A chiron approach for the total synthesis of (+)-centrolobine has been described from the commercially available aldehyde 3 employing an acid-catalyzed stereoselective formation of tetrahydropyran ring as the key step. The desired molecule was accomplished in eight steps with 62% overall yield
A one-pot wonder: 1,2,3,4-Tetrahydroisoquinolines with a C4 stereocenter can be formed by using a on...
An efficient chiron approach to the total synthesis of (−)-tetrahydrolipstatin is described. The mai...
The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported...
A versatile chiron approach to the tetrahydropyranyl diarylheptanoid natural products (−)-centrolobi...
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 ...
A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and o...
The reaction of aldehydes with homoallyl alcohols in the presence of TMSI generated in situ from TMS...
An expedient total synthesis of (−)-centrolobine is achieved involving asymmetric Keck allylation an...
cis-2,6-Tetrahydropyran is an important structural skeleton of bioactive natural products. A facile ...
A flexible synthesis of the C1-C12 fragment of Tedanolide C has been accomplished in eight steps fro...
The goal of this study is the synthesis of centrolobine 7, a naturally-occuring compound that exhibi...
A flexible synthesis of the C1–C12 fragment of Tedanolide C has been accomplished in eight steps fro...
A new tetrahydropyranone synthesis has been developed that leads to cis-2,6-disubstituted 3,3-dimeth...
A catalytic asymmetric formal synthesis of diarylheptanoid natural product calyxin L has been achiev...
A one-pot wonder: 1,2,3,4-Tetrahydroisoquinolines with a C4 stereocenter can be formed by using a on...
An efficient chiron approach to the total synthesis of (−)-tetrahydrolipstatin is described. The mai...
The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported...
A versatile chiron approach to the tetrahydropyranyl diarylheptanoid natural products (−)-centrolobi...
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 ...
A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and o...
The reaction of aldehydes with homoallyl alcohols in the presence of TMSI generated in situ from TMS...
An expedient total synthesis of (−)-centrolobine is achieved involving asymmetric Keck allylation an...
cis-2,6-Tetrahydropyran is an important structural skeleton of bioactive natural products. A facile ...
A flexible synthesis of the C1-C12 fragment of Tedanolide C has been accomplished in eight steps fro...
The goal of this study is the synthesis of centrolobine 7, a naturally-occuring compound that exhibi...
A flexible synthesis of the C1–C12 fragment of Tedanolide C has been accomplished in eight steps fro...
A new tetrahydropyranone synthesis has been developed that leads to cis-2,6-disubstituted 3,3-dimeth...
A catalytic asymmetric formal synthesis of diarylheptanoid natural product calyxin L has been achiev...
A one-pot wonder: 1,2,3,4-Tetrahydroisoquinolines with a C4 stereocenter can be formed by using a on...
An efficient chiron approach to the total synthesis of (−)-tetrahydrolipstatin is described. The mai...
The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported...
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