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Volumn , Issue 24, 2006, Pages 2610-2612

The o-xylylene protecting group as an element of conformational control of remote stereochemistry in the synthesis of spiroketals

Author keywords

[No Author keywords available]

Indexed keywords

DISACCHARIDE; ETHER DERIVATIVE; O XYLYLENE ETHER; TRICYCLIC SPIRODISACCHARIDE; UNCLASSIFIED DRUG;

EID: 33745192842     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b604718a     Document Type: Article
Times cited : (22)

References (40)
  • 6
    • 0033580904 scopus 로고    scopus 로고
    • For selected references on the synthesis of spirooligosaccharides, see:
    • M. A. Brimble F. A. Farès Tetrahedron 1999 55 7661 7706
    • (1999) Tetrahedron , vol.55 , pp. 7661-7706
    • Brimble, M.A.1    Farès, F.A.2
  • 37
    • 2942708001 scopus 로고    scopus 로고
    • A complementary approach consisting of preforming the ketal centre and using it for remote control of the stereochemistry of spirocyclization reactions has been reported. See:
    • J. M. Benito E. M. Rubio M. Gómez-García C. Ortiz Mellet J. M. García Fernández Tetrahedron 2004 60 5899
    • (2004) Tetrahedron , vol.60 , pp. 5899
    • Benito, J.M.1    Rubio, E.M.2    Gómez-García, M.3    Ortiz, M.C.4    García, M.F.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.