Literature DB >> 15274210

Nickel-catalyzed reductive cyclizations and couplings.

John Montgomery1.   

Abstract

For over 50 years, nickel catalysis has been applied in cycloaddition processes. Nickel-catalyzed reductive couplings and cyclizations, however, have only recently attracted a high level of interest. This group of new reactions allows a broad range of multicomponent couplings involving two or more pi components with a main-group or transition-metal reagent. These processes allow the assembly of important organic substructures from widely available reaction components. Multiple contiguous stereocenters, polycyclic ring systems, and novel arrays of complex functionality may often be prepared from simple, achiral, acyclic precursors. With three or more reactive functional groups participating in the catalytic processes, many mechanistic questions abound, including the precise timing of bond constructions and the nature of reactive intermediates. This Review is thus aimed at providing a critical evaluation of recent progress in this rapidly developing field.

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Year:  2004        PMID: 15274210     DOI: 10.1002/anie.200300634

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  84 in total

1.  Nickel-Catalyzed Reductive [2+2] Cycloaddition of Alkynes.

Authors:  Santiago Cañellas; John Montgomery; Miquel À Pericàs
Journal:  J Am Chem Soc       Date:  2018-12-10       Impact factor: 15.419

2.  Diastereoselective Nickel-Catalyzed Reductive Couplings of Aminoaldehydes and Alkynylsilanes: Application to the Synthesis of D-erythro-Sphingosine.

Authors:  Kanicha Sa-Ei; John Montgomery
Journal:  Tetrahedron       Date:  2009-09-15       Impact factor: 2.457

3.  New N-heterocyclic carbene ligand and its application in asymmetric nickel-catalyzed aldehyde/alkyne reductive couplings.

Authors:  Mani Raj Chaulagain; Grant J Sormunen; John Montgomery
Journal:  J Am Chem Soc       Date:  2007-07-12       Impact factor: 15.419

4.  Alpha-olefins as alkenylmetal equivalents in catalytic conjugate addition reactions.

Authors:  Chun-Yu Ho; Hirohisa Ohmiya; Timothy F Jamison
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

Review 5.  Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents.

Authors:  John F Bower; In Su Kim; Ryan L Patman; Michael J Krische
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

6.  Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: a ruthenium-catalyzed C-C bond-forming transfer hydrogenation.

Authors:  Ryan L Patman; Vanessa M Williams; John F Bower; Michael J Krische
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

7.  Nickel Catalysis: Synergy between Method Development and Total Synthesis.

Authors:  Eric A Standley; Sarah Z Tasker; Kim L Jensen; Timothy F Jamison
Journal:  Acc Chem Res       Date:  2015-04-23       Impact factor: 22.384

8.  Total synthesis of (+)-acutiphycin.

Authors:  Ryan M Moslin; Timothy F Jamison
Journal:  J Org Chem       Date:  2007-11-07       Impact factor: 4.354

9.  Diastereoselective construction of functionalized homoallylic alcohols by Ni-catalyzed diboron-promoted coupling of dienes and aldehydes.

Authors:  Hee Yeon Cho; James P Morken
Journal:  J Am Chem Soc       Date:  2008-12-03       Impact factor: 15.419

10.  Allene-alkyne cross-coupling for stereoselective synthesis of substituted 1,4-dienes and cross-conjugated trienes.

Authors:  Heidi L Shimp; Alissa Hare; Martin McLaughlin; Glenn C Micalizio
Journal:  Tetrahedron       Date:  2008-04-14       Impact factor: 2.457

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