Literature DB >> 22618414

Exploiting a novel size exclusion phenomenon for enantioselective acid/base cascade catalysis.

Michael E Muratore1, Lei Shi, Adam W Pilling, R Ian Storer, Darren J Dixon.   

Abstract

A novel size exclusion phenomenon between PS-BEMP and sterically bulky BPAs, has been discovered and exploited in a one-pot base-catalysed Michael addition/acid-catalysed enantioselective N-acyliminium cyclisation cascade, allowing the preparation of structurally complex β-carbolines with moderate to good enantiocontrol.

Entities:  

Year:  2012        PMID: 22618414     DOI: 10.1039/c2cc32258g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Nickel-Catalyzed Amidoalkylation Reaction of γ-Hydroxy Lactams: An Access to 3-Substituted Isoindolinones.

Authors:  Shuo Zhang; Xinhua Shi; Jichao Li; Zitong Hou; Zihe Song; Xiaofeng Su; Dan Peng; Feng Wang; Yitao Yu; Guilong Zhao
Journal:  ACS Omega       Date:  2019-11-05

Review 2.  The Pictet-Spengler Reaction Updates Its Habits.

Authors:  Andrea Calcaterra; Laura Mangiardi; Giuliano Delle Monache; Deborah Quaglio; Silvia Balducci; Simone Berardozzi; Antonia Iazzetti; Roberta Franzini; Bruno Botta; Francesca Ghirga
Journal:  Molecules       Date:  2020-01-19       Impact factor: 4.411

  2 in total

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