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Volumn 47, Issue 32, 2006, Pages 5785-5788

Regio- and stereoselective synthesis of methyl 5-methylenetetrahydropyran-3-carboxylates from Baylis-Hillman adducts via allyltributylstannane-mediated radical cyclization

Author keywords

Allyltributylstannane; Methylenetetrahydropyran; Radical cyclization; Regioselective; Stereoselective

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; TIN DERIVATIVE;

EID: 33745615627     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.05.186     Document Type: Article
Times cited : (32)

References (23)
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    • Trost B.M., and Fleming I. (Eds), Pergamon Press, Oxford
    • Knochel P. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 4 (1991), Pergamon Press, Oxford 865-911
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 865-911
    • Knochel, P.1
  • 3
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    • Trost B.M., and Fleming I. (Eds), Pergamon Press, Oxford
    • Fleming I. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 2 (1991), Pergamon Press, Oxford 563-593
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 563-593
    • Fleming, I.1
  • 4
    • 0033583167 scopus 로고    scopus 로고
    • Lewis acid or metal-catalyzed allylstannylation of alkynes, see:
    • Lewis acid or metal-catalyzed allylstannylation of alkynes, see:. Matsukawa Y., Asao N., Kitahara H., and Yamamoto Y. Tetrahedron 55 (1999) 3779
    • (1999) Tetrahedron , vol.55 , pp. 3779
    • Matsukawa, Y.1    Asao, N.2    Kitahara, H.3    Yamamoto, Y.4
  • 8
    • 0034680577 scopus 로고    scopus 로고
    • For the examples of allylstannylation of alkynes, see:
    • For the examples of allylstannylation of alkynes, see:. Miura K., Saito H., Fujisawa N., and Hosomi A. J. Org. Chem. 65 (2000) 8119
    • (2000) J. Org. Chem. , vol.65 , pp. 8119
    • Miura, K.1    Saito, H.2    Fujisawa, N.3    Hosomi, A.4
  • 13
    • 17144366548 scopus 로고    scopus 로고
    • and many references were cited on the importance of suitably substituted tetrahydropyran derivatives. Further references on the radical cyclization of modified Baylis-Hillman adducts were cited in Refs. 6 and 9
    • Shanmugam P., and Rajasingh P. Synlett (2005) 939 and many references were cited on the importance of suitably substituted tetrahydropyran derivatives. Further references on the radical cyclization of modified Baylis-Hillman adducts were cited in Refs. 6 and 9
    • (2005) Synlett , pp. 939
    • Shanmugam, P.1    Rajasingh, P.2
  • 14
    • 33745584516 scopus 로고    scopus 로고
    • note
    • ++1).
  • 16
    • 33745608355 scopus 로고    scopus 로고
    • note
    • ++1).
  • 17
    • 0035862638 scopus 로고    scopus 로고
    • For the regioselectivity during radical cyclization, see:
    • For the regioselectivity during radical cyclization, see:. Della E., and Smith P.A. Tetrahedron Lett. 42 (2001) 481
    • (2001) Tetrahedron Lett. , vol.42 , pp. 481
    • Della, E.1    Smith, P.A.2
  • 20
    • 17244374220 scopus 로고    scopus 로고
    • Radical cyclization in Baylis-Hillman chemistry, see:
    • Radical cyclization in Baylis-Hillman chemistry, see:. Shanmugam P., and Rajasingh P. Tetrahedron Lett. 46 (2005) 3369
    • (2005) Tetrahedron Lett. , vol.46 , pp. 3369
    • Shanmugam, P.1    Rajasingh, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.