Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Synthesis of (–)-Muricatacin and (–)-(R,R)-L-Factor Involving an Organocatalytic Direct Vinylogous Aldol Reaction
Synlett ( IF 1.7 ) Pub Date : 2017-08-14 , DOI: 10.1055/s-0036-1590858 Christopher Cooze 1 , Amarender Manchoju 1 , Sunil Pansare 1
Synlett ( IF 1.7 ) Pub Date : 2017-08-14 , DOI: 10.1055/s-0036-1590858 Christopher Cooze 1 , Amarender Manchoju 1 , Sunil Pansare 1
Affiliation
Concise syntheses of the polyketide natural product (–)-muricatacin and (–)-( R , R )-L-factor (natural product enantiomer) were achieved in four steps by employing an organocatalytic asymmetric direct vinylogous aldol reaction of γ-crotonolactone and suitable aliphatic aldehydes as the key step.
中文翻译:
(-)-Muricatacin 和 (-)-(R,R)-L-Factor 的合成涉及有机催化直接 Vinylogous Aldol 反应
聚酮化合物天然产物 (-)-muricatacin 和 (-)-( R , R )-L-因子(天然产物对映异构体)的简明合成是通过采用 γ-巴豆内酯和合适的脂肪醛作为关键步骤。
更新日期:2017-08-14
中文翻译:
(-)-Muricatacin 和 (-)-(R,R)-L-Factor 的合成涉及有机催化直接 Vinylogous Aldol 反应
聚酮化合物天然产物 (-)-muricatacin 和 (-)-( R , R )-L-因子(天然产物对映异构体)的简明合成是通过采用 γ-巴豆内酯和合适的脂肪醛作为关键步骤。