A Chemistry Cascade: From Physical Organic Studies of Alkoxy Radicals to Alkaloid Synthesis

In this Perspective, I present a personal account of a succession of chemical projects that I was involved with, each of which triggered or initiated my next research undertaking. It started with my early work in the field of physical organic photochemistry, which, in turn, guided me to my current r...

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Published inJournal of organic chemistry Vol. 74; no. 17; pp. 6421 - 6441
Main Author Padwa, Albert
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 04.09.2009
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Online AccessGet full text
ISSN0022-3263
1520-6904
1520-6904
DOI10.1021/jo901300x

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Abstract In this Perspective, I present a personal account of a succession of chemical projects that I was involved with, each of which triggered or initiated my next research undertaking. It started with my early work in the field of physical organic photochemistry, which, in turn, guided me to my current research dealing with the synthesis of biologically active alkaloids. The article highlights some of the dominant themes of my research program over the past 48 years. Subject matter that is discussed includes the generation of reactive intermediates by photoexcitation, [1,3]-dipolar cycloaddition chemistry, rhodium(II)-catalyzed domino reactions of α-diazo carbonyl compounds, intramolecular [4 + 2]-cycloaddition of 2-amidofurans, and the utilization of various thio fragments for the synthesis of nitrogen heterocycles.
AbstractList In this Perspective, I present a personal account of a succession of chemical projects that I was involved with, each of which triggered or initiated my next research undertaking. It started with my early work in the field of physical organic photochemistry, which, in turn, guided me to my current research dealing with the synthesis of biologically active alkaloids. The article highlights some of the dominant themes of my research program over the past 48 years. Subject matter that is discussed includes the generation of reactive intermediates by photoexcitation, [1,3]-dipolar cycloaddition chemistry, rhodium(II)-catalyzed domino reactions of alpha-diazo carbonyl compounds, intramolecular [4 + 2]-cycloaddition of 2-amidofurans, and the utilization of various thio fragments for the synthesis of nitrogen heterocycles.
In this Perspective, I present a personal account of a succession of chemical projects that I was involved with, each of which triggered or initiated my next research undertaking. It started with my early work in the field of physical organic photochemistry, which, in turn, guided me to my current research dealing with the synthesis of biologically active alkaloids. The article highlights some of the dominant themes of my research program over the past 48 years. Subject matter that is discussed includes the generation of reactive intermediates by photoexcitation, [1,3]-dipolar cycloaddition chemistry, rhodium(II)-catalyzed domino reactions of α-diazo carbonyl compounds, intramolecular [4 + 2]-cycloaddition of 2-amidofurans, and the utilization of various thio fragments for the synthesis of nitrogen heterocycles.
In this Perspective, I present a personal account of a succession of chemical projects that I was involved with, each of which triggered or initiated my next research undertaking. It started with my early work in the field of physical organic photochemistry, which, in turn, guided me to my current research dealing with the synthesis of biologically active alkaloids. The article highlights some of the dominant themes of my research program over the past 48 years. Subject matter that is discussed includes the generation of reactive intermediates by photoexcitation, [1,3]-dipolar cycloaddition chemistry, rhodium(II)-catalyzed domino reactions of alpha-diazo carbonyl compounds, intramolecular [4 + 2]-cycloaddition of 2-amidofurans, and the utilization of various thio fragments for the synthesis of nitrogen heterocycles.In this Perspective, I present a personal account of a succession of chemical projects that I was involved with, each of which triggered or initiated my next research undertaking. It started with my early work in the field of physical organic photochemistry, which, in turn, guided me to my current research dealing with the synthesis of biologically active alkaloids. The article highlights some of the dominant themes of my research program over the past 48 years. Subject matter that is discussed includes the generation of reactive intermediates by photoexcitation, [1,3]-dipolar cycloaddition chemistry, rhodium(II)-catalyzed domino reactions of alpha-diazo carbonyl compounds, intramolecular [4 + 2]-cycloaddition of 2-amidofurans, and the utilization of various thio fragments for the synthesis of nitrogen heterocycles.
Author Padwa, Albert
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Issue 17
Keywords Reaction intermediate
Intramolecular reaction
1,3-Dipolar cycloaddition
Catalytic reaction
Alkoxyl
Nitrogen heterocycle
Furan derivatives
Oxygen heterocycle
Biological activity
Organic sulfide
Alkaloid
Carbonyl Compounds
Diazo compound
Chemical synthesis
Rhodium II
Photochemistry
Photoexcitation
Successive reaction
Language English
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RelatedPersons Albert A Padwa
Padwa Albert
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Snippet In this Perspective, I present a personal account of a succession of chemical projects that I was involved with, each of which triggered or initiated my next...
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SubjectTerms Alkaloids - chemical synthesis
Alkaloids - chemistry
Animals
Chemistry
Chemistry, Organic - history
Chemistry, Organic - methods
Coleoptera
Exact sciences and technology
Female
Furans - chemistry
General and physical chemistry
Heterocyclic compounds
History, 20th Century
History, 21st Century
Kinetics and mechanisms
Molecular Structure
Nitrogen - chemistry
Organic chemistry
Padwa Albert
Photochemistry
Photochemistry - methods
Physical chemistry of induced reactions (with radiations, particles and ultrasonics)
Preparations and properties
Reactivity and mechanisms
Title A Chemistry Cascade: From Physical Organic Studies of Alkoxy Radicals to Alkaloid Synthesis
URI http://dx.doi.org/10.1021/jo901300x
https://www.ncbi.nlm.nih.gov/pubmed/19663447
https://www.proquest.com/docview/734018479
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