A convergent strategy for the synthesis of dideoxysalarin C (3) as a potential intermediate for the total synthesis of the marine macrolide salarin C (1) is described. The macrolactone core of 3 was assembled by Suzuki coupling between alkyl iodide 9 and vinyl iodide 8 and Shiina macrolactonization as key transformations. All macrocyclic intermediates were found to be of low stability
A stereocontrolled total synthesis of the microfilament-destabilizing cytotoxic macrolide (−)-reidis...
Concise, flexible and high yielding approaches to the orsellinic acid type macrolides lasiodiplodin ...
The chemical modification of structurally complex fermentation products, a process known as semisynt...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN017473 / BLDSC - British Library D...
The synthesis of the macrocyclic core of the cytotoxic natural product salarin C from the sponge Fas...
Die Salarine A–J aus dem Meeresschwamm Fascaplysinopsis sp. bilden eine einzigartige Familie von 17-...
The stereoselective total synthesis of cytotoxic marine macrolide callyspongiolide has been reported...
Marvel of the sea: A concise and highly convergent total synthesis of the methyl ester of the marine...
Organometallic chemistry in general and catalysis in particular are used in the first total synthesi...
The increasing resistance to antibiotics is becoming a major threat to public health. An increasing ...
Macrocyclic scaffolds are commonly found in bioactive natural products and pharmaceutical molecules....
The first total synthesis of achaetolide, a 10-membered macrolactone was achieved using Mitsunobu re...
The synthesis of an appropriately functionalized advanced C(6–28) fragment (<b>3</b>) of the marine ...
International audienceA new and efficient convergent approach toward the synthesis of amphidinolide ...
An efficient synthesis of the macrolactone 3 of the salicylihalamides in 10 linear steps from alkene...
A stereocontrolled total synthesis of the microfilament-destabilizing cytotoxic macrolide (−)-reidis...
Concise, flexible and high yielding approaches to the orsellinic acid type macrolides lasiodiplodin ...
The chemical modification of structurally complex fermentation products, a process known as semisynt...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN017473 / BLDSC - British Library D...
The synthesis of the macrocyclic core of the cytotoxic natural product salarin C from the sponge Fas...
Die Salarine A–J aus dem Meeresschwamm Fascaplysinopsis sp. bilden eine einzigartige Familie von 17-...
The stereoselective total synthesis of cytotoxic marine macrolide callyspongiolide has been reported...
Marvel of the sea: A concise and highly convergent total synthesis of the methyl ester of the marine...
Organometallic chemistry in general and catalysis in particular are used in the first total synthesi...
The increasing resistance to antibiotics is becoming a major threat to public health. An increasing ...
Macrocyclic scaffolds are commonly found in bioactive natural products and pharmaceutical molecules....
The first total synthesis of achaetolide, a 10-membered macrolactone was achieved using Mitsunobu re...
The synthesis of an appropriately functionalized advanced C(6–28) fragment (<b>3</b>) of the marine ...
International audienceA new and efficient convergent approach toward the synthesis of amphidinolide ...
An efficient synthesis of the macrolactone 3 of the salicylihalamides in 10 linear steps from alkene...
A stereocontrolled total synthesis of the microfilament-destabilizing cytotoxic macrolide (−)-reidis...
Concise, flexible and high yielding approaches to the orsellinic acid type macrolides lasiodiplodin ...
The chemical modification of structurally complex fermentation products, a process known as semisynt...