Semi-syntheses and interrogation of indole-substituted Aspidosperma terpenoid alkaloids. Read more about Semi-syntheses and interrogation of indole-substituted Aspidosperma terpenoid alkaloids.
Differential scanning fluorimetry (DSF) screen to identify inhibitors of Hsp60 protein-protein interactions. Read more about Differential scanning fluorimetry (DSF) screen to identify inhibitors of Hsp60 protein-protein interactions.
A threonine turnstile defines a dynamic amphiphilic binding motif in the AAA ATPase p97 allosteric binding site. Read more about A threonine turnstile defines a dynamic amphiphilic binding motif in the AAA ATPase p97 allosteric binding site.
Towards aspirin-inspired self-immolating molecules which target the cyclooxygenases. Read more about Towards aspirin-inspired self-immolating molecules which target the cyclooxygenases.
Replication of biosynthetic reactions enables efficient synthesis of A-factor, a γ-butyrolactone autoinducer from Streptomyces griseus. Read more about Replication of biosynthetic reactions enables efficient synthesis of A-factor, a γ-butyrolactone autoinducer from Streptomyces griseus.
Efficient conversion of triacylglycerols and fatty acids to biodiesel in a microwave reactor using metal triflate catalysts. Read more about Efficient conversion of triacylglycerols and fatty acids to biodiesel in a microwave reactor using metal triflate catalysts.
Bypassing stereoselectivity in the early steps of alkaloid biosynthesis. Read more about Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.
Synthesis and pharmacological effects of the enantiomers of the N-phenethyl analogues of the ortho and para e- and f-oxide-bridged phenylmorphans. Read more about Synthesis and pharmacological effects of the enantiomers of the N-phenethyl analogues of the ortho and para e- and f-oxide-bridged phenylmorphans.
Glutathione traps formaldehyde by formation of a bicyclo[4.4.1]undecane adduct. Read more about Glutathione traps formaldehyde by formation of a bicyclo[4.4.1]undecane adduct.
Formation of an aminoacyl-S-enzyme intermediate is a key step in the biosynthesis of chloramphenicol. Read more about Formation of an aminoacyl-S-enzyme intermediate is a key step in the biosynthesis of chloramphenicol.
