Literature DB >> 20222089

Anatomy of long-lasting love affairs with lithium carbenoids: past and present status and future prospects.

Vito Capriati1, Saverio Florio.   

Abstract

After a long adolescence, the chemistry of lithium carbenoids has currently been entering its maturity bringing a dowry of a more in-depth and less empirical knowledge of the structure and configurational stability of such double-faced intermediates; this, thanks in particular to the synergistic and harmonic cooperation between calculations and the most modern NMR techniques now at our disposal. Such knowledge has stimulated the development of fruitful stereoselective applications in the field of organic synthesis, providing in addition a rationale to observed selectivities. Such aspects together with the role played by aggregation and solvation on the structure-reactivity relationship are highlighted throughout this Minireview with selected examples extracted from recent literature.

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Year:  2010        PMID: 20222089     DOI: 10.1002/chem.200902870

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


  12 in total

1.  New insights into the insertion reactions of germylenoid H2GeLiF with RH (R = F, OH, NH2).

Authors:  Bingfei Yan; Wenzuo Li; Cuiping Xiao; Zhenbo Liu; Qingzhong Li; Jianbo Cheng
Journal:  J Mol Model       Date:  2015-03-07       Impact factor: 1.810

2.  Insight into the substitution reactions of silylenoid H2SiLiF with GeH3X (X = F, Cl, Br): a theoretical study.

Authors:  Bingfei Yan; Wenzuo Li; Cuiping Xiao; Qingzhong Li; Jianbo Cheng
Journal:  J Mol Model       Date:  2015-03-10       Impact factor: 1.810

3.  Consecutive and Selective Double Methylene Insertion of Lithium Carbenoids to Isothiocyanates: A Direct Assembly of Four-Membered Sulfur-Containing Cycles.

Authors:  Raffaele Senatore; Monika Malik; Thierry Langer; Wolfgang Holzer; Vittorio Pace
Journal:  Angew Chem Int Ed Engl       Date:  2021-10-13       Impact factor: 16.823

4.  A new reaction mode of germanium-silicon bond formation: insertion reactions of H₂GeLiF with SiH₃X (X = F, Cl, Br).

Authors:  Bingfei Yan; Wenzuo Li; Cuiping Xiao; Qingzhong Li; Jianbo Cheng
Journal:  J Mol Model       Date:  2013-08-16       Impact factor: 1.810

5.  On the Configurational Stability of Chiral Heteroatom-Substituted [D1]Methylpalladium Complexes as Intermediates of Stille and Suzuki-Miyaura Cross-Coupling Reactions.

Authors:  Petra Malova Krizkova; Friedrich Hammerschmidt
Journal:  European J Org Chem       Date:  2013-06-27

6.  Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α-Oxy- and α-Thio-Substituted Organolithium Species.

Authors:  Alexander P Pulis; Ana Varela; Cinzia Citti; Pradip Songara; Daniele Leonori; Varinder K Aggarwal
Journal:  Angew Chem Int Ed Engl       Date:  2017-08-07       Impact factor: 15.336

7.  Water opens the door to organolithiums and Grignard reagents: exploring and comparing the reactivity of highly polar organometallic compounds in unconventional reaction media towards the synthesis of tetrahydrofurans.

Authors:  Luciana Cicco; Stefania Sblendorio; Rosmara Mansueto; Filippo M Perna; Antonio Salomone; Saverio Florio; Vito Capriati
Journal:  Chem Sci       Date:  2015-11-03       Impact factor: 9.825

8.  A practical guide for using lithium halocarbenoids in homologation reactions.

Authors:  Serena Monticelli; Marta Rui; Laura Castoldi; Giada Missere; Vittorio Pace
Journal:  Monatsh Chem       Date:  2018-06-11       Impact factor: 1.451

9.  Telescoped, Divergent, Chemoselective C1 and C1-C1 Homologation of Imine Surrogates: Access to Quaternary Chloro- and Halomethyl-Trifluoromethyl Aziridines.

Authors:  Laura Ielo; Saad Touqeer; Alexander Roller; Thierry Langer; Wolfgang Holzer; Vittorio Pace
Journal:  Angew Chem Int Ed Engl       Date:  2019-01-24       Impact factor: 15.336

10.  On the preparation and determination of configurational stability of chiral thio- and bromo[D1]methyllithiums.

Authors:  Anna Wieczorek; Friedrich Hammerschmidt
Journal:  J Org Chem       Date:  2012-10-30       Impact factor: 4.354

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