메뉴 건너뛰기




Volumn 34, Issue 8, 1995, Pages 909-912

A Highly Stereoselective Synthesis of 1,2‐trans‐C‐Glycosides via Glycosyl Samarium(III) Compounds

Author keywords

aldehydes; asymmetric syntheses; C glycosides; ketones; samarium compounds

Indexed keywords


EID: 33748974766     PISSN: 05700833     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.199509091     Document Type: Article
Times cited : (102)

References (53)
  • 15
    • 0028267370 scopus 로고
    • Preferred conformation of C-glycosides. 12. Synthesis and conformational analysis of .alpha.,.alpha.-, .alpha.,.beta.-, and .beta.,.beta.-C-trehaloses
    • 88–96 and previous work
    • (1994) The Journal of Organic Chemistry , vol.59
    • Wei, A.1    Kishi, Y.2
  • 49
    • 84985539475 scopus 로고    scopus 로고
    • 3, 4 = 2.8–4.0 Hz.
  • 50
    • 84985621312 scopus 로고    scopus 로고
    • 1, 7 = 7.8 Hz.
  • 51
    • 84985525433 scopus 로고    scopus 로고
    • The anomeric composition of the C‐glycosides derived from sulfone 24 was determined by derivatization to their corresponding imidazole thiocarbamates and chromatographic separation. Unfortunately, the composition of the C‐7 diastereomers could not be determined due to the trifluoroacetamido group giving rise to rotameric mixtures.
  • 52
    • 84985509407 scopus 로고
    • Compound 26 was obtained by NIS‐assisted iodoglycosylation (, Synthesis, 696–698) of tri‐O‐benzyl‐D‐glucal with racemic 1‐phenyl‐3‐propenol [19].
    • (1978)
    • Thiem, J.1    Karl, H.2    Schwenter, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.