Improvement of Diastereoselectivity in Oxyselenenylation of Cyclohexene with (R,R)-Hydrobenzoin Employing Chiral Selenium and Achiral Methylselenium Electrophiles

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J. Chem. Soc. Chem. Commun. v.1945 Kim, K. S.;park, J. I.;Moon, H. K.;Yi, H.
Angew. Chem. Int. Ed. v.39 For a recent review of Organoselenium chemistry in stereoselectove reactions, see:Wirth, T.
Tetrahedron v.55 For a recent review of chiral selenium compounds, see:Wirth, T.
Reviews on Heteroatom Chemistry v.16 For a review of asymmetric oxyselenenylation, see:Fujita, K.
J. Am. Chem. Soc. v.121 For a theoretical study on the origin of stereoselectivity in asymmetric oxyselenenylation, see Wang, X.;Houk, K. N.;Spichty, M.;Wirth, T.
Chem. Lett. v.1123 For an example of oxyselenenylation with chiral nucleophiles, see:Fujita, K.;Iwaoka, M.;Tomoda, S.
J. Org. Chem. v.59 Rosini, C.;Scamuzzi, S.;Uccello-Barretta, G.;Salvadori, P.
Chem. Ber. v.110 Paulsen, H.;Brauer, O.

ChemInform Abstract: Improvement of Diastereoselectivity in Oxyselenenylation of Cyclohexene with (R,R)-Hydrobenzoin Employing Chiral Selenium and Achiral Methylselenium Electrophiles. vol.33, pp.15, 2001, https://doi.org/10.1002/chin.200215030