Literature DB >> 12762776

New, improved procedure for the synthesis of structurally diverse N-spiro C2-symmetric chiral quaternary ammonium bromides.

Takashi Ooi1, Yukitaka Uematsu, Keiji Maruoka.   

Abstract

Selective, direct ortho magnesiation of (S)-2,2'-bis(isopropoxycarbonyl)-1,1'-binaphthyl (6) has been achieved under mild conditions, using magnesium bis(2,2,6,6-tetramethylpiperamide) [Mg(TMP)(2)]. In combination with the subsequent reaction with the appropriate electrophiles, bromine and iodine, this method constitutes a key step in establishing a new and concise synthetic route to a wide variety of N-spiro C(2)-symmetric chiral quaternary ammonium bromides of type 1.

Entities:  

Year:  2003        PMID: 12762776     DOI: 10.1021/jo030032f

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


  3 in total

1.  Alkylative kinetic resolution of vicinal diols under phase-transfer conditions: a chiral ammonium borinate catalysis.

Authors:  Martin Pawliczek; Takuya Hashimoto; Keiji Maruoka
Journal:  Chem Sci       Date:  2017-12-12       Impact factor: 9.825

2.  Improved Access to Chiral Tetranaphthoazepinium-Based Organocatalysts Using Aqueous Ammonia as Nitrogen Source.

Authors:  Auraya Manaprasertsak; Sorachat Tharamak; Christina Schedl; Alexander Roller; Michael Widhalm
Journal:  Molecules       Date:  2019-10-25       Impact factor: 4.411

3.  Economy of Catalyst Synthesis-Convenient Access to Libraries of Di- and Tetranaphtho Azepinium Compounds.

Authors:  Sorachat Tharamak; Christian Knittl-Frank; Auraya Manaprasertsak; Anchulee Pengsook; Lydia Suchy; Philipp Schuller; Barbara Happl; Alexander Roller; Michael Widhalm
Journal:  Molecules       Date:  2018-03-24       Impact factor: 4.411

  3 in total

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