Catalytic asymmetric synthesis using P-chiral diaminophosphine oxide preligands: DIAPHOXs

Tetrahedron

Volumn 67, Issue 4, 2011, Pages 667-687

  Nemoto, Tetsuhiro ^a   Hamada, Yasumasa ^a  

^a CHIBA UNIVERSITY   (Japan)

Author keywords

Asymmetric allylic substitution; Asymmetric catalysis; Diaminophosphine oxide; Iridium; Palladium; Secondary phosphine oxide

Indexed keywords

ALLENE DERIVATIVE; AROMATIC AMINE; CARBON; CARBONIC ACID DERIVATIVE; DIAMINOPHOSPHINE OXIDE; NITROGEN; NITROMETHANE; NUCLEOPHILE; PALLADIUM; PHOSPHINE OXIDE DERIVATIVE; TANGUTORINE; UNCLASSIFIED DRUG;

ALKYLATION; AMINATION; ARTICLE; ASYMMETRIC SYNTHESIS; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOMER; ENANTIOSELECTIVITY; MORITA BAYLIS HILLMAN REACTION; PRIORITY JOURNAL; SUBSTITUTION REACTION; SYNTHESIS;

EID: 78650559751     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.11.069     Document Type: Review

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198. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: T. Kanayama, K. Yoshida, H. Miyabe, T. Kimachi, and Y. Takemoto J. Org. Chem. 68 2003 6197
199. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: N. Kinoshita, K.H. Marx, K. Tanaka, K. Tsubaki, T. Kawabata, N. Yoshikai, E. Nakamura, and K. Fuji J. Org. Chem. 69 2004 7960
200. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: A. Alexakis, and D. Polet Org. Lett. 6 2004 3529
201. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: G. Lipowsky, N. Miller, and G. Helmchen Angew. Chem., Int. Ed. 43 2004 4595
202. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: S. Streiff, C. Welter, M. Schelwiss, G. Lipowsky, N. Miller, and G. Helmchen Chem. Commun. 2005 2957
203. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: T. Graening, and J.F. Hartwig J. Am. Chem. Soc. 127 2005 17192
204. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: D. Polet, A. Alexakis, K. Tissot-Croset, C. Corminboeuf, and K. Ditrich Chem. - Eur. J. 12 2006 3596
205. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: G. Onodera, K. Watabe, M. Matsubara, K. Oda, S. Kezuka, and R. Takeuchi Adv. Synth. Catal. 350 2008 2725
206. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: L.M. Stanley, C. Bai, M. Ueda, and J.F. Hartwig J. Am. Chem. Soc. 132 2010 8918
207. For a representative example of Ir-catalyzed asymmetric allylic alkylation, see: F. Giacomina, D. Riat, and A. Alexakis Org. Lett. 12 2010 1156
208. For a representative example of Ir-catalyzed asymmetric allylic etherification, see: C. Shu, and J.F. Hartwig Angew. Chem., Int. Ed. 43 2004 4794
209. For a representative example of Ir-catalyzed asymmetric allylic etherification, see: I. Lyothier, C. Defieber, and E.M. Carreira Angew. Chem., Int. Ed. 45 2006 6204
210. For a representative example of Ir-catalyzed asymmetric allylic etherification, see: M. Kimura, and Y. Uozumi J. Org. Chem. 72 2007 707
211. For a representative example of Ir-catalyzed asymmetric allylic etherification, see: S. Ueno, and J.F. Hartwig Angew. Chem., Int. Ed. 47 2008 1928
212. For a catalytic asymmetric synthesis of paroxetine, see: T. Senda, M. Ogasawara, and T. Hayashi J. Org. Chem. 66 2001 6852
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