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Liebigs Annalen der Chemie

紙デジタル雑誌

VCH<Z53-B14>

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Pheromone Synthesis, CLXVII. Synthesis of All of the Eight Stereoisomers of Methyl 2,6,10‐Trimethyltridecanoate, the Male‐Produced Pheromone of the Stink Bugs, Euschistus heros and E. obscurus

デジタル記事

1994-11-30Liebigs Annalen der Chemie1994 12p.1153-1160

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掲載誌（ISSN）01702041 http://id.crossref.org/issn/01702041

Biologically Active Metabolites from Fungi, 5. Palmarumycins C1–C16 from Coniothyrium sp.: Isolation, Structure Elucidation, and Biological Activity

デジタル記事

1994-10-28Liebigs Annalen der Chemie1994 11p.1099-1108

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掲載誌（ISSN）01702041

Biologically Active Metabolites from Fungi, 4. Palmarumycins CP1–CP4 from Coniothyrium palmarum: Isolation, Structure Elucidation, and Biological Activity

デジタル記事

1994-10-28Liebigs Annalen der Chemie1994 11p.1093-1097

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掲載誌（ISSN）01702041

Caffeic Acid Glycoside Esters from Gratiola officinalis L.

デジタル記事

1994-10-28Liebigs Annalen der Chemie1994 11p.1113-1115

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掲載誌（ISSN）01702041

Aminosäuren, 18. Darstellung und Reaktionen von 2‐Isocyanato‐2‐alkensäureestern

デジタル記事

1994-10-28Liebigs Annalen der Chemie1994 11p.1069-1074

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掲載誌（ISSN）01702041

Total Synthesis of Angucyclines, 4. Synthesis of rac‐Tetrangomycin

デジタル記事

1994-10-28Liebigs Annalen der Chemie1994 11p.1109-1112

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掲載誌（ISSN）01702041

Chemical Interactions of Thiosemicarbazides with 1,4‐Benzo‐ and 1,4‐Naphthoquinones

デジタル記事

1994-09-30Liebigs Annalen der Chemie1994 10p.989-992

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掲載誌（ISSN）01702041

Stereoselective Amidoalkylation Reactions via N,O‐Acetals

デジタル記事

1994-09-02Liebigs Annalen der Chemie1994 9p.931-942

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掲載誌（ISSN）01702041

Derivate der Ketipinsäure, II. Ketipinsäuredilacton und verwandte Verbindungen

デジタル記事

1994-09-02Liebigs Annalen der Chemie1994 9p.961-964

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掲載誌（ISSN）01702041

TMS Triflate‐Promoted O‐Glycosylation of Amino Acids and Peptides by <scp>L</scp>‐Acosaminal and <scp>L</scp>‐Ristosaminal

デジタル記事

1994-08-05Liebigs Annalen der Chemie1994 8p.811-816

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掲載誌（ISSN）01702041

Stereocontrolled Synthesis of the Sex Pheromone of Nezara viridula (L.)

デジタル記事

1994-08-05Liebigs Annalen der Chemie1994 8p.785-789

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掲載誌（ISSN）01702041

Synthetic Microbial Chemistry, XXVI. Absolute Configuration of (+)‐Xanthocidin as Determined by the Synthesis of its Enantiomers of Known Stereochemistry

デジタル記事

1994-08-05Liebigs Annalen der Chemie1994 8p.817-825

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掲載誌（ISSN）01702041

Glycosyl Imidates, 66. Synthesis of the Tetrasaccharide Moiety of Plant Growth Regulator Calonyctin A

デジタル記事

1994-07-12Liebigs Annalen der Chemie1994 7p.645-651

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掲載誌（ISSN）01702041

Constituents of Holothuroideae, V. Isolation and Structure of Cerebrosides from the Sea Cucumber Pentacta australis

デジタル記事

1994-07-12Liebigs Annalen der Chemie1994 7p.653-658

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掲載誌（ISSN）01702041 http://id.crossref.org/issn/01702041

Dioxirane Oxidation of Furocoumarins and Naphthofurans Preparation of the Psoralen Epoxides

デジタル記事

1994-07-12Liebigs Annalen der Chemie1994 7p.689-693

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掲載誌（ISSN）01702041 http://id.crossref.org/issn/01702041

Total Synthesis of Myxovirescins, 2 Assembly of the “Northwestern” Part [C(15)–C(28)]

