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Volumn 63, Issue 2, 1998, Pages 222-223

N-Hydroxyphthalimide-Catalyzed Carboxylation of Polycyclic Alkanes with Carbon Monoxide in the Presence of Dioxygen

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EID: 0000074729     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9718556     Document Type: Article
Times cited : (52)

References (41)
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    • In a previous paper, we demonstrated that PINO is easily generated by exposing NHPI to molecular oxygen, (a) Ishii, Y.; Nakayama, K.; Takeno, M.; Sakaguchi, S.; Iwahama, T.; Nishiyama, Y. J. Org. Chem. 1995, 60, 3934. (b) Iwahama, T.; Sakaguchi, S.; Nishiyama, Y.; Ishii, Y. Tetrahedron Lett. 1995, 36, 6923. (c) Ishii, Y.; Kato, S.; Iwahama, T.; Sakaguchi, S. Tetrahedron Lett. 1996, 37, 4993. (d) Ishii, Y.; Iwahama, T.; Sakaguchi, S.; Nakayama, K.; Nishiyama, Y. J. Org. Chem. 1996, 61, 4520. (e) Ishii, Y. J. Mol. Catal. A: Chem. 1997, 123. (f) Yoshino, Y.; Hayashi, Y.; Iwahama, T.; Sakaguchi, S.; Ishii, Y. J. Org. Chem. 1997, 62, 6810.
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    • 2°-H was estimated from total yield of 2, 3, 5, and 7/total yield of 4 and 6
    • 2°-H was estimated from total yield of 2, 3, 5, and 7/total yield of 4 and 6.


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