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Volumn 2, Issue 18, 2004, Pages 2555-2557

Cross-metathesis coupling of sugars and fatty acids to lysine and cysteine

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; ANTIBODIES; BIOSYNTHESIS; CATALYSTS; COLUMN CHROMATOGRAPHY; COOLING; DIMERS; ETHYLENE; FATTY ACIDS; NITROGEN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OPTIMIZATION; PROTEINS; SUGARS;

EID: 4744364085     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b411770k     Document Type: Article
Times cited : (18)

References (22)
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    • In recent times cross metathesis (CM) has emerged as an important, and general synthetic reaction, in which alkyl groups from two different substrates are coupled to give a new olefin. see A. J. Vernall and A. D. Abell, Aldrichimica Acta, 2003, 36, 93; S. J. Connon and S. Blechert, Angew. Chem., Int. Ed., 2003, 42, 1900; H. E. Blackwell, D. J. O'Leary, A. K. Chatterjee, R. A. Washenfelder, D. A. Bussmann and R. H. Grubbs, J. Am. Chem. Soc., 2000, 122, 58.
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  • 10
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    • In recent times cross metathesis (CM) has emerged as an important, and general synthetic reaction, in which alkyl groups from two different substrates are coupled to give a new olefin. see A. J. Vernall and A. D. Abell, Aldrichimica Acta, 2003, 36, 93; S. J. Connon and S. Blechert, Angew. Chem., Int. Ed., 2003, 42, 1900; H. E. Blackwell, D. J. O'Leary, A. K. Chatterjee, R. A. Washenfelder, D. A. Bussmann and R. H. Grubbs, J. Am. Chem. Soc., 2000, 122, 58.
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    • In recent times cross metathesis (CM) has emerged as an important, and general synthetic reaction, in which alkyl groups from two different substrates are coupled to give a new olefin. see A. J. Vernall and A. D. Abell, Aldrichimica Acta, 2003, 36, 93; S. J. Connon and S. Blechert, Angew. Chem., Int. Ed., 2003, 42, 1900; H. E. Blackwell, D. J. O'Leary, A. K. Chatterjee, R. A. Washenfelder, D. A. Bussmann and R. H. Grubbs, J. Am. Chem. Soc., 2000, 122, 58.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 58
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    • T. D. Perrine, C. P. J. Glaudemans, R. K. Ness, J. Kyle and H. G. Fletcher Jr., J. Org. Chem., 1967, 32, 664; R. P. Spencer, C. L. Cavallaro and J. Schwartz, J. Org. Chem., 1999, 64, 3987; E. Brenna, C. Fuganti, P. Grasselli, S. Serra and S. Zambotti, Chem. Eur. J., 2002, 8, 1872.
    • (1967) J. Org. Chem. , vol.32 , pp. 664
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    • T. D. Perrine, C. P. J. Glaudemans, R. K. Ness, J. Kyle and H. G. Fletcher Jr., J. Org. Chem., 1967, 32, 664; R. P. Spencer, C. L. Cavallaro and J. Schwartz, J. Org. Chem., 1999, 64, 3987; E. Brenna, C. Fuganti, P. Grasselli, S. Serra and S. Zambotti, Chem. Eur. J., 2002, 8, 1872.
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    • T. D. Perrine, C. P. J. Glaudemans, R. K. Ness, J. Kyle and H. G. Fletcher Jr., J. Org. Chem., 1967, 32, 664; R. P. Spencer, C. L. Cavallaro and J. Schwartz, J. Org. Chem., 1999, 64, 3987; E. Brenna, C. Fuganti, P. Grasselli, S. Serra and S. Zambotti, Chem. Eur. J., 2002, 8, 1872.
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    • note
    • 1H NMR.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.