The total synthesis of biselide E, a marine polyketide isolated from the Okinawan ascidian, has been accomplished. The highlight of this approach is the use of the β-elimination reaction of the chloroacetoxy group for the construction of an unstable six-membered α,β,γ,δ-unsaturated lactone portion at the late stage of the total synthesis
An enantioselective approach toward the recently isolated marine natural product, spiculoic acid A, ...
An enantioselective approach toward the recently isolated marine natural product, spiculoic acid A, ...
The total synthesis of the polyketide antibiotic (-)-basiliskamide B is described. The convergent as...
Modern pharmaceuticals originate predominately either from natural products or totally synthetic com...
The use of natural products for medicinal purposes is a tradition dating back to ancient times. To t...
The primary focus of the research described in this thesis deals with the studies geared towards the...
After the isolation of the bioactive polyether bistramide C from the marine ascidian Lissoclinum bis...
Recently, some bisabolene derivatives were isolated from the marine sponge Myrmekioderma sp. These d...
We wish to describe here our continuing efforts towards the total synthesis of the marine sponge pol...
The synthesis of Arctic sponge alkaloid viscosaline (1) is achieved by using the Zincke reaction as ...
The research contained herein describes the use of organic synthesis to answer fundamental questions...
4-Amino-7-(5′-deoxy-β-d-xylofuranosyl)-5-iodo-pyrrolo[2,3-d]pyrimidine 1, an unusual naturally occur...
The first part of this dissertation describes the revised stereochemical assignment of the cytotoxic...
This dissertation describes the development and partial execution of a unified synthetic strategy fo...
The bistramides are a class of natural products isolated from the marine ascidian Lissoclinum bistra...
An enantioselective approach toward the recently isolated marine natural product, spiculoic acid A, ...
An enantioselective approach toward the recently isolated marine natural product, spiculoic acid A, ...
The total synthesis of the polyketide antibiotic (-)-basiliskamide B is described. The convergent as...
Modern pharmaceuticals originate predominately either from natural products or totally synthetic com...
The use of natural products for medicinal purposes is a tradition dating back to ancient times. To t...
The primary focus of the research described in this thesis deals with the studies geared towards the...
After the isolation of the bioactive polyether bistramide C from the marine ascidian Lissoclinum bis...
Recently, some bisabolene derivatives were isolated from the marine sponge Myrmekioderma sp. These d...
We wish to describe here our continuing efforts towards the total synthesis of the marine sponge pol...
The synthesis of Arctic sponge alkaloid viscosaline (1) is achieved by using the Zincke reaction as ...
The research contained herein describes the use of organic synthesis to answer fundamental questions...
4-Amino-7-(5′-deoxy-β-d-xylofuranosyl)-5-iodo-pyrrolo[2,3-d]pyrimidine 1, an unusual naturally occur...
The first part of this dissertation describes the revised stereochemical assignment of the cytotoxic...
This dissertation describes the development and partial execution of a unified synthetic strategy fo...
The bistramides are a class of natural products isolated from the marine ascidian Lissoclinum bistra...
An enantioselective approach toward the recently isolated marine natural product, spiculoic acid A, ...
An enantioselective approach toward the recently isolated marine natural product, spiculoic acid A, ...
The total synthesis of the polyketide antibiotic (-)-basiliskamide B is described. The convergent as...