{"title":"α-亚胺酮的芳基化及其与烯丙酸酯的环化:直接接触位阻吡咯","authors":"Srinivasarao Yaragorla , Doma Arun","doi":"10.1002/ajoc.202400756","DOIUrl":null,"url":null,"abstract":"<div><div>Herein, we report a calcium‐catalyzed, one‐pot, four‐component reaction to synthesize diversely substituted pyrroles. This atom‐economy reaction involves a sequence of reactions that proceed via in situ formation of α ‐ imino ketones, Friedel‐Crafts arylation, aza‐cyclization, and aromatization in the single pot. The reaction showed a broad substrate scope with good yields. We demonstrated the gram‐scale synthesis and post‐synthetic modifications.</div></div>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"14 4","pages":"Article e202400756"},"PeriodicalIF":2.8000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Arylation of α‐Imino Ketones and their Cyclization with Allenoates: Direct Access to Sterically Hindered Pyrroles\",\"authors\":\"Srinivasarao Yaragorla , Doma Arun\",\"doi\":\"10.1002/ajoc.202400756\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Herein, we report a calcium‐catalyzed, one‐pot, four‐component reaction to synthesize diversely substituted pyrroles. This atom‐economy reaction involves a sequence of reactions that proceed via in situ formation of α ‐ imino ketones, Friedel‐Crafts arylation, aza‐cyclization, and aromatization in the single pot. The reaction showed a broad substrate scope with good yields. We demonstrated the gram‐scale synthesis and post‐synthetic modifications.</div></div>\",\"PeriodicalId\":130,\"journal\":{\"name\":\"Asian Journal of Organic Chemistry\",\"volume\":\"14 4\",\"pages\":\"Article e202400756\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2193580725000479\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2193580725000479","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Arylation of α‐Imino Ketones and their Cyclization with Allenoates: Direct Access to Sterically Hindered Pyrroles
Herein, we report a calcium‐catalyzed, one‐pot, four‐component reaction to synthesize diversely substituted pyrroles. This atom‐economy reaction involves a sequence of reactions that proceed via in situ formation of α ‐ imino ketones, Friedel‐Crafts arylation, aza‐cyclization, and aromatization in the single pot. The reaction showed a broad substrate scope with good yields. We demonstrated the gram‐scale synthesis and post‐synthetic modifications.
期刊介绍:
Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC)
The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.