Herein we describe synthetic efforts toward the total synthesis of calyciphylline B-type alkaloids. In the process, we disclose a detailed DFT study of equilibrium geometries and transition states that explains the stereochemical outcome during the formation of critical intermediates. X-ray crystallographic analysis reveals interesting conformational features in the naturally occurring deoxycalyciphylline B and its synthetic congeners
A stereochemically controlled route to the enantiopure [6-6-5-7] tetracyclic core of Calyciphylline ...
Abstract: A suitably functionalized tricyclic adduct containing the common A,B,E rings found in caly...
This thesis details the studies towards the total synthesis of the calyciphylline A-type Daphniphyll...
Herein we describe synthetic efforts toward the total synthesis of calyciphylline B-type alkaloids. ...
The dissertation herein describes the first total synthesis of the complex Daphniphyllum alkaloid, (...
We provide a full account of our synthetic studies targeting the hexacyclic calyciphylline B-type al...
The Daphniphyllum alkaloids are a diverse family of natural products rich in number and structural d...
The first total synthesis of the complex hexacylic Daphniphyllum alkaloid (–)-daphlongamine H in ena...
The first total synthesis of the complex hexacylic Daphniphyllum alkaloid (−)-daphlongamine H has be...
We will elaborate in this talk a stereochemically controlled route to the enantio-pure[6-6-5-7]tetra...
Herein, we report the enantioselective synthesis of a functionalized aza-octahydropentalene and its ...
The total synthesis of the architecturally complex <i>Daphniphyllum</i> alkaloid (−)-calyciphyllin...
Presented here is a full account on the development of a strategy culminating in the first total syn...
A stereochemically controlled route to the enantiopure [6–6–5–7] tetracyclic core of <i>Calyciphylli...
The dissertation herein describes the first total synthesis of the complex Daphniphyllum alkaloid, (...
A stereochemically controlled route to the enantiopure [6-6-5-7] tetracyclic core of Calyciphylline ...
Abstract: A suitably functionalized tricyclic adduct containing the common A,B,E rings found in caly...
This thesis details the studies towards the total synthesis of the calyciphylline A-type Daphniphyll...
Herein we describe synthetic efforts toward the total synthesis of calyciphylline B-type alkaloids. ...
The dissertation herein describes the first total synthesis of the complex Daphniphyllum alkaloid, (...
We provide a full account of our synthetic studies targeting the hexacyclic calyciphylline B-type al...
The Daphniphyllum alkaloids are a diverse family of natural products rich in number and structural d...
The first total synthesis of the complex hexacylic Daphniphyllum alkaloid (–)-daphlongamine H in ena...
The first total synthesis of the complex hexacylic Daphniphyllum alkaloid (−)-daphlongamine H has be...
We will elaborate in this talk a stereochemically controlled route to the enantio-pure[6-6-5-7]tetra...
Herein, we report the enantioselective synthesis of a functionalized aza-octahydropentalene and its ...
The total synthesis of the architecturally complex <i>Daphniphyllum</i> alkaloid (−)-calyciphyllin...
Presented here is a full account on the development of a strategy culminating in the first total syn...
A stereochemically controlled route to the enantiopure [6–6–5–7] tetracyclic core of <i>Calyciphylli...
The dissertation herein describes the first total synthesis of the complex Daphniphyllum alkaloid, (...
A stereochemically controlled route to the enantiopure [6-6-5-7] tetracyclic core of Calyciphylline ...
Abstract: A suitably functionalized tricyclic adduct containing the common A,B,E rings found in caly...
This thesis details the studies towards the total synthesis of the calyciphylline A-type Daphniphyll...