ACS Publications. Most Trusted. Most Cited. Most Read
My Activity
CONTENT TYPES

Figure 1Loading Img

Reaction of Unsymmetrical Cycloalkanones and Hydrazoic Acid; Synthesis of d,l-Lysine1

Cite this: J. Am. Chem. Soc. 1951, 73, 7, 3087–3091
Publication Date (Print):July 1, 1951
https://doi.org/10.1021/ja01151a034
    ACS Legacy Archive

    Article Views

    238

    Altmetric

    -

    Citations

    LEARN ABOUT THESE METRICS
    Other access options

    Note: In lieu of an abstract, this is the article's first page.

    Free first page

    Read this article

    To access this article, please review the available access options below.

    Get instant access

    Purchase Access

    Read this article for 48 hours. Check out below using your ACS ID or as a guest.

    Recommended

    Access through Your Institution

    You may have access to this article through your institution.

    Your institution does not have access to this content. You can change your affiliated institution below.

    Cited By

    This article is cited by 22 publications.

    1. Alvaro Salvador González, Ramón Gómez Arrayás, Marta Rodríguez Rivero and Juan C. Carretero. Catalytic Asymmetric Vinylogous Mannich Reaction of N-(2-Thienyl)sulfonylimines. Organic Letters 2008, 10 (19) , 4335-4337. https://doi.org/10.1021/ol8019082
    2. Luisa Benati,, Daniele Nanni,, Corrado Sangiorgi, and, Piero Spagnolo. Radical Chain Reactions of α-Azido-β-keto Esters with Tributyltin Hydride. A Novel Entry to Amides and Lactams through Regiospecific Nitrogen Insertion. The Journal of Organic Chemistry 1999, 64 (21) , 7836-7841. https://doi.org/10.1021/jo990837g
    3. S.P. Thomas, M.D. Greenhalgh. 8.16 Heterogeneous Hydrogenation of CC and CC Bonds. 2014, 564-604. https://doi.org/10.1016/B978-0-08-097742-3.00818-1
    4. Aaron Wrobleski, Thomas C. Coombs, Chan Woo Huh, Sze‐Wan Li, Jeffrey Aubé. The Schmidt Reaction. 2012, 1-320. https://doi.org/10.1002/0471264180.or078.01
    5. . Beckmann Rearrangement and Beckmann Fragmentation. 2010, 288-295. https://doi.org/10.1002/9780470638859.conrr064
    6. Eric J. Kantorowski, Mark J. Kurth. Expansion to Seven-Membered Rings. Tetrahedron 2000, 56 (26) , 4317-4353. https://doi.org/10.1016/S0040-4020(00)00218-0
    7. V. Rogers, S. Mendonca, T. W. Packham, M. J. Davies. Synthetic approaches to diazabiphenylenes: Synthesis of the carbon-nitrogen skeleton Of 1,5-and 2,6-diazabiphenylene. Heterocyclic Communications 2000, 6 (2) https://doi.org/10.1515/HC.2000.6.2.133
    8. . Azepanones. 1997, 117-250. https://doi.org/10.1002/9780470187968.ch3
    9. Gary L. Grunewald, Vilas H. Dahanukar. Synthesis of 3‐alkyl‐8‐substituted‐ and 4‐hydroxy‐8‐substituted‐2,3,4,5‐tetrahydro‐1 H ‐2‐benzazepines. Journal of Heterocyclic Chemistry 1994, 31 (6) , 1609-1617. https://doi.org/10.1002/jhet.5570310656
    10. . The synthesis of lactones and lactams. 1993, 1-268. https://doi.org/10.1002/9780470772522.ch1
    11. Grant R. Krow. Nitrogen insertion reactions of bridged bicyclic ketones. Regioselective lactam formation. Tetrahedron 1981, 37 (7) , 1283-1307. https://doi.org/10.1016/S0040-4020(01)92445-7
    12. Henry C. Wormser, Hanley N. Abramson. New Compounds: Total Synthesis of dl-3a,4,6a-cis-4-(4-Carboxybutyl)-hexahydropyrrolo[3,4-d]imidazol-2-one Hydrochloride (dl-Azabiotin Hydrochloride). Journal of Pharmaceutical Sciences 1977, 66 (8) , 1208-1210. https://doi.org/10.1002/jps.2600660844
    13. Walter Lwowski, Siegfried Linke. Cyclisierung von Alkanoylnitrenen. Justus Liebigs Annalen der Chemie 1977, 1977 (1) , 8-19. https://doi.org/10.1002/jlac.197719770103
    14. D. V. Banthorpe. Rearrangements involving azido groups. 1971, 397-440. https://doi.org/10.1002/9780470771266.ch7
    15. Peter Rosenmund, Dieter Sauer, Wolfgang Trommer. Beiträge zur Chemie des Indols, II Beckmann‐und Schmidt‐Umlagerungen an einigen Indolketonen. Chemische Berichte 1970, 103 (2) , 496-509. https://doi.org/10.1002/cber.19701030219
    16. C.V. Greco, R.P. Gray. Selective ring expansion of Δ5,10-octalin-1,6-diones via the Schmidt reaction. Tetrahedron 1970, 26 (18) , 4329-4337. https://doi.org/10.1016/S0040-4020(01)93078-9
    17. Manfred Augustin. Synthese und Eigenschaften höherer Aminodicarbonsäuren. Zeitschrift für Chemie 1967, 7 (6) , 216-222. https://doi.org/10.1002/zfch.19670070603
    18. G. Lardelli, V. Lamberti, W. T. Weller, A. P. de Jonge. The synthesis of lactones. Part I: Saturated δ‐ and ϵ‐Lactones. Recueil des Travaux Chimiques des Pays-Bas 1967, 86 (5) , 481-503. https://doi.org/10.1002/recl.19670860503
    19. Gustav Ehrhart, Günther Seidl. Über Umsetzungen mit Phenylnatrium, III. Chemische Berichte 1964, 97 (7) , 1994-1998. https://doi.org/10.1002/cber.19640970730
    20. P.A.S. Smith, E.P. Antoniades. The interplay of steric and electronic factors affecting geometrical isomerism of diaryl ketimine derivatives. Tetrahedron 1960, 9 (3-4) , 210-229. https://doi.org/10.1016/0040-4020(60)80010-5
    21. M. Brenner, H. R. Rickenbacher. Eine einfache Synthese von L ‐Lysin. Helvetica Chimica Acta 1958, 41 (1) , 181-188. https://doi.org/10.1002/hlca.660410122
    22. H. J. Schmid, A. Hunger, K. Hoffmann. Sterische und elektrostatische Effekte in der Schmidt ‐Reaktion. Helvetica Chimica Acta 1956, 39 (2) , 607-618. https://doi.org/10.1002/hlca.19560390234

    Pair your accounts.

    Export articles to Mendeley

    Get article recommendations from ACS based on references in your Mendeley library.

    Pair your accounts.

    Export articles to Mendeley

    Get article recommendations from ACS based on references in your Mendeley library.

    You’ve supercharged your research process with ACS and Mendeley!

    STEP 1:
    Click to create an ACS ID

    Please note: If you switch to a different device, you may be asked to login again with only your ACS ID.

    Please note: If you switch to a different device, you may be asked to login again with only your ACS ID.

    Please note: If you switch to a different device, you may be asked to login again with only your ACS ID.

    MENDELEY PAIRING EXPIRED
    Your Mendeley pairing has expired. Please reconnect