Original Article: Wang, Z.-G; Warren, J. D.; Dudkin, V. Y.; Zhang, X.; Iserloh, U.; Visser, M.; Eckhardt, M.; Seeberger, P. H.; Danishefsky, S. J. Tetrahedron 2006, 62, 4954-4978.
1.
Danishefsky, S. J.; Behar, V.; Randolph, J. T.; Lloyd, K. O. J. Am. Chem. Soc. 1995, 117, 5701-5711.
Reaction of 8 with dimethyldioxirane, followed by opening of the epoxide with allyl alcohol, followed by deacetylation with catayltic methoxide, led to pentasaccharide 9.
A.
Dumas, C.; Schibli, R.; Schubiger, P. A. J. Org. Chem. 2003, 68, 512-518.
In the the second paper, 1 was treated with m-CPBA in methanol to form 2 in 64% yield as described in Danishefsky article.
B.
Spassova, M. K.; Bornmann, W. G.; Ragupathi, G.; Sukenick, G.; Livingston, P. O.; Danishefsky, S. J. J. Org. Chem. 2005, 70, 3383-3395.
This author uses fucosylation reaction to synthesize big molecules.
C.
Tanaka, H.; Matoba, N.; Takahashi, T. Chemistry Letters 2005, 34, 400-401.
2.
Frick, W.; Bauer, A.; Bauer, S.; Wied, S.; Muller, G. Biochem. 1998, 37, 13421
3.
Iserloh, U.; Dudkin, V.; Wang, Z.-G.; Danishefsky, S. J. Tetrahedron Lett. 2002, 43, 7027-7030.
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