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Volumn 62, Issue 11, 1997, Pages 3772-3774

Chromium(II)-Mediated Reformatsky Reactions of Carboxylic Esters with Aldehydes

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EID: 0001648020     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961910v     Document Type: Article
Times cited : (43)

References (41)
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    • In contrast to more powerful reducing agents like samarium(II), chromium(II) does not reduce carbonyl groups or simple halides normally
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    • note
    • 3 is used.
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    • This implies differences to a suggested model for the reactive species in the Nozaki-Hiyama reaction: cf. Mulzer in ref 7a
    • This implies differences to a suggested model for the reactive species in the Nozaki-Hiyama reaction: cf. Mulzer in ref 7a.
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    • 10 the product ratio is approximately 4:2:1 (79% yield). Although this is an improvement to existing Reformatsky approaches, it appears not to be synthetically useful at this stage. Cf.: Matsumoto, T.; Hosoda, Y.; Mori, K.; Fukui, K. Bull. Chem. Soc. Jpn. 1972, 45, 3156.
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