A concise synthesis of a highly functionalized tricyclic ring system representing the CDE core of nortriterpenoid schintrilactones A and B is described using a tandem ROM-RCM of a norbornene derivative
A novel route for the synthesis of a highly functionalized lactarane skeleton in enantiomerically pu...
An efficient stereoselective approach to the construction of a hydrindane derivative having a bridge...
The addition of allyl magnesium and allyl indium reagents to a key TBS protected norbornenyl buildin...
Construction of 6/7 fused bicycles featuring C/D rings of micrandilactone C and rubrifloradilactone ...
A stereocontrolled approach for the construction of ABC ring systems of micrandilactone A and lancif...
Domino metathesis involving ROM-RCM of appropriately constructed norbornene derivatives having multi...
A general approach for the synthesis of fused cyclic systems containing medium-sized rings (7-9) has...
Full details of the total synthesis of the Schisandraceae nortriterpenoid natural product rubriflord...
First-generation synthetic strategies for the diastereoselective total synthesis of schindilactone A...
A conceptually unifying and flexible approach to the ABC and FGH segments of the nortriterpenoid rub...
Contains fulltext : 18989_syntanexo.pdf (publisher's version ) (Open Access)143 p
The successful synthesis of the highly complex model compound (2) of the CEFGH ring system of schind...
Rubriflordilactones A and B are highly oxygenated nortriterpenoid natural products isolated from Sc...
An enantioselective synthesis of the AB ring system common to the majority of the Schisandra nortrit...
A concise approach towards the synthesis of the highly biologically active terpenoid caribenol A is ...
A novel route for the synthesis of a highly functionalized lactarane skeleton in enantiomerically pu...
An efficient stereoselective approach to the construction of a hydrindane derivative having a bridge...
The addition of allyl magnesium and allyl indium reagents to a key TBS protected norbornenyl buildin...
Construction of 6/7 fused bicycles featuring C/D rings of micrandilactone C and rubrifloradilactone ...
A stereocontrolled approach for the construction of ABC ring systems of micrandilactone A and lancif...
Domino metathesis involving ROM-RCM of appropriately constructed norbornene derivatives having multi...
A general approach for the synthesis of fused cyclic systems containing medium-sized rings (7-9) has...
Full details of the total synthesis of the Schisandraceae nortriterpenoid natural product rubriflord...
First-generation synthetic strategies for the diastereoselective total synthesis of schindilactone A...
A conceptually unifying and flexible approach to the ABC and FGH segments of the nortriterpenoid rub...
Contains fulltext : 18989_syntanexo.pdf (publisher's version ) (Open Access)143 p
The successful synthesis of the highly complex model compound (2) of the CEFGH ring system of schind...
Rubriflordilactones A and B are highly oxygenated nortriterpenoid natural products isolated from Sc...
An enantioselective synthesis of the AB ring system common to the majority of the Schisandra nortrit...
A concise approach towards the synthesis of the highly biologically active terpenoid caribenol A is ...
A novel route for the synthesis of a highly functionalized lactarane skeleton in enantiomerically pu...
An efficient stereoselective approach to the construction of a hydrindane derivative having a bridge...
The addition of allyl magnesium and allyl indium reagents to a key TBS protected norbornenyl buildin...
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