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Volumn , Issue 9, 2005, Pages 1383-1388

Concave reagents, 45.1 2,6-Di-tert-butylpyridine-loaded dendrimers and their use in vinyl triflate synthesis

Author keywords

Base catalysis; Dendrimers; Recycling; Steric hindrance; Triflate

Indexed keywords

AROMATIC COMPOUNDS; DERIVATIVES; RECYCLING; SYNTHESIS (CHEMICAL);

EID: 20644442016     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-865355     Document Type: Article
Times cited : (3)

References (22)
  • 18
    • 0012440132 scopus 로고
    • As an intermediate, 2d has been described in the synthesis of 1,2-bis(2,6-di-tert-butylpyridinyl)ethane: Hou, C. J.; Okamoto, Y. J. Org. Chem. 1982, 47, 1977.
    • (1982) J. Org. Chem. , vol.47 , pp. 1977
    • Hou, C.J.1    Okamoto, Y.2
  • 19
    • 20644459433 scopus 로고    scopus 로고
    • note
    • + - 325] was detectable but did not match any fragments. Relative intensities did not change upon variation of the laser power. Possibly, impure dendrons have been used lacking one pyridine and one dihydroxybenzyl alcohol unit. In other batches using dendrons which had been purified by GPC, this impurity could be avoided.
  • 20
    • 20644455502 scopus 로고    scopus 로고
    • note
    • + - 325] signals could be detected (m/z = 3519), probably because the dendron contained the same impurity. Again, the impurity could be avoided when dendron 13 was purified by GPC.
  • 22
    • 20644458956 scopus 로고    scopus 로고
    • note
    • Sometimes the material had to be purified by GPC which lowered the yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.