698394-45-5Relevant academic research and scientific papers
Iodine-mediated ring-closing iodoamination with concomitant N-debenzylation for the asymmetric synthesis of polyhydroxylated pyrrolidines
Davies, Stephen G.,Nicholson, Rebecca L.,Price, Paul D.,Roberts, Paul M.,Russell, Angela J.,Savory, Edward D.,Smith, Andrew D.,Thomson, James E.
experimental part, p. 758 - 772 (2009/09/30)
Treatment of a range of homochiral unsaturated β-amino esters (containing a cis-dioxolane unit) with iodine promotes a novel ring-closing alkene iodoamination reaction which proceeds with concomitant N-debenzylation, providing a simple and stereoselective
Iodine-mediated ring closing alkene iodoamination with N-debenzylation for the asymmetric synthesis of polyhydroxylated pyrrolidines
Davies, Stephen G.,Nicholson, Rebecca L.,Price, Paul D.,Roberts, Paul M.,Smith, Andrew D.
, p. 901 - 903 (2007/10/03)
An iodine-mediated ring closing alkene iodoamination with N-debenzylation protocol provides a direct route for the asymmetric synthesis of polyhydroxylated pyrrolidines from homochiral β-amino acid derivatives.
