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Mattingly, Phillip G., Kerwin, James F., Miller, Marvin J. (1979) A facile synthesis of substituted N-hydroxy-2-azetidinones. A biogenetic type .beta.-lactam synthesis. Journal Of The American Chemical Society, 101 (14) 3983-3985 doi:10.1021/ja00508a056

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Reference TypeJournal (article/letter/editorial)
TitleA facile synthesis of substituted N-hydroxy-2-azetidinones. A biogenetic type .beta.-lactam synthesis
JournalJournal Of The American Chemical Society
AuthorsMattingly, Phillip G.Author
Kerwin, James F.Author
Miller, Marvin J.Author
Year1979 (July)Volume101
Issue14
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00508a056Search in ResearchGate
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Mindat Ref. ID1354098Long-form Identifiermindat:1:5:1354098:2
GUID0
Full ReferenceMattingly, Phillip G., Kerwin, James F., Miller, Marvin J. (1979) A facile synthesis of substituted N-hydroxy-2-azetidinones. A biogenetic type .beta.-lactam synthesis. Journal Of The American Chemical Society, 101 (14) 3983-3985 doi:10.1021/ja00508a056
Plain TextMattingly, Phillip G., Kerwin, James F., Miller, Marvin J. (1979) A facile synthesis of substituted N-hydroxy-2-azetidinones. A biogenetic type .beta.-lactam synthesis. Journal Of The American Chemical Society, 101 (14) 3983-3985 doi:10.1021/ja00508a056
In(1979, July) Journal Of The American Chemical Society Vol. 101 (14) American Chemical Society (ACS)

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MATTINGLY, P. G., KERWIN, J. F. JUN., MILLER, M. J. (1979) ChemInform Abstract: A FACILE SYNTHESIS OF SUBSTITUTED N-HYDROXY-2-AZETIDINONES. A BIOGENETIC TYPE β-LACTAM SYNTHESIS. Chemischer Informationsdienst, 10 (43) doi:10.1002/chin.197943221
Miller, Marvin J., Mattingly, Phillip G., Morrison, Marjorie A., Kerwin, James F. (1980) Synthesis of .beta.-lactams from substituted hydroxamic acids. Journal Of The American Chemical Society, 102 (23) 7026-7032 doi:10.1021/ja00543a021
Miller, M., Mattingly, P., Morrison, M., Kerwin, Jr., J. (1981) Additions and Corrections - Synthesis of β-Lactams from Substituted Hydroxamic Acids. Journal Of The American Chemical Society, 103 (10) 2909 doi:10.1021/ja00400a601
Gasparski, Catherine M., Teng, Min, Miller, Marvin J. (1992) Functionalization of the .beta.-lactam ring: diastereoselective azide transfer and nitrogen-oxygen bond reduction on C4 substituted N-hydroxy-.beta.-lactams in one step. Journal Of The American Chemical Society, 114 (7) 2741-2743 doi:10.1021/ja00033a072
MATTINGLY, P. G., MILLER, M. J. (1980) ChemInform Abstract: TITANIUM TRICHLORIDE REDUCTION OF SUBSTITUTED N-HYDROXY-2-AZETIDINONES AND OTHER HYDROXAMIC ACIDS. Chemischer Informationsdienst, 11 (21) doi:10.1002/chin.198021128
MILLER, M. J., MATTINGLY, P. G., MORRISON, M. A., KERWIN, J. F. JUN. (1981) ChemInform Abstract: SYNTHESIS OF β-LACTAMS FROM SUBSTITUTED HYDROXAMIC ACIDS. Chemischer Informationsdienst, 12 (9) doi:10.1002/chin.198109216
Hecht, Sidney M., Rupprecht, Kathleen M., Jacobs, Paula M. (1979) Synthesis of L-erythro-.beta.-hydroxyhistidine from D-glucosamine. Journal Of The American Chemical Society, 101 (14) 3982-3983 doi:10.1021/ja00508a055
Nakatsuka, Shinichi, Tanino, Hideo, Kishi, Yoshito (1975) Biogenetic-type synthesis of penicillin-cephalosporin antibiotics. II. Oxidative cyclization route to .beta.-lactam thiazoline derivatives. Journal Of The American Chemical Society, 97 (17) 5010-5012 doi:10.1021/ja00850a043
Ernest, I., Gosteli, J., Woodward, R. B. (1979) The penems, a new class of .beta.-lactam antibiotics. 3. Synthesis of optically active 2-methyl-(5R)-penem-3-carboxylic acid. Journal Of The American Chemical Society, 101 (21) 6301-6305 doi:10.1021/ja00515a025
MATTINGLY, P. G., MILLER, M. J. (1981) ChemInform Abstract: SYNTHESIS OF 2-AZETIDINONES FROM SERINEHYDROXAMATES: APPROACHES TO THE SYNTHESIS OF 3-AMINONOCARDICINIC ACID. Chemischer Informationsdienst, 12 (38) doi:10.1002/chin.198138184
Lang, M., Prasad, K., Holick, W., Gosteli, J., Ernest, I., Woodward, R. B. (1979) The penems, a new class of .beta.-lactam antibiotics. 2. Total synthesis of racemic 6-unsubstituted representatives. Journal Of The American Chemical Society, 101 (21) 6296-6301 doi:10.1021/ja00515a024
 
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