메뉴 건너뛰기




Volumn 73, Issue 14, 2008, Pages 5592-5594

Electrophile-induced ether transfer: Stereoselective synthesis of 2,6-disubstituted-3,4-dihydropyrans

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; ETHERS; ORGANIC COMPOUNDS; STEREOCHEMISTRY; STEREOSELECTIVITY;

EID: 48249132008     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800704d     Document Type: Article
Times cited : (21)

References (48)
  • 16
    • 0035936738 scopus 로고    scopus 로고
    • Other established strategies for the preparation of glycals: (a) Rainier, J. D.; Allwein, S. P.; Cox, J. M. J. Org. Chem. 2001, 66, 1380.
    • Other established strategies for the preparation of glycals: (a) Rainier, J. D.; Allwein, S. P.; Cox, J. M. J. Org. Chem. 2001, 66, 1380.
  • 18
    • 0000645983 scopus 로고    scopus 로고
    • Recent reviews in Ferrier Rearrangement: Ferrier, R. J
    • Recent reviews in Ferrier Rearrangement: Ferrier, R. J. Top. Curr. Chem. 2001, 215, 153.
    • (2001) Top. Curr. Chem , vol.215 , pp. 153
  • 19
    • 48249085977 scopus 로고    scopus 로고
    • The 2,6-trans stereoconfiguration of dihydropyran 5a and 5h were unambigously assigned based on ROESY experiment.
    • The 2,6-trans stereoconfiguration of dihydropyran 5a and 5h were unambigously assigned based on ROESY experiment.
  • 22
    • 33748726149 scopus 로고    scopus 로고
    • Ley and co-workers have demonstrated similar Ferrier rearrangement using a tertiary allylic ether for the construction of the spiroketal moiety in okadaic acid: Ley, S. V, Humphries, A. C, Eick, H, Downham, R, Ross, A. R, Boyce, R. J, Pavey, J. B. J, Pietruszka, J. J. Chem. Soc, Perkin Trans.1 1998, 3907
    • Ley and co-workers have demonstrated similar Ferrier rearrangement using a tertiary allylic ether for the construction of the spiroketal moiety in okadaic acid: Ley, S. V.; Humphries, A. C.; Eick, H.; Downham, R.; Ross, A. R.; Boyce, R. J.; Pavey, J. B. J.; Pietruszka, J. J. Chem. Soc., Perkin Trans.1 1998, 3907.
  • 23
    • 48249124836 scopus 로고    scopus 로고
    • 1H NMR coupling-constant analysis.
    • 1H NMR coupling-constant analysis.
  • 26
    • 0028306861 scopus 로고    scopus 로고
    • Nicolaou's total synthesis of swinholide A: (a) Patron, A. P.; Richter, P. K.; Tomaszewski, M. J.; Miller, R. A.; Nicolaou, K. C. J. Chem. Soc., Chem. Commun. 1994, 1147.
    • Nicolaou's total synthesis of swinholide A: (a) Patron, A. P.; Richter, P. K.; Tomaszewski, M. J.; Miller, R. A.; Nicolaou, K. C. J. Chem. Soc., Chem. Commun. 1994, 1147.
  • 30
    • 0026681175 scopus 로고    scopus 로고
    • Paterson's total synthesis of swinholide A: (a) Paterson, I.; Cumming, J. Tetrahedron Lett. 1992, 33, 2847.
    • Paterson's total synthesis of swinholide A: (a) Paterson, I.; Cumming, J. Tetrahedron Lett. 1992, 33, 2847.
  • 41
    • 0028132030 scopus 로고    scopus 로고
    • Nakata's synthetic approach to preswinholide A: (a) Nakata, T.; Komatsu, T.; Nagasawa, K. Chem. Rev. Bull. 1994, 42, 2403.
    • Nakata's synthetic approach to preswinholide A: (a) Nakata, T.; Komatsu, T.; Nagasawa, K. Chem. Rev. Bull. 1994, 42, 2403.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.