Literature DB >> 19760721

Synthesis and reactivity of enantiomerically enriched thiiranium ions.

Scott E Denmark1, Thomas Vogler.   

Abstract

Enantiomerically enriched thiiranium ion 5 has been prepared by silver-assisted ionization of chloro sulfide 4 at -20 degrees C. This thiiranium ion is configurationally stable in solution up to room temperature as demonstrated by the stereospecific capture of the ion by various oxygen- and nitrogen-based nucleophiles. Both isolated olefins and weak Lewis bases can promote the racemization of 5 but these processes can also be suppressed at low temperature. Capture of 5 by methanol is faster than the racemization processes.

Entities:  

Year:  2009        PMID: 19760721     DOI: 10.1002/chem.200901377

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  26 in total

1.  Structural, Mechanistic, Spectroscopic, and Preparative Studies on the Lewis Base Catalyzed, Enantioselective Sulfenofunctionalization of Alkenes.

Authors:  Eduard Hartmann; Scott E Denmark
Journal:  Helv Chim Acta       Date:  2017-09-14       Impact factor: 2.164

Review 2.  Catalytic, Enantioselective Sulfenofunctionalization of Alkenes: Development and Recent Advances.

Authors:  Anastassia Matviitsuk; Jesse L Panger; Scott E Denmark
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-18       Impact factor: 15.336

3.  Retention or inversion in stereospecific nickel-catalyzed cross-coupling of benzylic carbamates with arylboronic esters: control of absolute stereochemistry with an achiral catalyst.

Authors:  Michael R Harris; Luke E Hanna; Margaret A Greene; Curtis E Moore; Elizabeth R Jarvo
Journal:  J Am Chem Soc       Date:  2013-02-22       Impact factor: 15.419

4.  Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.

Authors:  Elizabeth C Swift; Elizabeth R Jarvo
Journal:  Tetrahedron       Date:  2013-07-22       Impact factor: 2.457

5.  Catalytic asymmetric thiofunctionalization of unactivated alkenes.

Authors:  Scott E Denmark; David J P Kornfilt; Thomas Vogler
Journal:  J Am Chem Soc       Date:  2011-09-14       Impact factor: 15.419

6.  Catalytic, enantioselective, intramolecular carbosulfenylation of olefins. Preparative and stereochemical aspects.

Authors:  Scott E Denmark; Alex Jaunet
Journal:  J Org Chem       Date:  2013-12-11       Impact factor: 4.354

7.  Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives.

Authors:  Sarah M Pound; Mary P Watson
Journal:  Chem Commun (Camb)       Date:  2018-10-30       Impact factor: 6.222

8.  Catalytic, enantioselective, intramolecular carbosulfenylation of olefins.

Authors:  Scott E Denmark; Alex Jaunet
Journal:  J Am Chem Soc       Date:  2013-04-19       Impact factor: 15.419

9.  Combining NHC-Cu and Brønsted base catalysis: enantioselective allylic substitution/conjugate additions with alkynylaluminum reagents and stereospecific isomerization of the products to trisubstituted allenes.

Authors:  Jennifer A Dabrowski; Fredrik Haeffner; Amir H Hoveyda
Journal:  Angew Chem Int Ed Engl       Date:  2013-06-18       Impact factor: 15.336

10.  Lewis Base Activation of Lewis Acids - Group 13. In Situ Generation and Reaction of Borenium Ions.

Authors:  Scott E Denmark; Yusuke Ueki
Journal:  Organometallics       Date:  2013-11-25       Impact factor: 3.876

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