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Arundo Donax
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Christopher M. Beaudry – One of the best experts on this subject based on the ideXlab platform.
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synthesis of bis indole alkaloids from Arundo Donax the ynindole diels alder reaction conformational chirality and absolute stereochemistry
ChemInform, 2015Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:The synthesis of Arundo Donax alkaloids such as (III) is developed based on the first Diels—Alder reaction of the ynindole functional group.
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Synthesis of Bis(indole) Alkaloids from Arundo Donax: The Ynindole Diels—Alder Reaction, Conformational Chirality, and Absolute Stereochemistry.
ChemInform, 2015Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:The synthesis of Arundo Donax alkaloids such as (III) is developed based on the first Diels—Alder reaction of the ynindole functional group.
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Synthesis of bis(indole) alkaloids from Arundo Donax: the ynindole Diels-Alder reaction, conformational chirality, and absolute stereochemistry.
Angewandte Chemie, 2014Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:Bis(indole) alkaloids from Arundo Donax were synthesized using the first ynindole Diels–Alder reaction. The alkaloids are chiral, having stable enantiomeric conformations with half-lives of racemization of t1/2=4150–25100 seconds at room temperature. Their absolute stereochemistry was determined using the exciton chirality method.
Jingjin Chen – One of the best experts on this subject based on the ideXlab platform.
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synthesis of bis indole alkaloids from Arundo Donax the ynindole diels alder reaction conformational chirality and absolute stereochemistry
ChemInform, 2015Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:The synthesis of Arundo Donax alkaloids such as (III) is developed based on the first Diels—Alder reaction of the ynindole functional group.
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Synthesis of Bis(indole) Alkaloids from Arundo Donax: The Ynindole Diels—Alder Reaction, Conformational Chirality, and Absolute Stereochemistry.
ChemInform, 2015Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:The synthesis of Arundo Donax alkaloids such as (III) is developed based on the first Diels—Alder reaction of the ynindole functional group.
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Synthesis of bis(indole) alkaloids from Arundo Donax: the ynindole Diels-Alder reaction, conformational chirality, and absolute stereochemistry.
Angewandte Chemie, 2014Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:Bis(indole) alkaloids from Arundo Donax were synthesized using the first ynindole Diels–Alder reaction. The alkaloids are chiral, having stable enantiomeric conformations with half-lives of racemization of t1/2=4150–25100 seconds at room temperature. Their absolute stereochemistry was determined using the exciton chirality method.
Andrew J. Ferreira – One of the best experts on this subject based on the ideXlab platform.
-
synthesis of bis indole alkaloids from Arundo Donax the ynindole diels alder reaction conformational chirality and absolute stereochemistry
ChemInform, 2015Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:The synthesis of Arundo Donax alkaloids such as (III) is developed based on the first Diels—Alder reaction of the ynindole functional group.
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Synthesis of Bis(indole) Alkaloids from Arundo Donax: The Ynindole Diels—Alder Reaction, Conformational Chirality, and Absolute Stereochemistry.
ChemInform, 2015Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:The synthesis of Arundo Donax alkaloids such as (III) is developed based on the first Diels—Alder reaction of the ynindole functional group.
-
Synthesis of bis(indole) alkaloids from Arundo Donax: the ynindole Diels-Alder reaction, conformational chirality, and absolute stereochemistry.
Angewandte Chemie, 2014Co-Authors: Jingjin Chen, Andrew J. Ferreira, Christopher M. BeaudryAbstract:Bis(indole) alkaloids from Arundo Donax were synthesized using the first ynindole Diels–Alder reaction. The alkaloids are chiral, having stable enantiomeric conformations with half-lives of racemization of t1/2=4150–25100 seconds at room temperature. Their absolute stereochemistry was determined using the exciton chirality method.