메뉴 건너뛰기




Volumn 61, Issue 14, 2005, Pages 3497-3506

Achievement of ring inversion of myo-inositol derivatives due to silyloxy/silyloxy repulsion enhanced by the trans-substituents on both sides

Author keywords

Axial rich chair; Myo inositol; Ring conformation; Silyl protecting groups

Indexed keywords

1,2,3,6 TETRA O BENZYL 4,5 BIS O TERT BUTYLDIPHENYLSILYL INOSITOL; 4,5 BIS O TERT BUTYLDIPHENYLSILYL INOSITOL; 4,5 BIS O TRIISOPROPYLSILYL INOSITOL; CYCLOHEXANE; INOSITOL DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 14844340577     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.01.124     Document Type: Article
Times cited : (15)

References (36)
  • 24
    • 85030812593 scopus 로고    scopus 로고
    • note
    • Hydrogenation of 3p afforded 2-O-benzyl-3,4-bis-O-TBDPS-myo-inositol in 24% yield along with the full debenzylated 3.
  • 26
    • 85030814303 scopus 로고    scopus 로고
    • note
    • For the consistency with the numbering of the compounds, the numbering of 1-3, 4p-6p, 10, and 12 do not follow the IUPAC guidelines.
  • 29
    • 8544261103 scopus 로고    scopus 로고
    • Recently, a stable axial-rich chair form of the glucopyranose ring induced by the adjacent trans-OTBS groups has been produced. The ring-inversion of this compound would be caused by the enhanced steric hindrance of the OTBS/OTBS groups and also by the anomeric effect: H. Yamada, K. Tanigakiuchi, K. Nagao, K. Okajima, and T. Mukae Tetrahedron Lett. 45 2004 9207 9209
    • (2004) Tetrahedron Lett. , vol.45 , pp. 9207-9209
    • Yamada, H.1    Tanigakiuchi, K.2    Nagao, K.3    Okajima, K.4    Mukae, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.