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- W4251619386 abstract "Komplementäre Diastereoselektivität wurde mit Dihalogen- und Dialkylcarbenen bei der Cyclopropanierung von 1 beobachtet (Weg a bzw. b). Die Umwandlung von 1 in 7,7-Dimethylbicyclo[4.1.0]heptan-1,2-diole (±)-2 und (±)-3 ist der entscheidende Schritt der hier vorgestellten Strategie, die auf die Synthese von Phorbolderivaten abzielt. TBDMS=tert-Butyldimethylsilyl." @default.
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- W4251619386 date "2001-06-18" @default.
- W4251619386 modified "2023-10-16" @default.
- W4251619386 title "Diastereocontrol in the Synthesis of Models of Rings C and D of Phorbol: Directing Effect of an Ether Substituent on Lithium Carbenoid Mediated Cyclopropanation" @default.
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- W4251619386 doi "https://doi.org/10.1002/1521-3757(20010618)113:12<2373::aid-ange2373>3.0.co;2-5" @default.
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