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1. |
Synthesis of Photoaffinity Labelling Analogues of the Peptide Hormone Bradykinin |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 621-627
Endre Laczko,
Emanuel Escher,
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摘要:
AbstractFourteen peptides, analogues of bradykinin and (des‐Arg9)bradykinin, have been synthesized by the solid‐phase method or have been obtained through chemical modification. In all these peptides an aromatic residue has been substituted by (4′‐NO2)Phe, (4′‐NH2)Phe, (4′‐N3)Phe or (4′‐NH2‐3′, 5′‐I2)Phe. These peptides will be used as photoaffinity labelling or affinity labelling probes fo
ISSN:0018-019X
DOI:10.1002/hlca.19810640302
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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2. |
On the Relation between One‐Bond Coupling Constants and the s‐Electron Density at the Nucleus |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 628-629
Terence N. Mitchell,
Mostafa El‐Behairy,
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摘要:
AbstractA comparison ofMössbauerisomer shifts and direct Sn, Sn‐coupling constants for a series of di‐ and polytin compounds indicates that the s‐electron density at the Sn‐atom has little influence on this
ISSN:0018-019X
DOI:10.1002/hlca.19810640303
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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3. |
Synthese und Charakterisierung der 8 isomeren, im Ring B mono‐ bzw. dihydroxylierten Royleanone |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 630-642
Heidi Meier,
Peter Rüedi,
Conrad Hans Eugster,
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摘要:
Synthesis and Characterization of the 8 Stereoisomeric Royleanones with One or Two Hydroxy Groups in Ring BThe partial syntheses of 6α, 7α‐dihydroxyroyleanone (6a), 6α, 7β‐dihydroxyroyleanone (7a) and 6β, 7β‐dihydroxyroyleanone (9a) are described. Thus, all in ring B mono‐ and dihydroxylated royleanones are now known (see [2–11]), being fully characterized by extensive spectroscopic, chiroptic and chromatographic (HPLC.) methods. An opening of the epoxyroyleanone11ayieldscis‐ andtrans‐diols together with their corresponding mono‐ and di‐O‐acetyl derivatives. We postulate a reversible addition of the acetate ion at C(8) of the quinone system, followed by a neighbouring group participat
ISSN:0018-019X
DOI:10.1002/hlca.19810640304
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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4. |
2‐Bis (dimethylamino)phosphinoyl‐1‐lithio‐1, 2, 3, 4‐tetrahydroisoquinoline. A highly nucleophilic d1‐reagent for the preparation of 1‐substituted tetrahydroisoquinolines |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 643-647
Dieter Seebach,
Masaaki Yoshifuji,
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摘要:
AbstractThe title compound4is generated from the phosphoric amide5in tetrahydrofuran with butyllithium. The lithium reagent4is stable at room temperature; its reactions with electrophiles furnish the products6–22,26,27, seeTable 1and theScheme. A second alkylation is also possible, see23–25. The cleavage to tetrahydroisoquinolines is accomplished in refluxing aqueous‐methanolic hydrochloric acid, seeTable 2. Phosphinoylation, lithiation, reaction with electrophiles and cleavage constitute an efficient sequence for 1‐alkylation of the isoquinoline
ISSN:0018-019X
DOI:10.1002/hlca.19810640305
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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5. |
Azidiniumsalze. 22. Mitteilung. über 3‐äthyl‐2‐tetrazo‐6‐X‐benzo[d]thiazoline und ihre Reaktivität: Ein Beitrag zur Chemie nucleophiler Carbene |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 648-656
Heinz Balli,
Heinrich Grüner,
Rudolf Maul,
Horst Schepp,
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摘要:
3‐Ethyl‐2‐tetrazo‐6‐X‐benzo[d]thiazolines and Their Reactivity: A Contribution to the Chemistry of Nucleophilic CarbenesThe synthesis of 3‐ethyl‐2‐tetrazo‐6‐X‐benzo[d]thiazolines3‐ a new class of azohomologous diazo compounds ‐ by addition of azide ions to azidinium salts4is described, their structure and some of their reactions are disscussed. The thermolysis of3atca.270Kin DMFA or THF generates nucleophilic carbenes1, whose trapping by electrophilic compounds such as3,4, diazonium salts, diazo compounds, methanol, sulfur and tetracyanoethylene could be studied. Direct dimerisation of1to2(without acid/base catalysis) could not be found, as demons
