Add to ORKGThe total synthesis and structural revision of antibiotic CJ-16,264 is described. Starting with citronellal, the quest for the target molecule featured a novel bis-transannular Diels-Alder reaction that casted stereoselectively the decalin system and included the synthesis of six isomers before demystification of its true structure
Complete construction: The total synthesis of IKD-8344, a novel 28-membered ring macrodiolide antibi...
This thesis describes the first total synthesis of Thiocillin I, a thiopeptide antibiotic that is st...
The first total synthesis of the potent antibiotic disciformycin B (2) is described, which is except...
The total synthesis and structural revision of antibiotic CJ-16,264 is described. Starting with citr...
A study towards the natural product tetrodecamycin is reported. A modified Schlosser–Wittig reaction...
This thesis explores the development of the tandem oxy-Cope/ene rearrangement and its application to...
Decalin-containing natural products along with tetramic acid moieties present characteristic functio...
The total synthesis of the thiopeptide antibiotic, thiocillin I, is described. This work unequivocal...
9,10-Substituted cis and trans-decalins were synthesized by a simple route using the Diels-Alder rea...
Several recently accomplished total syntheses of antibiotic natural products were summarized in this...
A total asymmetric synthesis of the polyol subunit of the polyene macrolide antibiotic RK-397 was de...
This dissertation concerns the stereoselective synthesis of optically pure compound 196, the C₁₆-C₃₂...
A83586C isolated from the culture filtrates of Streptomyces Karnatakensis is a member of the Azinoth...
Since the discovery of the antibiotic penicillin, natural products-small mols. isolated from plants,...
The first total synthesis of thuggacin cmc-A and the determination of the absolute structure are des...
Complete construction: The total synthesis of IKD-8344, a novel 28-membered ring macrodiolide antibi...
This thesis describes the first total synthesis of Thiocillin I, a thiopeptide antibiotic that is st...
The first total synthesis of the potent antibiotic disciformycin B (2) is described, which is except...
The total synthesis and structural revision of antibiotic CJ-16,264 is described. Starting with citr...
A study towards the natural product tetrodecamycin is reported. A modified Schlosser–Wittig reaction...
This thesis explores the development of the tandem oxy-Cope/ene rearrangement and its application to...
Decalin-containing natural products along with tetramic acid moieties present characteristic functio...
The total synthesis of the thiopeptide antibiotic, thiocillin I, is described. This work unequivocal...
9,10-Substituted cis and trans-decalins were synthesized by a simple route using the Diels-Alder rea...
Several recently accomplished total syntheses of antibiotic natural products were summarized in this...
A total asymmetric synthesis of the polyol subunit of the polyene macrolide antibiotic RK-397 was de...
This dissertation concerns the stereoselective synthesis of optically pure compound 196, the C₁₆-C₃₂...
A83586C isolated from the culture filtrates of Streptomyces Karnatakensis is a member of the Azinoth...
Since the discovery of the antibiotic penicillin, natural products-small mols. isolated from plants,...
The first total synthesis of thuggacin cmc-A and the determination of the absolute structure are des...
Complete construction: The total synthesis of IKD-8344, a novel 28-membered ring macrodiolide antibi...
This thesis describes the first total synthesis of Thiocillin I, a thiopeptide antibiotic that is st...
The first total synthesis of the potent antibiotic disciformycin B (2) is described, which is except...