Add to ORKGThe Diels-Alder cycloaddition reactions of a small selection of transient C-nitroso compounds (two achiral and one chiral) were carried out with the unsymmetrically substituted, conjugated diene (E)-penta-1,3-diene 111 (piperylene). The aim of these experiments was to study the regiochemistry and any associated asymmetric induction of the cycloadducts. Acetohydroxamic acid 182d was oxidized, with periodate, in the presence of (E)-penta-1,3-diene 111 at
The Diels-Alder reaction was discovered in 1928 and has become the most efficient and practical met...
Regioselectivity in Diels-Alder reactions is usually explained using frontier molecular orbital and/...
Abstract: Diels-Alder reactions have emerged as highly powerful transformations for the generation o...
The Diels-Alder cycloaddition reactions of a small selection of transient C-nitroso compounds (two a...
Oxidation of hydroxamic acids, and also related N-hydroxyureas and N-hydroxycarbamates, gives acylni...
Oxidation of (+/-)-mandelohydroxamic acid (328a) with periodate gave the corresponding transient C. ...
Oxidation of hydroxamic acids, and also related N-hydroxyureas and N-hydroxycarbamates, gives acylni...
Asymmetric Diels-Alder reactions of 2-(trimethylsilyloxy)cyclohexa-1,3-diene 17a, 6,6-dimethyl-2-(tr...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
Diene 2b reacted regioselectively with dienophiles. Adduct 6 was converted into the left-hand portio...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
The cycloaddition reactions between nitronaphthalenes and 1-trimethylsilyloxy-1,3-butadiene produce ...
The Diels-Alder reaction was discovered in 1928 and has become the most efficient and practical met...
Regioselectivity in Diels-Alder reactions is usually explained using frontier molecular orbital and/...
Abstract: Diels-Alder reactions have emerged as highly powerful transformations for the generation o...
The Diels-Alder cycloaddition reactions of a small selection of transient C-nitroso compounds (two a...
Oxidation of hydroxamic acids, and also related N-hydroxyureas and N-hydroxycarbamates, gives acylni...
Oxidation of (+/-)-mandelohydroxamic acid (328a) with periodate gave the corresponding transient C. ...
Oxidation of hydroxamic acids, and also related N-hydroxyureas and N-hydroxycarbamates, gives acylni...
Asymmetric Diels-Alder reactions of 2-(trimethylsilyloxy)cyclohexa-1,3-diene 17a, 6,6-dimethyl-2-(tr...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
Diene 2b reacted regioselectively with dienophiles. Adduct 6 was converted into the left-hand portio...
At the beginning of the reseach described in this thesis the catalytic asymmetric Diels-Alder reacti...
The cycloaddition reactions between nitronaphthalenes and 1-trimethylsilyloxy-1,3-butadiene produce ...
The Diels-Alder reaction was discovered in 1928 and has become the most efficient and practical met...
Regioselectivity in Diels-Alder reactions is usually explained using frontier molecular orbital and/...
Abstract: Diels-Alder reactions have emerged as highly powerful transformations for the generation o...