Chemo- and regioselective reductive opening of azetidinium ions

Tetrahedron Letters

Volumn 48, Issue 6, 2007, Pages 1027-1031

  Couty, François ^a   David, Olivier ^a   Durrat, François ^a  

^a UNIVERSITÉ DE VERSAILLES SAINT QUENTIN EN YVELINES   (France)

Author keywords

Azetidines; Azetidinium ions; Reduction; Strain

Indexed keywords

ALUMINUM DERIVATIVE; AMINOALCOHOL; AZETIDINE DERIVATIVE; DIAMINE; ESTER DERIVATIVE; LITHIUM DERIVATIVE; NITRILE; REAGENT; SODIUM BOROHYDRIDE; TRIFLUOROMETHANESULFONIC ACID;

ARTICLE; CHEMICAL REACTION; ENANTIOMER;

EID: 33846036970     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.11.175     Document Type: Article

References (20)

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13. 6a,6c (opening with phosphorous-stabilized C-nucleophiles). See also:. Wills M.T., Wills I.E., Von Dollen L., Butler B.L., Porter J., and Anderson A.G. J. Org. Chem. 45 (1980) 2489-2498 (opening with BuLi)
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16. For the preparation of these substrates, see: Ref. 3 and references cited therein.
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