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Volumn 70, Issue 1, 2005, Pages 334-337

Microwave- and photoirradiation-induced staudinger reactions of cyclic imines and ketenes generated from α-diazoketones. A further investigation into the stereochemical process

Author keywords

[No Author keywords available]

Indexed keywords

IRRADIATION; MICROWAVES; REACTION KINETICS; ULTRAVIOLET RADIATION;

EID: 12144267006     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo048328o     Document Type: Article
Times cited : (105)

References (30)
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    • For some recent reviews on β-lactam antibiotics, see: (a) Chemistry and Biology of β-Lactam Antibiotics; Morin, R. B., Gorman, M., Eds.; Academic Press: New York, 1982; Vols. 1-3. (b) Southgate, R.; Branch, C.; Coulton, S.; Hunt, E. In Recent Progress in the Chemical Synthesis of Antibiotics and Related Microbital Products; Luckacs, G., Ed.; Springer-Verlag; Berlin, 1993; Vol. 2, p 621. (c) Southgate, R. Contemp. Org. Synth. 1994, 1, 417.
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    • For photoirradiation-induced Staudinger reaction, see: (a) Podlech, J.; Linder, M. R. J. Org. Chem. 1997, 62, 5873-5883. (b) Linder, M. R.; Podlech, J. Org. Lett. 1999, 1, 869-871. (c) Maier, T. C.; Frey, W. U.; Podlech, J. Eur. J. Org. Chem. 2002, 2686-2689, (d) Linder, M. R.; Frey, W. U.; Podlech, J. J. Chem. Soc., Perkin Trans. 1 2001, 2566-2577.
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    • note
    • The following cyclic imines, including 2-cyclohexyl-1-pyrroline, 2-phenyl-1-pyrroline, 2-methyloxazoline, 2-phenyloxazoline, 2-(4-chlorophenyl) oxazoline, 5,6-dihydro-2-phenyl-4H-1,3-oxazine, and 2-phenylthiazoline, and α-diazoketones, such as 2-diazo-1-phenylethanone, 1-diazo-3-phenyl-2- propanone, were also attempted. However, no good result was obtained.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.