O-allylic substitution of hydroxylamine derivatives having an N-electron-withdrawing substituent

Synlett

Volumn , Issue 4, 2003, Pages 567-569

  Miyabe, Hideto ^a   Yoshida, Kazumasa ^a   Matsumura, Akira ^a   Yamauchi, Masashige ^b   Takemoto, Yoshiji ^a  

^a KYOTO UNIVERSITY   (Japan)

^b JOSAI UNIVERSITY   (Japan)

Author keywords

Allylations; Cyclizations; Iridium; Metathesis; Palladium

Indexed keywords

ALLYL COMPOUND; HYDROXYLAMINE; IRIDIUM COMPLEX; PALLADIUM COMPLEX;

ALLYLATION; ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; CYCLIZATION; ELECTRON TRANSPORT; RING CLOSING METATHESIS;

EID: 0037237184     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-37526     Document Type: Article

References (21)

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15. The iridium-catalyzed regioselective allylic amination was recently achieved by Takeuchi's group. See: (a) Takeuchi, R.; Ue, N.; Tanabe, K.; Yamashita, K.; Shiga, N. J. Am. Chem. Soc. 2001, 123, 9525. (b) Takeuchi, R.; Shiga, N. Org. Lett. 1999, 1, 265. (c) For a review, see: Takeuchi, R. Synlett 2002, 1954.
16. The iridium-catalyzed regioselective allylic amination was recently achieved by Takeuchi's group. See: (a) Takeuchi, R.; Ue, N.; Tanabe, K.; Yamashita, K.; Shiga, N. J. Am. Chem. Soc. 2001, 123, 9525. (b) Takeuchi, R.; Shiga, N. Org. Lett. 1999, 1, 265. (c) For a review, see: Takeuchi, R. Synlett 2002, 1954.
17. The iridium-catalyzed regioselective allylic amination was recently achieved by Takeuchi's group. See: (a) Takeuchi, R.; Ue, N.; Tanabe, K.; Yamashita, K.; Shiga, N. J. Am. Chem. Soc. 2001, 123, 9525. (b) Takeuchi, R.; Shiga, N. Org. Lett. 1999, 1, 265. (c) For a review, see: Takeuchi, R. Synlett 2002, 1954.
18. Recently, the effect of a hydroxylamine tether on intramolecular Diels-Alder reactions was reported. See: Ishikawa, T.; Senzaki, M.; Kadoya, R.; Morimoto, T.; Miyake, N.; Izawa, M.; Saito, S. J. Am. Chem. Soc. 2001, 123, 14607.
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21. 1H NMR, although these stereochemistries have not be determined.