Son Eun Chae, Kim Seung Yeon, Kim Sung-Gon
Department of Chemistry, College of Natural Science, Kyonggi University, 154-42 Gwanggyosan-ro, Yeongtong-gu, Suwon 16227, Republic of Korea.
J Org Chem. 2021 May 7;86(9):6826-6839. doi: 10.1021/acs.joc.1c00715. Epub 2021 Apr 27.
Organocatalytic enantioselective intramolecular oxa-Michael reactions of benzyl alcohol bearing α,β-unsaturated carbonyls as Michael acceptors are presented herein. Using cinchona squaramide-based organocatalyst, enones as well as α,β-unsaturated esters containing benzyl alcohol provided their corresponding 1,3-dihydroisobenzofuranyl-1-methylene ketones and 1,3-dihydroisobenzofuranyl-1-methylene esters in excellent yields with high enantioselectivities. In addition, enantioenriched 1,3-dihydroisobenzofuranyl-1-methylene ketone could be obtained from the Wittig/oxa-Michael reaction cascade of 1,3-dihydro-2-benzofuran-1-ol.
本文介绍了以含α,β-不饱和羰基的苯甲醇作为迈克尔受体的有机催化对映选择性分子内氧杂-迈克尔反应。使用基于金鸡纳方酰胺的有机催化剂,烯酮以及含苯甲醇的α,β-不饱和酯以优异的产率和高对映选择性得到了相应的1,3-二氢异苯并呋喃-1-亚甲基酮和1,3-二氢异苯并呋喃-1-亚甲基酯。此外,对映体富集的1,3-二氢异苯并呋喃-1-亚甲基酮可通过1,3-二氢-2-苯并呋喃-1-醇的维蒂希/氧杂-迈克尔反应串联得到。