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Volumn 10, Issue 6, 2008, Pages 1039-1042

Homogeneous pd-catalyzed enantioselective decarboxylative protonation

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID; PALLADIUM; PROTON;

EID: 45549100093     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702821j     Document Type: Article
Times cited : (69)

References (40)
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    • (c) Yanagisawa, A.; Yamamoto, H. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: New York, 1999; Vol. 3, pp 1295-1306.
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    • Yanagisawa, A.1    Yamamoto, H.2
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    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: New York
    • (d) Yanagisawa, A.; Yamamoto, H. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: New York, 2004; Supplement 2, pp 125-132.
    • (2004) Comprehensive Asymmetric Catalysis , Issue.SUPPL.EMENT 2 , pp. 125-132
    • Yanagisawa, A.1    Yamamoto, H.2
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    • 58149165762 scopus 로고    scopus 로고
    • For recent representative examples of enantioselective protonation, see
    • For recent representative examples of enantioselective protonation, see:
  • 21
    • 36949022498 scopus 로고    scopus 로고
    • and references therein. For a review of these enantioselective allylation reactions developed by our lab and others, see
    • For a review of these enantioselective allylation reactions developed by our lab and others, see: Mohr, J. T.; Stoltz, B. M. Chem. Asian J. 2007, 2, 1476-1491 and references therein.
    • (2007) Chem. Asian J , vol.2 , pp. 1476-1491
    • Mohr, J.T.1    Stoltz, B.M.2
  • 22
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    • For the development of phosphinooxazoline ligands, see
    • For the development of phosphinooxazoline ligands, see:
  • 24
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    • and references therein
    • Williams, J. M. J. Synlett 1996, 705-710 and references therein.
    • (1996) Synlett , pp. 705-710
    • Williams, J.M.J.1
  • 25
    • 34547164363 scopus 로고    scopus 로고
    • We have recently reported a convenient general synthetic route to PHOX ligands, see: Tani, K, Behenna, D. C, McFadden, R. M, Stoltz, B. M. Org. Lett. 2007, 9, 2529-2531
    • We have recently reported a convenient general synthetic route to PHOX ligands, see: Tani, K.; Behenna, D. C.; McFadden, R. M.; Stoltz, B. M. Org. Lett. 2007, 9, 2529-2531.
  • 27
    • 58149162437 scopus 로고    scopus 로고
    • To our knowledge, there are three other groups that have reported related Pd-catalyzed systems that produce similar enantioenriched products
    • To our knowledge, there are three other groups that have reported related Pd-catalyzed systems that produce similar enantioenriched products.
  • 35
    • 0000823558 scopus 로고
    • For the initial synthesis of this compound, see
    • (a) For the initial synthesis of this compound, see: Meldrum, A. N. J. Chem. Soc. 1908, 93, 598-601.
    • (1908) J. Chem. Soc , vol.93 , pp. 598-601
    • Meldrum, A.N.1
  • 36
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    • For the correct structural assignment, see
    • (b) For the correct structural assignment, see: Davidson, D.; Bernhard, S. A. J. Am. Chem. Soc. 1948, 70, 3426-3428.
    • (1948) J. Am. Chem. Soc , vol.70 , pp. 3426-3428
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    • For a highlight of recent chemistry based on Meldrum's acid, see
    • (c) For a highlight of recent chemistry based on Meldrum's acid, see: Bonifácia, V. D. B. Synlett 2004, 1649-1650.
    • (2004) Synlett , pp. 1649-1650
    • Bonifácia, V.D.B.1
  • 38
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    • See the Supporting Information for details
    • See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.