Lee, JG Choi, KI Pae, AN Koh, HY Kang, YH Cho, YS 2024-01-21T10:45:34Z 2024-01-21T10:45:34Z 2021-09-05 2002-04 1472-7781 https://pubs.kist.re.kr/handle/201004/139661 The hemiacetals of (+)- and (-)-N-glyoxyloylbornane-10,2-sultam and their imines reacted with allyl iodide in the presence of indium in DMF to give the corresponding alpha-hydroxy and alpha-amino camphor sultam derivatives with high diastereoselectivities (86-90% de). This method could be useful for preparation of alpha-hydroxy and alpha-amino acids. English ROYAL SOC CHEMISTRY Indium-mediated diastereoselective allylation reactions: preparation of alpha-hydroxy and alpha-amino acids Article 10.1039/b110505c 1 JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no.10, pp.1314 - 1317 JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 10 1314 1317 scie 000175509800016 Chemistry, Organic Chemistry Article diastereoselective