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Volumn 52, Issue 8, 2013, Pages 2260-2264

Palladium-catalyzed asymmetric allylic alkylation of 3-aryloxindoles with allylidene dipivalate: A useful enol pivalate product

Author keywords

allylic alkylation; asymmetric catalysis; heterocycles; Michael addition; palladium

Indexed keywords

ALLYLIC ALKYLATION; ASYMMETRIC ALLYLIC ALKYLATIONS; ASYMMETRIC CATALYSIS; HETEROCYCLES; HIGH YIELD; MICHAEL ADDITIONS; PALLADIUM-CATALYZED;

EID: 84873929178     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201209783     Document Type: Article
Times cited : (45)

References (57)
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    • 3 is used as the ligand; however, the use of ligand L1 with this system favors branched material. See also.
    • 3 is used as the ligand; however, the use of ligand L1 with this system favors branched material. See also, B. M. Trost, J. Vercauteren, Tetrahedron Lett. 1985, 26, 131.
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    • Trost, B.M.1    Vercauteren, J.2
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    • references therein. For the asymmetric allylic alkylation and benzylation of oxindole nucleophiles using Mo- and Pd-AAA, see
    • J. E. M. N. Klein, R. J. K. Taylor, Eur. J. Org. Chem. 2011, 6821, and references therein. For the asymmetric allylic alkylation and benzylation of oxindole nucleophiles using Mo- and Pd-AAA, see
    • (2011) Eur. J. Org. Chem. , pp. 6821
    • Klein, J.E.M.N.1    Taylor, R.J.K.2
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    • 84872539386 scopus 로고    scopus 로고
    • (Eds.: J. L. Vicario, D. Badia, L. Carrillo, E. Reyes), RSC Catalysis Series No. 5, RSC Publishing, Oxford.
    • Organocatalytic Enantioselective Conjugate Addition Reactions (Eds.:, J. L. Vicario, D. Badia, L. Carrillo, E. Reyes,), RSC Catalysis Series No. 5, RSC Publishing, Oxford, 2010.
    • (2010) Organocatalytic Enantioselective Conjugate Addition Reactions
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    • Following our submission of this manuscript, a report from Lu and co-workers on chiral phosphine catalyzed asymmetric Michael additions of N-Boc oxindoles was published online
    • Angew. Chem. Int. Ed. 2009, 48, 4559. Following our submission of this manuscript, a report from Lu and co-workers on chiral phosphine catalyzed asymmetric Michael additions of N-Boc oxindoles was published online
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4559
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    • DOI:; Angew. Chem. Int. Ed. 2012, DOI:). However, this method suffers from the same operational drawbacks mentioned (i.e. high dilution and cryogenic temperatures) and the singular example of an asymmetric addition into acrolein proceeds with more modest (71 %) ee.
    • F. Zhong, X. Dou, X. Han, W. Yao, Q. Zhu, Y. Meng, Y. Lu, Angew. Chem. 2012, DOI:; Angew. Chem. Int. Ed. 2012, DOI:). However, this method suffers from the same operational drawbacks mentioned (i.e. high dilution and cryogenic temperatures) and the singular example of an asymmetric addition into acrolein proceeds with more modest (71 %) ee.
    • (2012) Angew. Chem.
    • Zhong, F.1    Dou, X.2    Han, X.3    Yao, W.4    Zhu, Q.5    Meng, Y.6    Lu, Y.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.