The total synthesis of （±）-abyssinoflavanone V was first achieved through C-prenylation, selective protection of phenolic hydroxyl group, aldol condensation, cyclization and deprotection starting from cheap 4-h...The total synthesis of （±）-abyssinoflavanone V was first achieved through C-prenylation, selective protection of phenolic hydroxyl group, aldol condensation, cyclization and deprotection starting from cheap 4-hydroxybenzaldehyde and 2,4,6- trihydroxyacetophenone, with total yield 24%. All structures of new compounds were confirmed by IR, 1^H NMR and MS.展开更多
The total synthesis of （＋）-8-（3-methylbut-2-enyl）-2-phenyl-2,3-dihydrochromen-4-one and （±）-2-（4-hydroxyphenyl）-8-（3- methylbut-2-enyl）-2,3-dihydrochromen-4-one was first achieved through C-prenylation...The total synthesis of （＋）-8-（3-methylbut-2-enyl）-2-phenyl-2,3-dihydrochromen-4-one and （±）-2-（4-hydroxyphenyl）-8-（3- methylbut-2-enyl）-2,3-dihydrochromen-4-one was first achieved through C-prenylation, protection of phenolic hydroxyl group, aldol condensation, cyclization and deprotection starting from cheap benzaldehyde, 4-hydroxybenzaldehyde and 2-hydroxyace- tophenone, with total yield of 20 and 16.3%. All structures of new compounds were confirmed by IR, 1H NMR and MS. 2009 Jin Hui Yang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
基金We thank the National Natural Science Foundation （No. 20562010）；Ministry of National Education （No.203143）for financial support.
文摘The total synthesis of （±）-abyssinoflavanone V was first achieved through C-prenylation, selective protection of phenolic hydroxyl group, aldol condensation, cyclization and deprotection starting from cheap 4-hydroxybenzaldehyde and 2,4,6- trihydroxyacetophenone, with total yield 24%. All structures of new compounds were confirmed by IR, 1^H NMR and MS.
基金the National Natural Science Foundation(No.20562010)Ministry of National Education(No.203143)for financial support
文摘The total synthesis of （＋）-8-（3-methylbut-2-enyl）-2-phenyl-2,3-dihydrochromen-4-one and （±）-2-（4-hydroxyphenyl）-8-（3- methylbut-2-enyl）-2,3-dihydrochromen-4-one was first achieved through C-prenylation, protection of phenolic hydroxyl group, aldol condensation, cyclization and deprotection starting from cheap benzaldehyde, 4-hydroxybenzaldehyde and 2-hydroxyace- tophenone, with total yield of 20 and 16.3%. All structures of new compounds were confirmed by IR, 1H NMR and MS. 2009 Jin Hui Yang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