デジタル記事

1994-07-12Liebigs Annalen der Chemie1994 7p.719-729

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掲載誌（ISSN）01702041

Aborycin – A Tricyclic 21‐Peptide Antibiotic Isolated from Streptomyces griseoflavus

デジタル記事

1994-07-12Liebigs Annalen der Chemie1994 7p.741-743

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掲載誌（ISSN）01702041

Pheromone Synthesis, CLXIII. Synthesis of (9Z,25S,26R,43Z)‐25,26‐Epoxy‐9,43‐henpentacontadiene and Its Antipode, Components of the Nymph Recognition Pheromone Produced by Nymphs of the Cockroach Nauphoeta cinerea

デジタル記事

1994-07-12Liebigs Annalen der Chemie1994 7p.695-700

全国の図書館

掲載誌（ISSN）01702041

Total Syntheses, Optical Rotations and Fragrance Properties of Sandalwood Constituents: (−)‐(Z)‐ and (−)‐(E)‐β‐Santalol and Their Enantiomers, ent‐β‐Santalene

デジタル記事

1994-06-13Liebigs Annalen der Chemie1994 6p.601-609

全国の図書館

掲載誌（ISSN）01702041

検索結果 536 件

Liebigs Annalen der Chemie

Pheromone Synthesis, CLXVII. Synthesis of All of the Eight Stereoisomers of Methyl 2,6,10‐Trimethyltridecanoate, the Male‐Produced Pheromone of the Stink Bugs, <i>Euschistus heros</i> and <i>E. obscurus</i>

Biologically Active Metabolites from Fungi, 5. Palmarumycins C<sub>1</sub>–C<sub>16</sub> from <i>Coniothyrium</i> sp.: Isolation, Structure Elucidation, and Biological Activity

Biologically Active Metabolites from Fungi, 4. Palmarumycins CP<sub>1</sub>–CP<sub>4</sub> from <i>Coniothyrium palmarum</i>: Isolation, Structure Elucidation, and Biological Activity

Caffeic Acid Glycoside Esters from <i>Gratiola officinalis</i> L.

Aminosäuren, 18. Darstellung und Reaktionen von 2‐Isocyanato‐2‐alkensäureestern

Total Synthesis of Angucyclines, 4. Synthesis of <i>rac</i>‐Tetrangomycin

Chemical Interactions of Thiosemicarbazides with 1,4‐Benzo‐ and 1,4‐Naphthoquinones

Stereoselective Amidoalkylation Reactions via N,O‐Acetals

Derivate der Ketipinsäure, II. Ketipinsäuredilacton und verwandte Verbindungen

TMS Triflate‐Promoted <i>O</i>‐Glycosylation of Amino Acids and Peptides by <scp>L</scp>‐Acosaminal and <scp>L</scp>‐Ristosaminal

Stereocontrolled Synthesis of the Sex Pheromone of <i>Nezara viridula</i> (L.)

Synthetic Microbial Chemistry, XXVI. Absolute Configuration of (+)‐Xanthocidin as Determined by the Synthesis of its Enantiomers of Known Stereochemistry

Glycosyl Imidates, 66. Synthesis of the Tetrasaccharide Moiety of Plant Growth Regulator Calonyctin A

Constituents of Holothuroideae, V. Isolation and Structure of Cerebrosides from the Sea Cucumber <i>Pentacta australis</i>

Dioxirane Oxidation of Furocoumarins and Naphthofurans Preparation of the Psoralen Epoxides

Total Synthesis of Myxovirescins, 2 Assembly of the “Northwestern” Part [C(15)–C(28)]

Aborycin – A Tricyclic 21‐Peptide Antibiotic Isolated from <i>Streptomyces griseoflavus</i>

Pheromone Synthesis, CLXIII. Synthesis of (9<i>Z</i>,25<i>S</i>,26<i>R</i>,43<i>Z</i>)‐25,26‐Epoxy‐9,43‐henpentacontadiene and Its Antipode, Components of the Nymph Recognition Pheromone Produced by Nymphs of the Cockroach <i>Nauphoeta cinerea</i>

Total Syntheses, Optical Rotations and Fragrance Properties of Sandalwood Constituents: (−)‐(<i>Z</i>)‐ and (−)‐(<i>E</i>)‐β‐Santalol and Their Enantiomers, <i>ent</i>‐β‐Santalene