A versatile synthetic methodology for the synthesis of tryptophols
SJ Garden, RB da Silva, AC Pinto
Index: Garden, Simon J; Da Silva, Rosangela B; Pinto, Angelo C Tetrahedron, 2002 , vol. 58, # 42 p. 8399 - 8412
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Citation Number: 64
Abstract
Tryptophols have been obtained in high yields by the reduction of 3-substituted-dioxindoles (obtained by the aldol condensation reaction of ketones with isatins or by a modified Knovenagel malonate condensation) using a borane tetrahydrofuran complex. The reported methodology offers distinct advantages over existing methods for the synthesis of these compounds, including consistently greater yields, diastereoselective syntheses and the ...
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