In this thesis, methodology developments for the synthesis of cyclic imines employing a series of alkene aminofunctionalizations will be described. These methods involve the utilization of imine derivatives such as N−H ketimines and amidines as nitrogen precursors for haloamination as well as aminooxygenation of alkenes.Doctor of Philosophy (SPMS
Thesis (Ph.D.)--University of Washington, 2012A plethora of natural products and valuable pharmaceut...
This dissertation describes studies on carbo- and amino-functionalization of alkenes using conjugate...
This thesis consists of four chapters. In chapter 1, a brief overview about the difunctionalization ...
The application of [4+2] cycloadditions between alkenes and an N-benzoyl iminium species, generated ...
Nitrogen-containing heterocyclic compounds are very important to the pharmaceutical and agrochemical...
Complex cyclic azomethine imines possessing a β-aminocarbonyl motif can be accessed readily from sim...
This thesis focused on the development of transition metal-free amino-cyclization towards the synthe...
The functionalization of non-activated C–H bond of cyclic amines is of great importance due to the u...
Functionalization of amines is a very important research area in organic chemistry because functiona...
The α-functionalization of amines is a synthetic challenge of much interest to organic chemists. Com...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
CNRS T Bordereau / INIST-CNRS - Institut de l'Information Scientifique et TechniqueSIGLEFRFranc
The aminocarbonylation of alkenes is a powerful method for accessing the β-amino carbonyl motif that...
The aminocarbonylation of alkenes is a powerful method for accessing the β-amino carbonyl motif that...
This dissertation describes studies on carbo- and amino-functionalization of alkenes using conjugate...
Thesis (Ph.D.)--University of Washington, 2012A plethora of natural products and valuable pharmaceut...
This dissertation describes studies on carbo- and amino-functionalization of alkenes using conjugate...
This thesis consists of four chapters. In chapter 1, a brief overview about the difunctionalization ...
The application of [4+2] cycloadditions between alkenes and an N-benzoyl iminium species, generated ...
Nitrogen-containing heterocyclic compounds are very important to the pharmaceutical and agrochemical...
Complex cyclic azomethine imines possessing a β-aminocarbonyl motif can be accessed readily from sim...
This thesis focused on the development of transition metal-free amino-cyclization towards the synthe...
The functionalization of non-activated C–H bond of cyclic amines is of great importance due to the u...
Functionalization of amines is a very important research area in organic chemistry because functiona...
The α-functionalization of amines is a synthetic challenge of much interest to organic chemists. Com...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
CNRS T Bordereau / INIST-CNRS - Institut de l'Information Scientifique et TechniqueSIGLEFRFranc
The aminocarbonylation of alkenes is a powerful method for accessing the β-amino carbonyl motif that...
The aminocarbonylation of alkenes is a powerful method for accessing the β-amino carbonyl motif that...
This dissertation describes studies on carbo- and amino-functionalization of alkenes using conjugate...
Thesis (Ph.D.)--University of Washington, 2012A plethora of natural products and valuable pharmaceut...
This dissertation describes studies on carbo- and amino-functionalization of alkenes using conjugate...
This thesis consists of four chapters. In chapter 1, a brief overview about the difunctionalization ...