A versatile three-step, one-pot, sequential reaction protocol involving RCM, CM, and chemoselective hydrogenation is reported. This phosphate tether-mediated process occurs without intermediate isolation, is chemoselective and is governed by stereoelectronic properties innate to phosphate tethers, which ultimately act to preserve the integrity of the bisallylic, bicyclic phosphate for subsequent nucleophilic additions. Overall, this process can be used to efficiently generate advanced polyol synthons
This is the peer reviewed version of the following article: Chegondi, R., Maitra, S., Markley, J. L....
The development of atom-, redox-, step-, and pot-economical methods for the efficient synthesis of m...
AbstractA one-pot procedure for the phosphorylation of alcohols provides the corresponding phosphate...
A versatile three-step, one-pot, sequential reaction protocol involving RCM, CM, and chemoselective ...
A versatile three-step, one-pot, sequential reaction protocol involving ring-closing metathesis, cro...
This investigation was generously supported by funds provided by the National Institute of General M...
Over the past decade, work in our lab has focused on phosphate tether-mediated desymmetrization of C...
The development of atom-, redox-, and step-, and pot-economonical strategies for the streamlined syn...
Dissertation (Ph.D.)--University of Kansas, Chemistry, 2007.The use of phosphate esters as temporary...
This is the peer reviewed version of the following article: Thomas, C. D., McParland, J. P. and Hans...
The focus of this dissertation is the desymmetrization of C2-symmetric 1,3-anti-diols through the co...
An efficient synthesis of (−)-tetrahydrolipstatin (THL) is reported. This method takes advantage of ...
The utilization of phosphate tethers in synthesis is the focus of the dissertation research describe...
A phosphate tether-mediated ring-closing metathesis study towards the synthesis of P-stereogenic bic...
The focus of this dissertation is the utilization of phosphate tether mediated approaches to synthes...
This is the peer reviewed version of the following article: Chegondi, R., Maitra, S., Markley, J. L....
The development of atom-, redox-, step-, and pot-economical methods for the efficient synthesis of m...
AbstractA one-pot procedure for the phosphorylation of alcohols provides the corresponding phosphate...
A versatile three-step, one-pot, sequential reaction protocol involving RCM, CM, and chemoselective ...
A versatile three-step, one-pot, sequential reaction protocol involving ring-closing metathesis, cro...
This investigation was generously supported by funds provided by the National Institute of General M...
Over the past decade, work in our lab has focused on phosphate tether-mediated desymmetrization of C...
The development of atom-, redox-, and step-, and pot-economonical strategies for the streamlined syn...
Dissertation (Ph.D.)--University of Kansas, Chemistry, 2007.The use of phosphate esters as temporary...
This is the peer reviewed version of the following article: Thomas, C. D., McParland, J. P. and Hans...
The focus of this dissertation is the desymmetrization of C2-symmetric 1,3-anti-diols through the co...
An efficient synthesis of (−)-tetrahydrolipstatin (THL) is reported. This method takes advantage of ...
The utilization of phosphate tethers in synthesis is the focus of the dissertation research describe...
A phosphate tether-mediated ring-closing metathesis study towards the synthesis of P-stereogenic bic...
The focus of this dissertation is the utilization of phosphate tether mediated approaches to synthes...
This is the peer reviewed version of the following article: Chegondi, R., Maitra, S., Markley, J. L....
The development of atom-, redox-, step-, and pot-economical methods for the efficient synthesis of m...
AbstractA one-pot procedure for the phosphorylation of alcohols provides the corresponding phosphate...