Add to ORKG3 pagesA synthesis of the C1-C15 fragment of Dolabelide C is reported. The key step is a diastereoselective Mukaiyama aldol reaction to form the C6-C7 bond, followed by reduction and deoxygenation of the carbonyl group at C5. The trisubstituted vinyl iodide is introduced via the corresponding vinyl boronate by cross-metathesis
A flexible synthesis of the C1-C12 fragment of Tedanolide C has been accomplished in eight steps fro...
This thesis deals with the development of new reaction methodology for stereoselective synthesis, as...
Mukaiyama aldol, Mannich, and Michael reactions are arguably amongst the most important C–C bond for...
3 pagesA synthesis of the C1-C15 fragment of Dolabelide C is reported. The key step is a diastereose...
A highly demanding cross-metathesis (CM) reaction for the formation of the C24–C25 trisubstituted ol...
International audienceA highly demanding cross-metathesis (CM) reaction for the formation of the C24...
An efficient and highly stereoselective asymmetric synthesis of C1-C9 and C9-C17 fragments of (+)-13...
Let's talk about six! A new chiral disulfonimide catalyzed vinylogous Mukaiyama aldol addition of cr...
In der vorliegenden Arbeit wird die erste Totalsynthese des marinen Naturstoffs Dolabelid B beschrie...
International audience(Equation Presented) We have designed a new method to make synthons encompassi...
A convergent synthesis of the protected C(1)–C(11) fragment <b>6</b> of the targeted enantiomer of t...
Synthesis of the C1–C6 and C7–C23 fragments of the proposed structure of iriomoteolide 1a has been a...
A new family of cytotoxic macrolactones, dolabelides, was isolated from the sea hare Dolabella auric...
A stereoselective synthesis of the C1–C9 fragment of (–)-dictyostatin has been achieved by use of a ...
An organocatalyzed method for synthesizing chiral γ,γ-disubstituted γ-butenolides via direct vinylog...
A flexible synthesis of the C1-C12 fragment of Tedanolide C has been accomplished in eight steps fro...
This thesis deals with the development of new reaction methodology for stereoselective synthesis, as...
Mukaiyama aldol, Mannich, and Michael reactions are arguably amongst the most important C–C bond for...
3 pagesA synthesis of the C1-C15 fragment of Dolabelide C is reported. The key step is a diastereose...
A highly demanding cross-metathesis (CM) reaction for the formation of the C24–C25 trisubstituted ol...
International audienceA highly demanding cross-metathesis (CM) reaction for the formation of the C24...
An efficient and highly stereoselective asymmetric synthesis of C1-C9 and C9-C17 fragments of (+)-13...
Let's talk about six! A new chiral disulfonimide catalyzed vinylogous Mukaiyama aldol addition of cr...
In der vorliegenden Arbeit wird die erste Totalsynthese des marinen Naturstoffs Dolabelid B beschrie...
International audience(Equation Presented) We have designed a new method to make synthons encompassi...
A convergent synthesis of the protected C(1)–C(11) fragment <b>6</b> of the targeted enantiomer of t...
Synthesis of the C1–C6 and C7–C23 fragments of the proposed structure of iriomoteolide 1a has been a...
A new family of cytotoxic macrolactones, dolabelides, was isolated from the sea hare Dolabella auric...
A stereoselective synthesis of the C1–C9 fragment of (–)-dictyostatin has been achieved by use of a ...
An organocatalyzed method for synthesizing chiral γ,γ-disubstituted γ-butenolides via direct vinylog...
A flexible synthesis of the C1-C12 fragment of Tedanolide C has been accomplished in eight steps fro...
This thesis deals with the development of new reaction methodology for stereoselective synthesis, as...
Mukaiyama aldol, Mannich, and Michael reactions are arguably amongst the most important C–C bond for...