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Volumn 25, Issue 5, 1984, Pages 569-572

A new synthesis of N-benzoyl L-acosamine

Author keywords

[No Author keywords available]

Indexed keywords

DRUG ANALYSIS; DRUG IDENTIFICATION; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROMETRY; N BENZOYLACOSAMINE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; POLARIMETRY; PRELIMINARY COMMUNICATION; THEORETICAL STUDY;

EID: 0021336840     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)99940-4     Document Type: Article
Times cited : (27)

References (29)
  • 12
    • 84918427668 scopus 로고    scopus 로고
    • All the new compounds gave satisfactory spectral and analytical data.
  • 14
    • 2042432431 scopus 로고
    • Bis[trimethylsilyl] Sulfate-Catalyzed Alcohol Protection with Dihydropyran, Deprotection, and Transesterification
    • Conventional protic or Lewis acid catalysts gave complex mixture of products. As to the acid catalysis of bis(trimethylsilyl) sulfate, see:
    • (1981) Synthesis , pp. 899
    • Morizawa1    Mori2    Hiyama3    Nozaki4
  • 16
    • 84918427667 scopus 로고    scopus 로고
    • 3N) (83% yield). In a similar way we prepared (2S,3S)-2,3-(2′,2′-propylidenedioxy)butanenitrile also.
  • 19
    • 84918427666 scopus 로고    scopus 로고
    • 3 in carbon tetrachloride to give two doublets at δ 4.46 and 4.50. The optically active sample gave the former peak only within the error of 5%.
  • 27
    • 84918427665 scopus 로고    scopus 로고
    • 2 hydrogen pressure in ethyl acetate with complete stereocontrol, it took much longer reaction time.
  • 28
    • 0013507745 scopus 로고
    • The high stereoselectivity may be attributed to the steric bulk of the dioxolane ring as well as the orbital effect of the allylic alkoxy group as discussed in
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 1106
    • Franck1    John2    Olejniczak3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.