当前位置: X-MOL 学术Heterocycl. Commun. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Asymmetric total synthesis of filamentous fungi related resorcylic acid lactones 7-epi-zeaenol and zeaenol
Heterocyclic Communications ( IF 1.3 ) Pub Date : 2019-05-17 , DOI: 10.1515/hc-2019-0015
Sai Reddy Doda 1 , Avula Raghavendar 2 , Sharath Babu Haridasyam 2 , Chandra Shekar Putta 3 , Bhattu Kanakadurga rao 3 , Sudhakar Kadari 3
Affiliation  

Abstract An efficient, short and, a convenient asymmetric total synthesis of filamentous fungi related resorcylic acid lactones 7-epi-zeaenol (2) and zeaenol (1) have been achieved in 7 and 9 linear steps with the high overall yield of 32% and 21% respectively, from the known intermediate 13. Mitsunobu inversion, De Brabander’s protocol for macrolactonisation, Heck cross-coupling, diastereoselective alkyne aldehyde coupling and Ohira–Bestmann alkynylation are the key reactions.

中文翻译:

丝状真菌相关间苯二酸内酯 7-epi-zeaenol 和 zeaenol 的不对称全合成

摘要 丝状真菌相关间苯二酸内酯 7-epi-zeaenol (2) 和 zeaenol (1) 的高效、短程和方便的不对称全合成已通过 7 和 9 个线性步骤实现,总收率高达 32% 和分别为 21%,来自已知的中间体 13。Mitsunobu 反转、De Brabander 的大环内酯化方案、Heck 交叉偶联、非对映选择性炔醛偶联和 Ohira-Bestmann 炔基化是关键反应。
更新日期:2019-05-17
down
wechat
bug