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Volumn 65, Issue 6, 2000, Pages 1636-1642

On five- vs six-membered diacetal formation from threitol and the intermediacy of unusually stable protonated species

Author keywords

[No Author keywords available]

Indexed keywords

TETRAOXADECALIN; THREITOL; UNCLASSIFIED DRUG;

EID: 0034708657     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9908952     Document Type: Article
Times cited : (12)

References (35)
  • 2
    • 0343011957 scopus 로고    scopus 로고
    • note
    • (b) We use consistently the 1,3,5,7-tetraoxadecalin nomenclature. Other possible names are cis- or trans-2,4,7,9-tetraoxabicyclo[4.4.0]decane, 1,3:2,4-di-O-methylenethreitol, or (cf. CA) (4aR)-(4ar,8ac)-tetrahydro-[1,3]dioxino[5,4-d]-1,3-dioxm. Also, due to a minor but basic omission of the CIP rules, one can assign unequivocally configurations to chiral cis-decalin systems, only by 9,10-helicity designation, e.g., molecule 3c is (2R,6R,9R;9,10-M)-2,6- bis(bromomethyl)-cis-1,3,5,7-tetraoxadecalin.
  • 21
    • 0342915969 scopus 로고
    • Pigman, W., Horton, D., Eds.; Academic Press: New York, Ch. 11
    • (d) Foster, A. B. In The Carbohydrates; Pigman, W., Horton, D., Eds.; Academic Press: New York, 1972; Vol. 1A, Ch. 11.
    • (1972) The Carbohydrates , vol.1 A
    • Foster, A.B.1
  • 22
    • 0343883405 scopus 로고    scopus 로고
    • note
    • (e) Cf. ref 6e for a short but relevant review on carbohydrate TOD derivatives.
  • 23
    • 0343447557 scopus 로고    scopus 로고
    • note
    • (a) MM3 is available from QCPE (latest public version); the official distributors are Technical Utilization Corporation, Inc., 235 Glen Village Court, Powell, OH 43065, and Tripos Associates, 1699 S. Hanley Road, St. Louis, MO 63144.
  • 26
    • 0343447555 scopus 로고    scopus 로고
    • note
    • 6b is a reparametrized version for the gauche effect in O-C-C-O-containing systems.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.