Literature DB >> 16855705

A modular approach to the synthesis of 2,3,4-trisubstituted tetrahydrofurans.

Christopher G Nasveschuk1, Nathan T Jui, Tomislav Rovis.   

Abstract

A highly diastereoselective Lewis acid-mediated [1,3] rearrangement of 1,3-dioxepins is the key step along a modular route to 2,3,4-trisubstituted tetrahydrofurans.

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Year:  2006        PMID： 16855705     DOI： 10.1039/b605438b

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


  3 in total

1.  Umpolung α-Silylation of Cyclopropyl Acetates via Low-Temperature Catalytic C-C Activation.

Authors:  Thirupataiah Avullala; Parham Asgari; Yuanda Hua; Apparao Bokka; Shawn G Ridlen; Kyungsuk Yum; H V Rasika Dias; Junha Jeon
Journal:  ACS Catal       Date:  2018-12-03       Impact factor: 13.084

2.  Catalytic Net Oxidative C-C Activation and Silylation of Cyclopropanols with a Traceless Acetal Directing Group.

Authors:  Thirupataiah Avullala; Hiep H Nguyen; Udaya Sree Dakarapu; Parham Asgari; Yuanda Hua; Junha Jeon
Journal:  ACS Catal       Date:  2022-01-18       Impact factor: 13.700

3.  Chiral Fe(ii) complex catalyzed enantioselective [1,3] O-to-C rearrangement of alkyl vinyl ethers and synthesis of chromanols and beyond.

Authors:  Lifeng Wang; Pengfei Zhou; Qianchi Lin; Shunxi Dong; Xiaohua Liu; Xiaoming Feng
Journal:  Chem Sci       Date:  2020-09-07       Impact factor: 9.825
  3 in total

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