Chapter 1. Recent synthetic approaches towards the resveratrol family of oligomeric natural Products This chapter outlines some of the past and present efforts in the field of resveratrol-based oligomeric natural product synthesis. Both biosynthetic approaches and stepwise synthetic approaches are discussed to present the current level of understanding regarding the controlled synthesis of these molecules in order to place the studies described in chapter 2 and 3 in better context. Chapter 2. Development of a general synthetic method towards different dimeric structures of the resveratrol family We have developed a general approach to achieve selective synthesis of the major dimeric architectures within the resveratrol family with the use o...
A resume of four lectures presented by the author during a one month visit to BIOTROPÂ...
Fig. 15. Chemical synthesis of resveratrol derivatives: The derivatives 3,4′,5-trimethoxy-cis-stilbe...
The resveratrol analogues have attracted great attension by scientists as these compounds exhibit nu...
Chapter 1. Recent synthetic approaches towards the resveratrol family of oligomeric natural products...
The family of oligomeric natural products derived from resveratrol possesses broad pharmacological p...
Numerous reports exist for the biological properties of resveratrol natural products and many clinic...
PART I Controllable Synthesis of Complex Members of the Resveratrol Oligomer Family Chap...
Numerous reports of therapeutically relevant biological activities of resveratrol (3,4ʹ,5-trihydroxy...
Research interest in resveratrol, a structurally simple plant metabolite, has increased exponentiall...
Although much attention has been devoted to resveratrol, a unique polyphenol produced by plants thro...
Since their discovery 120 years ago, carbon-centered free radicals have captivated the attention of ...
The chemo-enzymatic synthesis and the evaluation of radical scavenger performance of resveratrolrela...
Biotransformation of trans-resveratrol and synthetic (±)-ε-viniferin in aqueous acetone using horser...
Resveratrol oligomers (REVs), a major class of stilbenoids, are biosynthesized by regioselective oxi...
A resume of four lectures presented by the author during a one month visit to BIOTROP in 199...
A resume of four lectures presented by the author during a one month visit to BIOTROPÂ...
Fig. 15. Chemical synthesis of resveratrol derivatives: The derivatives 3,4′,5-trimethoxy-cis-stilbe...
The resveratrol analogues have attracted great attension by scientists as these compounds exhibit nu...
Chapter 1. Recent synthetic approaches towards the resveratrol family of oligomeric natural products...
The family of oligomeric natural products derived from resveratrol possesses broad pharmacological p...
Numerous reports exist for the biological properties of resveratrol natural products and many clinic...
PART I Controllable Synthesis of Complex Members of the Resveratrol Oligomer Family Chap...
Numerous reports of therapeutically relevant biological activities of resveratrol (3,4ʹ,5-trihydroxy...
Research interest in resveratrol, a structurally simple plant metabolite, has increased exponentiall...
Although much attention has been devoted to resveratrol, a unique polyphenol produced by plants thro...
Since their discovery 120 years ago, carbon-centered free radicals have captivated the attention of ...
The chemo-enzymatic synthesis and the evaluation of radical scavenger performance of resveratrolrela...
Biotransformation of trans-resveratrol and synthetic (±)-ε-viniferin in aqueous acetone using horser...
Resveratrol oligomers (REVs), a major class of stilbenoids, are biosynthesized by regioselective oxi...
A resume of four lectures presented by the author during a one month visit to BIOTROP in 199...
A resume of four lectures presented by the author during a one month visit to BIOTROPÂ...
Fig. 15. Chemical synthesis of resveratrol derivatives: The derivatives 3,4′,5-trimethoxy-cis-stilbe...
The resveratrol analogues have attracted great attension by scientists as these compounds exhibit nu...