A versatile chiron approach to the tetrahydropyranyl diarylheptanoid natural products (−)-centrolobine and (+)-centrolobine has been described. The use of an aldol reaction followed by reductive etherification for the formation of tetrahydropyran ring is of importance
A new tetrahydropyranone synthesis has been developed that leads to cis-2,6-disubstituted 3,3-dimeth...
A highly stereoselective route to 2,4,5-trisubstituted tetrahydropyrans is reported. The key step em...
A diastereoselective synthesis of <i>cis</i>-2,6-disubstituted tetrahydropyran-4-ones was developed....
A chiron approach for the total synthesis of (+)-centrolobine has been described from the commercial...
Stereoselective formal synthesis of (-)-centrolobine was achieved from naturally occurring L-(+)-tar...
A highly stereoselective construction of 2,6-<i>cis</i>-disubstituted tetrahydropyrans was achieved ...
The reaction of aldehydes with homoallyl alcohols in the presence of TMSI generated in situ from TMS...
A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and o...
A short, formal stereoselective synthesis of the naturally occurring tetrahydropyran derivative ophi...
The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported...
Dihydropyrans are important structural motifs that are found within many natural products and biolog...
6-Substituted-2H-dihydropyran-4-one products of the Maitland-Japp reaction have been converted into ...
ABSTRACT: A diastereoselective synthesis of cis-2,6-disubstituted tetrahydropyran-4-ones was develop...
cis-2,6-Tetrahydropyran is an important structural skeleton of bioactive natural products. A facile ...
A diastereoselective synthesis of cis-2,6-disubstituted tetrahydropyran-4-ones was developed. The ke...
A new tetrahydropyranone synthesis has been developed that leads to cis-2,6-disubstituted 3,3-dimeth...
A highly stereoselective route to 2,4,5-trisubstituted tetrahydropyrans is reported. The key step em...
A diastereoselective synthesis of <i>cis</i>-2,6-disubstituted tetrahydropyran-4-ones was developed....
A chiron approach for the total synthesis of (+)-centrolobine has been described from the commercial...
Stereoselective formal synthesis of (-)-centrolobine was achieved from naturally occurring L-(+)-tar...
A highly stereoselective construction of 2,6-<i>cis</i>-disubstituted tetrahydropyrans was achieved ...
The reaction of aldehydes with homoallyl alcohols in the presence of TMSI generated in situ from TMS...
A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and o...
A short, formal stereoselective synthesis of the naturally occurring tetrahydropyran derivative ophi...
The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported...
Dihydropyrans are important structural motifs that are found within many natural products and biolog...
6-Substituted-2H-dihydropyran-4-one products of the Maitland-Japp reaction have been converted into ...
ABSTRACT: A diastereoselective synthesis of cis-2,6-disubstituted tetrahydropyran-4-ones was develop...
cis-2,6-Tetrahydropyran is an important structural skeleton of bioactive natural products. A facile ...
A diastereoselective synthesis of cis-2,6-disubstituted tetrahydropyran-4-ones was developed. The ke...
A new tetrahydropyranone synthesis has been developed that leads to cis-2,6-disubstituted 3,3-dimeth...
A highly stereoselective route to 2,4,5-trisubstituted tetrahydropyrans is reported. The key step em...
A diastereoselective synthesis of <i>cis</i>-2,6-disubstituted tetrahydropyran-4-ones was developed....
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