonic Analogues of Glutamic Acid and Proline Asymmetric Synthesis of Methyl (2R,3S)-2-Amino-3-cyclopropyl-3-hydroxyalkanoates via Diastereoselective Simmons-Smith Reactions Asymmetric Synthesis via Heterocyclic Intermediates, LII. Synthesis of tert-Leucine and Related Amino Acids Asymmetrie synthess via heterocyclic intermediates (XV): enantioselective synthesis of (R)-(-)-beta-hydroxyvaline using L-valine or (S)-O,O-dimethyl-alpha-methyldopa as chiral auxiliary reagents Enantioselective synthesis of (R)-(-)-alpha-methylserine Enantioselektive Synthese von (2R)-2-Methylserinen Enantioselektive Synthese von (R)-Aminosauren unter Verwendung von L-Valin als chiralem Hilfsstoff Enantioselektive Synthese von alpha-Methyl-alpha-amino-carbonsäuren durch Alkylierung des Alkylierung des Lactimethers von cyclo-(L-Ala-L-Ala) Enantioselektive Synthese von alpha-Methylserinen Synthesis of Diastereomerically Pure 1-Aminocyclopropylphosphonic Acids Synthesis of Enantiomerically Pure Diethyl 2-Pyrrolidinyl- and 5-0xo-2-pyrrolidinylphosphonates Synthesis of Substituted Dibenzo[a,d]azepines via a Base-Mediated Ring Expansion Zur enantioselektiven Synthese von (2R)-Serin-methylestern oder (2R)-Serinen ausgehend vom Bislactimether von cyclo-(-L-Val-Gly-) Asymmetric Synthesis via Heterocyclic Intermediates, LII. Synthesis of tert ‐Leucine and Related Amino Acids Asymmetric Syntheses via Heterocyclic Intermediates, XLV. Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3‐Substituted (2 R, 3 S)‐serine Methyl Esters Asymmetrische Synthesen über heterocyclische Zwischenstufen, XVI. Enantioselektive Synthese von α‐Alkyl‐α‐phenylglycinen durch Alkylieren von an C‐6 chiral substituierten 3,6‐Dihydro‐3‐phenyl‐2 H ‐1,4‐oxazin‐2‐onen Asymmetric Syntheses via Heterocyclic Intermediates, XI. Enantioselective Synthesis of (R)‐(—)‐α‐Methylserine Asymmetrische Synthesen über heterocyclische Zwischenstufen, X. Enantioselektive Synthese von (2 R)‐2‐Methylserinen Enantioselektive Synthese von (R) ‐Aminosäuren unter Verwendung von L‐Valin als chiralem Hilfsstoff † ‡ Enantioselektive Synthese von α‐Methylserinen † ‡ Lactidkontraktion, eine Methode zur Synthese von α, α′‐ Dihydroxyketonen aus α‐Hydroxycarbonsäuren † Asymmetric Synthesis of α‐Amino‐γ‐nitrocarboxylic Esters by the Bislactim Ether Method † ‡ Enantioselective Syntheses of (R)‐Amino Acids Using l ‐Valine as Chiral Agent † ‡ Lactide Contraction—A Method for the Synthesis of α,α′‐Dihydroxy Ketones from α‐Hydroxy Carboxylic Acids † Asymmetric Synthesis via Heterocyclic Intermediates; XXIV1. Asymmetric Synthesis of Enantiomerically and Diastereomerically Pure D-Threonine by the Bis-lactim Ether Method Asymmetric Syntheses via Heterocyclic Intermediates; XV1. Enantioselective Synthesis of (R)-(-)-β-Hydroxyvaline using L,-Valine or (S)-O,O-Dimethyl-α-methyldopa as Chiral Auxiliary Reagents Asymmetric Syntheses via Heterocyclic Intermediates; XIX1. On the Enantioselective Synthesis of β-Fluorovaline Methyl Ester and Related α-Amino-β-fluorocarboxylic Esters Asymmetric Syntheses via Heterocyclic Intermediates; XIV1. Enantioselective Synthesis of (R)-Serine using L-Valine or O,O-Dimethyl-α-methyldopa as Chiral Auxiliary Reagents (Stereochemie und Reaktionsmechanismus der intra-anionischen Ätherisomerisation.) Über Triphenyl-phosphin-methylene als olefinbildende Reagenzien

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Katalog der Deutschen Nationalbibliothek

Ulrich Schöllkopf (1927-1998)

A New Route from Dihydroisoquinolines to 2-Benzazepines

Asymmetric syntheses via heterocyclic intermediates (XIX) : on the enantioselective synthesis of alpha-Amino-beta-fluorocarboxylic esters

Asymmetric syntheses via heterocyclic intermediates (XVII) : Enantioselective synthesis of (R)-alpha-methyl-S-benzylcysteine methyl ester and (R)-alpha-methyl-S-t-butylcysteine methyl ester using L-valine as chiralauxiliary reagent

Asymmetric syntheses via heterocyclic intermediates. 22. Enantioselective synthesis of alpha-alkenyl glycine methyl esters and alphy-alkenyl glycines (beta,gamma-unsaturated amino acids)

