DOI: 10.1002/cber.19610941032. Isonitrile, IX. α‐Addition von Immonium‐Ionen und Carbonsäure‐Anionen an Isonitrile

Isonitrile, IX. α‐Addition von Immonium‐Ionen und Carbonsäure‐Anionen an Isonitrile

10.1002/cber.19610941032

Crossref journal-article

Wiley

Chemische Berichte (311)

Abstract

AbstractAus Carbonsäuren, Ammoniak oder primären Aminen, Aldehyden bzw. Ketonen und Isonitrilen entstehen α‐Acylamino‐carbonsäure‐amide. Diese Reaktion gestattet es u. a., geschützte Oligopeptide und β‐Lactame einstufig aus einfachen Ausgangsmaterialien aufzubauen.

Bibliography

Ugi, I., & SteinbrÃ¼ckner, C. (1961). Isonitrile, IX. Î±âAddition von ImmoniumâIonen und CarbonsÃ¤ureâAnionen an Isonitrile. Chemische Berichte, 94(10), 2802â2814. Portico.

Authors 2

Ivar Ugi (first)
Cornelius Steinbrückner (additional)

References 31 Referenced 130

10.1002/cber.19610941031
10.1002/ange.19600720709
10.1002/cber.19610940323
(c) Sammelref.:I.Ugi Angew. Chem.(im Druck).
{'key': 'e_1_2_1_3_2', 'volume-title': 'α‐Aminoalkylierung', 'author': 'Hellmann H.', 'year': '1960'} / α‐Aminoalkylierung by Hellmann H. (1960)
{'key': 'e_1_2_1_4_2', 'first-page': '964', 'volume': '61', 'author': 'Passerini M.', 'year': '1931', 'journal-title': 'Gazz. chim. ital.'} / Gazz. chim. ital. by Passerini M. (1931)
10.1002/cber.19610940844
10.1002/cber.19610940845
Über analoge Synthesen auch höherer Oligopeptide und von Verbindungen mit mehreten Asymmetriezentren werdenI.UgiundK.Offermannin Bälde berichten.
10.1002/ange.19610731713
10.1039/qr9470100299
10.1021/ja01143a007
10.1002/hlca.19590420651
{'key': 'e_1_2_1_8_2', 'first-page': '388', 'volume-title': 'Org. Reactions', 'author': 'Sheehan J. S.', 'year': '1957'} / Org. Reactions by Sheehan J. S. (1957)
{'key': 'e_1_2_1_9_2', 'first-page': '75', 'volume-title': 'Methoden der organ. Chemie (Houben‐Weyl)', 'author': 'Petersen S.', 'year': '1952'} / Methoden der organ. Chemie (Houben‐Weyl) by Petersen S. (1952)
10.1002/cber.19150480154
10.1021/ja01548a059
10.1002/cber.19600930537
10.1021/ja01465a069
10.1002/cber.19600930136
10.1002/cber.19610941033
{'key': 'e_1_2_1_12_2', 'first-page': '886', 'volume-title': 'Chemistry of the Amino acids', 'author': 'Greenstein J. P.', 'year': '1961'} / Chemistry of the Amino acids by Greenstein J. P. (1961)
10.1021/ja01229a023
M. D.Hurwitz Amer. Pat. 2 582 128 [1950];
{'key': 'e_1_2_1_13_4', 'first-page': '8146f', 'volume': '46', 'year': '1952', 'journal-title': 'C. A.'} / C. A. (1952)
10.1021/jo01372a010
Diese Ergebnisse wurden der Redaktion am 15 6. 1961 eingereicht.
V o wird in 73‐proz. Ausbeute aus Chloressigsäure n‐Butylamin Cyclohexanon und Cyclohexyl‐isocyanid in Benzol erhalten.
Da Phthalyl‐glycin Isocyanessigsäure‐tert.‐tert.‐butylester Methylbenzylketon und Benzylamin unter den gewählten Bedingungen in 4 Wochen noch nicht ausreagiert hatten setzten wir statt der beiden letzten Komponenten Methylbenzylketon‐benzylimid ein.
10.1021/ja01293a033
10.1002/ange.19590711512

Dates

Type	When
Created	18 years, 3 months ago (June 3, 2007, 5:51 a.m.)
Deposited	1 year, 9 months ago (Nov. 23, 2023, 2:54 p.m.)
Indexed	3 weeks, 6 days ago (Aug. 7, 2025, 4:29 p.m.)
Issued	63 years, 11 months ago (Oct. 1, 1961)
Published	63 years, 11 months ago (Oct. 1, 1961)
Published Online	19 years, 7 months ago (Jan. 21, 2006)
Published Print	63 years, 11 months ago (Oct. 1, 1961)

Funders 0

None

BibTeX

@article{Ugi_1961, title={Isonitrile, IX. α‐Addition von Immonium‐Ionen und Carbonsäure‐Anionen an Isonitrile}, volume={94}, ISSN={0009-2940}, url={http://dx.doi.org/10.1002/cber.19610941032}, DOI={10.1002/cber.19610941032}, number={10}, journal={Chemische Berichte}, publisher={Wiley}, author={Ugi, Ivar and Steinbrückner, Cornelius}, year={1961}, month=oct, pages={2802–2814} }

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