An economical diels-alder strategy for the synthesis of daphniphyllum alkaloids
J Orban, JV Turner
Index: Orban, John; Turner, John V. Tetrahedron Letters, 1983 , vol. 24, # 26 p. 2697 - 2700
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Citation Number: 21
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... A convergent and essentially self-consistent strategy, featuring an unusual Diels-Alder reaction has been devised for the stereo-controlled synthesis of a logical tetracyclic precursor 21 to daphniphyllum alkaloids. ... The possibility of utilizing a 6-isopropyl analogue of 5, derived from a chiral ...
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