Regioselective introduction of two boronic acid groups into [60]fullerene using saccharides as imprinting templates

Chemical Communications

Volumn , Issue 9, 1998, Pages 1047-1048

  Ishi i, Tsutomu ^a   Nakashima, Kazuaki ^a   Shinkai, Seiji ^a  

^a JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 21844461555     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a801648h     Document Type: Article

References (17)

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12. 11B NMR spectroscopic and X-ray crystallographic studies it was found that in 6 boronic acids react with 1,3-diols to form two six-membered rings, and in 8 the saccharide moiety adopts the furanose form. These results will be discussed in detail elsewhere.
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17. 1H NMR spectrum, the out-in and out-out isomers can be excluded. Thus, 12a isolated here is the in-in isomer. For an explanation of the concept of in-in, out-in and out-out isomers, see refs. 4-6.