Kim, Hyoungsu Seo, Jae Hong Shin, Kye Jung Kim, Dong Jin Kim, Deukjoon 2024-01-21T01:36:18Z 2024-01-21T01:36:18Z 2022-01-10 2006-12-31 0385-5414 https://pubs.kist.re.kr/handle/201004/134803 An efficient, novel synthetic strategy has been developed for preparation of cyclic alpha-amino acid employing an intermolecular hetero Diels-Alder reaction and an intramolecular hydantoin enolate alkylation as key steps. Application of the present hetero Diels-Alder/intramolecular hydantoin alkylation methodology to synthesis of halichlorine was explored. English PERGAMON-ELSEVIER SCIENCE LTD VCAM-1 INDUCTION DERIVATIVES INHIBITOR An approach to cyclic alpha-amino acids by a novel hetero Diels-Alder/intramolecular hydantoin enolate alkylation strategy: An approach to halichlorine Article 1 HETEROCYCLES, v.70, pp.143 - + HETEROCYCLES 70 143 + scie scopus 000244442800018 2-s2.0-33947674836 Chemistry, Organic Chemistry Article VCAM-1 INDUCTION DERIVATIVES INHIBITOR cyclic alpha-amino acid hetero diels-alder reaction intramolecular hydantoin enolate alkylation C- vs O-alkylation halichlorine