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Diastereoselective synthesis of spirodihydrobenzofuran analogues of the natural product filifolinol
(Wiley, 2020)
Filifolinol is a natural occurring spirodihydrobenzofuran isolated from the resinous exudates of Heliotropium filifolium, a Chilean endemic shrub. Filifolinol and some of its derivatives have shown interesting biological ...
The influence of protecting groups on the diastereoselectivity of catalytic heterogeneous hydrogenation of Baylis-Hillman adducts
(Arkat Usa IncGainesvilleEUA, 2003)
Addition of a chiral boron enolate to cyclic N-acyliminium ions. Stereocontrolled synthesis of the pyrrolizidine ring system
(Amer Chemical SocWashington, 1996)
Diastereoselectivity in heterogeneous catalytic hydrogenation of Baylis-Hillman adducts. Total synthesis of (+/-)-sitophilate
(Pergamon-elsevier Science LtdOxfordInglaterra, 2001)
Diastereoselective epoxidation of allylic diols derived from Baylis-Hillman adducts
(Georg Thieme Verlag KgStuttgartAlemanha, 2005)
An approach to substituted dihydroisoquinolin-1(2H)-ones from Baylis-Hillman adducts
(Pergamon-elsevier Science LtdOxfordInglaterra, 2003)
Diastereoselective synthesis of 2,5-disubstituted tetrahydrofuran derivatives
(Pergamon-elsevier Science LtdOxfordInglaterra, 2000)
Regio- and diastereoselective synthesis of 5-trans-substituted and 5,5-disubstituted 2-pyrrolidinones derived from (S)-malic acid
(Pergamon-elsevier Science LtdOxfordInglaterra, 2002)