Literature DB >> 21491870

Phosphine-catalyzed β'-umpolung addition of nucleophiles to activated α-alkyl allenes.

Tioga J Martin1, Venus G Vakhshori, Yang S Tran, Ohyun Kwon.   

Abstract

Highly functionalized alkenes can be prepared through phosphine-catalyzed β'-umpolung additions of nucleophiles (carbon-, oxygen-, nitrogen-, and sulfur-centered) to activated α-disubstituted allenes, providing many potentially useful synthetic intermediates in good to excellent yields, often with high levels of stereoselectivity for the product olefin geometry. Various substitution patterns around the allene are compatible with the process, showcasing the synthetic utility of allenes under the conditions of nucleophilic phosphine catalysis.

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Year:  2011        PMID: 21491870      PMCID: PMC3094471          DOI: 10.1021/ol200697m

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  28 in total

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  8 in total

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2.  Stereoselective Syntheses of α,β-Unsaturated γ-Amino Esters Through Phosphine-Catalyzed γ-Umpolung Additions of Sulfonamides to γ-Substituted Allenoates.

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Review 3.  Phosphine Organocatalysis.

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4.  Phosphine-catalyzed intramolecular γ-umpolung addition of α-aminoalkylallenic esters: facile synthesis of 3-carbethoxy-2-alkyl-3-pyrrolines.

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5.  Advances in nucleophilic phosphine catalysis of alkenes, allenes, alkynes, and MBHADs.

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Journal:  Chem Commun (Camb)       Date:  2013-12-25       Impact factor: 6.222

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8.  Reaction of allene esters with Selectfluor/TMSX (X = I, Br, Cl) and Selectfluor/NH4SCN: Competing oxidative/electrophilic dihalogenation and nucleophilic/conjugate addition.

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  8 in total

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