ISSN:0018-019X
DOI:10.1002/hlca.19810640306
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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6. |
Erratum |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 656-656
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ISSN:0018-019X
DOI:10.1002/hlca.19810640307
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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7. |
Enantiomer‐Selectivity for Phenylethylammonium Ion of Membranes Based on a Chiral Macrocyclic Polyether |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 657-661
Walter Bussmann,
Wilhelm Simon,
Urs Oesch,
Jean‐Marie Lehn,
Pierre Plumeré,
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摘要:
AbstractA chiral macrocyclic crown ether exhibits an enantiomer‐selectivity of 2.6 for α‐phenylethylammonium ion when incorporated in solvent polymeric membranes. The sequence of selectivity of these membranes clearly differs from that of lipophilicity for the different biogenic ammonium ions studied, indicating a significant structural contribu
ISSN:0018-019X
DOI:10.1002/hlca.19810640308
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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8. |
Anil‐Synthese. 24. Mitteilung.über die Herstellung von Styryl‐ und Stilbenyl‐Derivaten des 1H‐Benzotriazols |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 662-680
Adolf Emil Siegrist,
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摘要:
Preparation of Styryl and Stilbenyl Derivatives of 1H‐Benzotriazoles1‐(p‐Tolyl)‐substituted 1H‐benzotriazoles react with anils of aromatic aldehydes in the presence of dimethylformamide and potassium hydroxide to yield the corresponding 1‐(styr‐4′‐yl)‐1H‐benzotriazoles and 1‐(stilben‐4′‐yl)‐1H‐benzotriazoles, respectively (‘anil synthesis’). Further, under the same reaction conditions, theSchiff's bases derived fromp‐chloroaniline and 4‐(1′H‐benzotriazol‐1′‐yl)benzaldehydes give, withp‐tolyl‐substituted heterocycles, the corre
ISSN:0018-019X
DOI:10.1002/hlca.19810640309
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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9. |
Aromatization of 1‐Benzyltetrahydroisoquinolines: Racemization of (−)‐(S)‐(N‐nor)‐Reticuline |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 681-686
Peter Buchs,
Arnold Brossi,
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摘要:
AbstractAromatization in the series of optically active 1‐benzyltetrahydroisoquinolines has been accomplished with (—)‐(S)−(N‐nor)‐reticuline (1b) and analogs. Direct catalytic or chemical reduction of the isoquinoline4obtained could not be achieved in a practical way but4was converted into1in three steps (4 → 8 → 9 → 1), in 55% overall yield. PartialO‐methylation of the isoquinoline4gave the isoquinoline alkaloid palaudine (5), before papave
ISSN:0018-019X
DOI:10.1002/hlca.19810640310
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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10. |
Chirale elektrophile Synthesebausteine mit vier verschiedenen funktionellen Gruppen aus Weinsäure, 2, 3‐ und 3, 4‐Epoxy‐butandiolderivate in allen vier stereoisomeren Formen |
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Helvetica Chimica Acta,
Volume 64,
Issue 3,
1981,
Page 687-702
Ernst Hungerbühler,
Dieter Seebach,
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摘要:
Chiral Electrophilic Synthetic Building Blocks with Four Different Functional Groups from Tartaric Acid, 2, 3‐ and 3, 4‐Epoxy‐butanediol Derivatives in All Four Stereoisomeric FormsEfficient and simple procedures have been developed for the preparation of thethreo‐ anderythro‐3, 4‐epoxy‐1, 2‐butanediol derivatives3and8and of thecis‐ andtrans‐2, 3‐epoxy‐1, 4‐butanediol derivatives7and9in both enantiomeric forms from tartaric acid (seeScheme 2). These epoxides should prove versatile as alkylating reagents in syntheses of enantiomerically pure natural products and of physiol
ISSN:0018-019X
DOI:10.1002/hlca.19810640311
出版商:WILEY‐VCH Verlag GmbH
年代:1981
数据来源: WILEY
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