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Total synthesis of dl-cephalotaxine. The first example of an intramolecular 4 + 2 cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety.

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Title: Total synthesis of dl-cephalotaxine. The first example of an intramolecular 4 + 2 cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety.
Authors: Burkholder, T. P., Fuchs, P. L.
Source: Journal of the American Chemical Society; March 30 1988, Vol. 110, p2341-2342, 2p
Database: Applied Science & Technology Source
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DbLabel: Applied Science & Technology Source
An: 501976126
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PubType: Academic Journal
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  Data: Total synthesis of dl-cephalotaxine. The first example of an intramolecular 4 + 2 cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety.
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+the+American+Chemical+Society%22">Journal of the American Chemical Society</searchLink>; March 30 1988, Vol. 110, p2341-2342, 2p
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      – Code: eng
        Text: English
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      – TitleFull: Total synthesis of dl-cephalotaxine. The first example of an intramolecular 4 + 2 cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety.
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              Text: March 30 1988
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              Y: 1988
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