The total synthesis of (+)-crocacin C is described. The convergent asymmetric synthesis relies on the use of a regio- and diastereoselective epoxidation of an allylic alcohol with m-CPBA followed by epoxide opening with Me2CuCNLi2 and a Stille cross-coupling between E-vinyl stannane 5 and E-vinyl iodide 6 to establish the (E,E)-dienamide moiety
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
The total synthesis of (+)-crocacin C is described. The convergent asymmetric synthesis relies on th...
The total synthesis of (+)-crocacin D is described. The convergent asymmetric synthesis relies on th...
The total synthesis of (+)-crocacin D is described. The convergent asymmetric synthesis relies on th...
[structure: see text] The total synthesis of (+)-crocacin D is described. The convergent asymmetric ...
The total synthesis of potent antifungal and cytotoxic agent (+)-crocacin C in optically pure form f...
The first total synthesis of the potent antifungal and cytotoxic agent (+)-crocacin D in optically p...
The first total synthesis of the potent antifungal and cytotoxic agent (+)-crocacin D in optically p...
Total synthesis of the potent antifungal and cytotoxic agent (+)-crocacin A is described. The crucia...
An efficient total synthesis of a potent antifungal and moderate cytotoxic agent crocacin C is descr...
O capítulo 1 relata as sínteses totais assimétricas das (+)-crocacinas C (1.3) e D (1.4). A síntese ...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
The total synthesis of (+)-crocacin C is described. The convergent asymmetric synthesis relies on th...
The total synthesis of (+)-crocacin D is described. The convergent asymmetric synthesis relies on th...
The total synthesis of (+)-crocacin D is described. The convergent asymmetric synthesis relies on th...
[structure: see text] The total synthesis of (+)-crocacin D is described. The convergent asymmetric ...
The total synthesis of potent antifungal and cytotoxic agent (+)-crocacin C in optically pure form f...
The first total synthesis of the potent antifungal and cytotoxic agent (+)-crocacin D in optically p...
The first total synthesis of the potent antifungal and cytotoxic agent (+)-crocacin D in optically p...
Total synthesis of the potent antifungal and cytotoxic agent (+)-crocacin A is described. The crucia...
An efficient total synthesis of a potent antifungal and moderate cytotoxic agent crocacin C is descr...
O capítulo 1 relata as sínteses totais assimétricas das (+)-crocacinas C (1.3) e D (1.4). A síntese ...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
International audienceA highly convergent and protecting-group-free synthesis of (+)-crocacin C, fea...
A formal synthesis of crocacin C is described proving the versatility of Prins cyclization in natura...
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