Literature DB >> 11667380

Scandium Trifluoromethanesulfonate as an Extremely Active Lewis Acid Catalyst in Acylation of Alcohols with Acid Anhydrides and Mixed Anhydrides.

Kazuaki Ishihara1, Manabu Kubota, Hideki Kurihara, Hisashi Yamamoto.   

Abstract

Scandium trifluoromethanesulfonate (triflate), which is commercially available, is a practical and useful Lewis acid catalyst for acylation of alcohols with acid anhydrides or the esterification of alcohols by carboxylic acids in the presence of p-nitrobenzoic anhydrides. The remarkably high catalytic activity of scandium triflate can be used for assisting the acylation by acid anhydrides of not only primary alcohols but also sterically-hindered secondary or tertiary alcohols. The method presented is especially effective for selective macrolactonization of omega-hydroxy carboxylic acids.

Entities:  

Year:  1996        PMID: 11667380     DOI: 10.1021/jo952237x

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  12 in total

1.  Asymmetric multi-component reactions: convenient access to acyclic stereocenters and functionalized cyclopentenoids.

Authors:  Arun K Ghosh; Sarang S Kulkarni; Chun-Xiao Xu; Khriesto Shurrush
Journal:  Tetrahedron Asymmetry       Date:  2008-05-01

2.  Convergent route to the spirohexenolide macrocycle.

Authors:  Brian D Jones; James J La Clair; Curtis E Moore; Arnold L Rheingold; Michael D Burkart
Journal:  Org Lett       Date:  2010-10-15       Impact factor: 6.005

3.  Indium triflate catalyzed peracetylation of carbohydrates.

Authors:  Nicholas P Bizier; Shannon R Atkins; Luke C Helland; Shane F Colvin; Joseph R Twitchell; Mary J Cloninger
Journal:  Carbohydr Res       Date:  2008-04-10       Impact factor: 2.104

4.  Rh(I)-catalyzed cyclocarbonylation of allenol esters to prepare acetoxy 4-alkylidenecyclopent-3-en-2-ones.

Authors:  Kay M Brummond; Matthew M Davis; Chaofeng Huang
Journal:  J Org Chem       Date:  2009-11-06       Impact factor: 4.354

5.  Novobiocin Enhances Polymyxin Activity by Stimulating Lipopolysaccharide Transport.

Authors:  Michael D Mandler; Vadim Baidin; James Lee; Karanbir S Pahil; Tristan W Owens; Daniel Kahne
Journal:  J Am Chem Soc       Date:  2018-05-16       Impact factor: 15.419

6.  One-pot odourless synthesis of thioesters via in situ generation of thiobenzoic acids using benzoic anhydrides and thiourea.

Authors:  Mohammad Abbasi; Reza Khalifeh
Journal:  Beilstein J Org Chem       Date:  2015-07-28       Impact factor: 2.883

7.  ZSM-5-SO3H: An Efficient Catalyst for Acylation of Sulfonamides Amines, Alcohols, and Phenols under Solvent-Free Conditions.

Authors:  Ahmad Reza Massah; Roozbeh Javad Kalbasi; Mahdiehsadat Khalifesoltani; Fariba Moshtagh Kordesofla
Journal:  ISRN Org Chem       Date:  2013-12-08

8.  Resolution of Racemic α-Hydroxyphosphonates: Bi(OTf)3-Catalyzed Stereoselective Esterification of α-Hydroxyphosphonates with (+)-Dibenzoyl-l-tartaric Anhydride.

Authors:  Babak Kaboudin; Sajedeh Alavi; Foad Kazemi; Hiroshi Aoyama; Tsutomu Yokomatsu
Journal:  ACS Omega       Date:  2019-09-10

9.  Umpolung amide synthesis using substoichiometric N-iodosuccinimide (NIS) and oxygen as a terminal oxidant.

Authors:  Kenneth E Schwieter; Bo Shen; Jessica P Shackleford; Matthew W Leighty; Jeffrey N Johnston
Journal:  Org Lett       Date:  2014-09-08       Impact factor: 6.005

10.  Ruthenium(III) chloride catalyzed acylation of alcohols, phenols, and thiols in room temperature ionic liquids.

Authors:  Zhiwen Xi; Wenyan Hao; Pingping Wang; Mingzhong Cai
Journal:  Molecules       Date:  2009-09-10       Impact factor: 4.411

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