Beilstein J. Org. Chem.2008,4, No. 30, doi:10.3762/bjoc.4.30
catalytic amount of (EtO)3PCuI , TLC (ethyl acetate/n-hexane 1:1) revealed the formation of one faster moving product along with a complex mixture of slower moving products with mobility similar to those previously observed. Careful inspection of the products revealed that dimerisation of 4a occurred
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Graphical Abstract
Figure 1:
Schematic representation of glycosylated building blocks for the combinatorial synthesis of glycope...
Beilstein J. Org. Chem.2007,3, No. 45, doi:10.1186/1860-5397-3-45
by subsequent modifications of the experimental procedure.
We therefore returned our attention to the reduction of S-alkylxanthates that sometimes led to poor or irreproducible results when Method A was employed. In particular, some dimerisation of the radical generated from the xanthate was
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Graphical Abstract
Figure 1:
Reaction of α-acylxanthate 1a with 1-decene and Et3B/air.