The Experts below are selected from a list of 21 Experts worldwide ranked by ideXlab platform
Alessandra Silvani - One of the best experts on this subject based on the ideXlab platform.
-
stereocontrolled reduction of an oxazepinohexahydroindolo 2 3 a Quinolizine Derivative asymmetric total synthesis of tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
'Elsevier BV', 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Efficient, stereocontrolled total synthesis of the title compound is described. starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative. (C) 2001 Elsevier Science Ltd. All rights reserved
Bruno Danieli - One of the best experts on this subject based on the ideXlab platform.
-
stereocontrolled reduction of an oxazepinohexahydroindolo 2 3 a Quinolizine Derivative asymmetric total synthesis of tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
'Elsevier BV', 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Efficient, stereocontrolled total synthesis of the title compound is described. starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative. (C) 2001 Elsevier Science Ltd. All rights reserved
Giordano Lesma - One of the best experts on this subject based on the ideXlab platform.
-
stereocontrolled reduction of an oxazepinohexahydroindolo 2 3 a Quinolizine Derivative asymmetric total synthesis of tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
'Elsevier BV', 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Efficient, stereocontrolled total synthesis of the title compound is described. starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative. (C) 2001 Elsevier Science Ltd. All rights reserved
Daniele Passarella - One of the best experts on this subject based on the ideXlab platform.
-
stereocontrolled reduction of an oxazepinohexahydroindolo 2 3 a Quinolizine Derivative asymmetric total synthesis of tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
'Elsevier BV', 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Efficient, stereocontrolled total synthesis of the title compound is described. starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative. (C) 2001 Elsevier Science Ltd. All rights reserved
Alessandro Sacchetti - One of the best experts on this subject based on the ideXlab platform.
-
stereocontrolled reduction of an oxazepinohexahydroindolo 2 3 a Quinolizine Derivative asymmetric total synthesis of tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
Tetrahedron Letters, 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Abstract Efficient, stereocontrolled total synthesis of the title compound is described, starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3- a ]Quinolizine Derivative.
-
Stereocontrolled reduction of an oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative: asymmetric total synthesis of (+)-tacamonine
'Elsevier BV', 2001Co-Authors: Bruno Danieli, Giordano Lesma, Daniele Passarella, Alessandro Sacchetti, Alessandra SilvaniAbstract:Efficient, stereocontrolled total synthesis of the title compound is described. starting from enantiopure intermediates. A key step was the diastereoselective catalytic hydrogenation of a pentacyclic oxazepinohexahydroindolo[2,3-a]Quinolizine Derivative. (C) 2001 Elsevier Science Ltd. All rights reserved