Asymmetric Synthesis of (+)-(1R,2S)-allo-Coronamic Acid

Asymmetric Synthesis of Alpha-Amino Acid Benzyl Esters via the Bisbenzyl Bislactim Ether of cyclo(-L-Val-Gly-)

Asymmetric Synthesis of D-erythro-Sphingosine

Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3-Substituted (2R,3S)-Serine Methyl Esters

Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure Alpha-Amino-Gamma-Nitro Carboxylic Esters via Michael Addition of the Titanated Bislactim Ether of Cyclo (-L-Val-Gly-) to Nitroolefines

Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure, 3-Substituted (2S,3R)-N-Methylserine Esters

Asymmetric Synthesis of Enantiomerically Pure Phosphonic Analogues of Glutamic Acid and Proline

Asymmetric Synthesis of Methyl (2R,3S)-2-Amino-3-cyclopropyl-3-hydroxyalkanoates via Diastereoselective Simmons-Smith Reactions

Asymmetric Synthesis via Heterocyclic Intermediates, LII. Synthesis of tert-Leucine and Related Amino Acids

Asymmetrie synthess via heterocyclic intermediates (XV): enantioselective synthesis of (R)-(-)-beta-hydroxyvaline using L-valine or (S)-O,O-dimethyl-alpha-methyldopa as chiral auxiliary reagents

Enantioselective synthesis of (R)-(-)-alpha-methylserine

Enantioselektive Synthese von (2R)-2-Methylserinen

Enantioselektive Synthese von (R)-Aminosauren unter Verwendung von L-Valin als chiralem Hilfsstoff

Enantioselektive Synthese von alpha-Methyl-alpha-amino-carbonsäuren durch Alkylierung des Alkylierung des Lactimethers von cyclo-(L-Ala-L-Ala)

Enantioselektive Synthese von alpha-Methylserinen

Synthesis of Diastereomerically Pure 1-Aminocyclopropylphosphonic Acids

Synthesis of Enantiomerically Pure Diethyl 2-Pyrrolidinyl- and 5-0xo-2-pyrrolidinylphosphonates

Synthesis of Substituted Dibenzo[a,d]azepines via a Base-Mediated Ring Expansion

Zur enantioselektiven Synthese von (2R)-Serin-methylestern oder (2R)-Serinen ausgehend vom Bislactimether von cyclo-(-L-Val-Gly-)

Asymmetric Synthesis via Heterocyclic Intermediates, LII. Synthesis of tert ‐Leucine and Related Amino Acids

Asymmetric Syntheses via Heterocyclic Intermediates, XLV. Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3‐Substituted (2 R, 3 S)‐serine Methyl Esters

Asymmetrische Synthesen über heterocyclische Zwischenstufen, XVI. Enantioselektive Synthese von α‐Alkyl‐α‐phenylglycinen durch Alkylieren von an C‐6 chiral substituierten 3,6‐Dihydro‐3‐phenyl‐2 H ‐1,4‐oxazin‐2‐onen

Asymmetric Syntheses via Heterocyclic Intermediates, XI. Enantioselective Synthesis of (R)‐(—)‐α‐Methylserine

Asymmetrische Synthesen über heterocyclische Zwischenstufen, X. Enantioselektive Synthese von (2 R)‐2‐Methylserinen

Enantioselektive Synthese von (R) ‐Aminosäuren unter Verwendung von L‐Valin als chiralem Hilfsstoff † ‡

Enantioselektive Synthese von α‐Methylserinen † ‡

Lactidkontraktion, eine Methode zur Synthese von α, α′‐ Dihydroxyketonen aus α‐Hydroxycarbonsäuren †

Asymmetric Synthesis of α‐Amino‐γ‐nitrocarboxylic Esters by the Bislactim Ether Method † ‡

Enantioselective Syntheses of (R)‐Amino Acids Using l ‐Valine as Chiral Agent † ‡

Lactide Contraction—A Method for the Synthesis of α,α′‐Dihydroxy Ketones from α‐Hydroxy Carboxylic Acids †

Asymmetric Synthesis via Heterocyclic Intermediates; XXIV1. Asymmetric Synthesis of Enantiomerically and Diastereomerically Pure D-Threonine by the Bis-lactim Ether Method

Asymmetric Syntheses via Heterocyclic Intermediates; XV1. Enantioselective Synthesis of (R)-(-)-β-Hydroxyvaline using L,-Valine or (S)-O,O-Dimethyl-α-methyldopa as Chiral Auxiliary Reagents

Asymmetric Syntheses via Heterocyclic Intermediates; XIX1. On the Enantioselective Synthesis of β-Fluorovaline Methyl Ester and Related α-Amino-β-fluorocarboxylic Esters

Asymmetric Syntheses via Heterocyclic Intermediates; XIV1. Enantioselective Synthesis of (R)-Serine using L-Valine or O,O-Dimethyl-α-methyldopa as Chiral Auxiliary Reagents

(Stereochemie und Reaktionsmechanismus der intra-anionischen Ätherisomerisation.)

Über Triphenyl-phosphin-methylene als olefinbildende Reagenzien