Abstract
The case history of achiral cantharidin reveals the development of unusual conditions under which the Diels/Alder reaction can play the key synthetic part.
The case history of chiral (-)-norgestrel demonstrates that the Diels/Alder reaction is going to become one of the best controllable structural transformations for enantioselective generation of molecular chirality through catalysis. There are, however, standard syntheses without a Diels/Alder reaction known.
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Quinkert, G., del Grosso, M. (1994). Progress in the Diels/Alder Reaction Means Progress in Steroid Synthesis. In: Ottow, E., Schöllkopf, K., Schulz, BG. (eds) Stereoselective Synthesis. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-78496-5_6
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DOI: https://doi.org/10.1007/978-3-642-78496-5_6
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