Diastereo‐ and Enantioselective Synthesis of Bisbenzannulated Spiroketals and Spiroaminals by Ir/Ag/Acid Ternary Catalysis

• Published in: Angewandte Chemie International Edition Vol. 61; no. 42; pp. e202210207 - n/a
• Main Authors: Yang, Wu‐Lin, Shang, Xin‐Yu, Ni, Tao, Yan, Hui, Luo, Xiaoyan, Zheng, Hanliang, Li, Zhong, Deng, Wei‐Ping
• Format: Journal Article
• Language: English
• Published: WEINHEIM Wiley 17.10.2022; Wiley Subscription Services, Inc
• Edition: International ed. in English
• Subjects: Allyl compounds; Allylation; Aniline; Asymmetric Synthesis; Cascade chemical reactions; Catalysis; catalytic activity; Chemical reactions; Chemistry; Chemistry, Multidisciplinary; Enantiomers; enantioselective synthesis; Iridium; Isomerization; Phenols; Physical Sciences; Reaction mechanisms; Science & Technology; Silver; Spiroketals; Stereochemistry; Stereoselectivity; Ternary Catalysis; ASYMMETRIC-SYNTHESIS; ACID; HYDROGENATION; ALLYLIC ALKYLATION; ALKYNYLBENZALDEHYDES; Allylation; Ternary Catalysis; CYCLOADDITION; BETA-ALKYNYL KETONES; LIGANDS; BIOLOGICAL-ACTIVITY; Spiroketals; Asymmetric Synthesis; Iridium; DERIVATIVES

We reported herein an iridium/silver/acid ternary catalytic system to access bisbenzannulated [6,6]‐spiroketals in high efficiency with generally high diastereo‐ and enantioselectivities (up to >20 : 1 dr, >99 % ee). In this procedure, readily available o‐alkynylacetophenones undergo cycloisom...