An asymmetric synthesis of the tricyclic core (−)-<b>1</b> of the marine diterpene bielschowskysin is described. In particular, a methodology was developed to introduce the crucial quaternary center at C-12
The regio- and stereoselective synthesis of the keto-esters 20 and 22 are described, the latter bein...
Chapter one provides a summary of efforts towards the syntheses of the welwitindolinones with bicycl...
The first total synthesis of a chromodorolide marine diterpenoid is described. The core of the diter...
A direct route for the synthesis of highly functionalized bicyclo[3.2.0]heptane core containing the ...
A novel approach towards bielschowskysin is reported based on an attempted stepwise cyclobutane form...
Diese Dissertation beschreibt die Arbeit an der Totalsynthese von Bielschowskysin. Bielschowskysin ...
The unique structure of furanocembranoid natural product bielschowskysin has provoked a number of bi...
Bielschowskysin (1), ein hoch oxygeniertes Furanocembranolid isoliert aus der gorgonischen Oktokoral...
The total synthesis and synthetic efforts towards several diterpene natural products are described. ...
A concise, (Z)-selective ring-closing metathesis (RCM) route to the 14-membered carbocycle of bielsc...
The formation of quaternary centers is a formidable challenge. Once these quaternary centers become ...
Thesis describes synthetic studies directed towards evaluating the biosynthetic relationships betwee...
Progress toward the cyclobutane core of bielshowskysin is reported. The core was thought to arise fr...
Enantiospecific construction of the bicyclo[4.3.0]nonan-8-one 17 employing a lithium and liquid ammo...
The synthesis of a bicyclo[2.2.l] heptane derivative 2 and its transformation to two different cyclo...
The regio- and stereoselective synthesis of the keto-esters 20 and 22 are described, the latter bein...
Chapter one provides a summary of efforts towards the syntheses of the welwitindolinones with bicycl...
The first total synthesis of a chromodorolide marine diterpenoid is described. The core of the diter...
A direct route for the synthesis of highly functionalized bicyclo[3.2.0]heptane core containing the ...
A novel approach towards bielschowskysin is reported based on an attempted stepwise cyclobutane form...
Diese Dissertation beschreibt die Arbeit an der Totalsynthese von Bielschowskysin. Bielschowskysin ...
The unique structure of furanocembranoid natural product bielschowskysin has provoked a number of bi...
Bielschowskysin (1), ein hoch oxygeniertes Furanocembranolid isoliert aus der gorgonischen Oktokoral...
The total synthesis and synthetic efforts towards several diterpene natural products are described. ...
A concise, (Z)-selective ring-closing metathesis (RCM) route to the 14-membered carbocycle of bielsc...
The formation of quaternary centers is a formidable challenge. Once these quaternary centers become ...
Thesis describes synthetic studies directed towards evaluating the biosynthetic relationships betwee...
Progress toward the cyclobutane core of bielshowskysin is reported. The core was thought to arise fr...
Enantiospecific construction of the bicyclo[4.3.0]nonan-8-one 17 employing a lithium and liquid ammo...
The synthesis of a bicyclo[2.2.l] heptane derivative 2 and its transformation to two different cyclo...
The regio- and stereoselective synthesis of the keto-esters 20 and 22 are described, the latter bein...
Chapter one provides a summary of efforts towards the syntheses of the welwitindolinones with bicycl...
The first total synthesis of a chromodorolide marine diterpenoid is described. The core of the diter...
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