Synthesis of novel macrocyclic compounds utilizing characteristic bonding properties of hypervalent sulfur

Heterocycles

Volumn 53, Issue 6, 2000, Pages 1239-1245

  Matsumura, Noboru ^b   Konishi, Tsunao ^b   Hayashi, Hirokazu ^b   Yasui, Masanori ^a   Iwasaki, Fujiko ^a   Mizuno, Kazuhiko ^b  

^a UNIVERSITY OF ELECTRO COMMUNICATIONS   (Japan)

^b Osaka Prefecture University   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MACROCYCLIC COMPOUND; SULFUR;

ARTICLE; CHEMICAL STRUCTURE; JAPAN; MOLECULAR INTERACTION; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 0034210215     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-00-8873     Document Type: Article

References (16)

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14. 4: C, 62.02; H, 8.43; N, 13.78; Found: C, 61.75; H, 8.52; N, 13.59.
15. 2= 0.393 (315 variables). The terminal three atoms of alkyl chain and solvent molecules are disordered, so that R factors were not sufficientry reduced. The backbone structure, however, was obtained from the direct method followed by successive Fourier syntheses. Details of X-Ray structure will be published elsewhere by F. Iwasaki, M. Yasui, and N. Matsumura.
16. C. K. Johnson, ORTEPII, Report OLNL-5138, Oak Ridge National Laboratory, Oak Ridge, TN, 1976.