New reaction protocols have been established to perform the reductive coupling of N-benzyl benzaldimines to 1,2-diphenyl-1,2-diaminoethanes in mild, stereoselective, and catalytic conditions by the use of SmI2 and Yb(OTf)(3). (C) 1998 Elsevier Science Ltd. All rights reserved.
Diastereoselective synthesis of 1,2-diphenyl-1,2-diaminoethanes by Yb(OTf)(3) accelerated reductive coupling of imines / R. Annunziata, M. Benaglia, M. Cinquini, F. Cozzi, L. Raimondi. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 39:20(1998), pp. 3333-3336. [10.1016/S0040-4039(98)00484-5]
Diastereoselective synthesis of 1,2-diphenyl-1,2-diaminoethanes by Yb(OTf)(3) accelerated reductive coupling of imines
R. AnnunziataPrimo
;M. BenagliaSecondo
;M. Cinquini;F. CozziPenultimo
;L. RaimondiUltimo
1998
Abstract
New reaction protocols have been established to perform the reductive coupling of N-benzyl benzaldimines to 1,2-diphenyl-1,2-diaminoethanes in mild, stereoselective, and catalytic conditions by the use of SmI2 and Yb(OTf)(3). (C) 1998 Elsevier Science Ltd. All rights reserved.
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