A convenient approach to racemic analogues of N-benzoyl-syn-phenylisoserine was realized via the stereoselective iodocyclization of amides obtained from Baylis-Hillman adducts.
Stereoselective iodocyclisation of 3-acylamino-3-aryl-2-methylenealkanoates: synthesis of analogs of N-benzoyl-syn-phenylisoserine / Galeazzi, Roberta; Mobbili, Giovanna; Mobbili, G; Orena, Mario; Rinaldi, Samuele. - In: ORGANIC LETTERS. - ISSN 1523-7060. - 6:(2004), pp. 2571-2574.
Stereoselective iodocyclisation of 3-acylamino-3-aryl-2-methylenealkanoates: synthesis of analogs of N-benzoyl-syn-phenylisoserine
GALEAZZI, ROBERTA;MOBBILI, Giovanna;ORENA, MARIO;RINALDI, SAMUELE
2004-01-01
Abstract
A convenient approach to racemic analogues of N-benzoyl-syn-phenylisoserine was realized via the stereoselective iodocyclization of amides obtained from Baylis-Hillman adducts.File in questo prodotto:
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