跳轉至內容
Merck
  • Synthesis of (+)-patulolide C via an asymmetric hydroformylation/macrocyclization cascade.

Synthesis of (+)-patulolide C via an asymmetric hydroformylation/macrocyclization cascade.

Organic letters (2012-02-07)
Roberto M Risi, Steven D Burke
摘要

A highly atom-economical total synthesis of (+)-patulolide C has been accomplished in three steps from the known (2R)-8-nonyn-2-ol in 49% overall yield and 93% de. A Rh(I)-catalyzed asymmetric hydroformylation (AHF)/ intramolecular Wittig olefination cascade was utilized to set the C4-hydroxyl stereochemistry and E-olefin geometry as well as form the macrolactone.

材料
產品編號
品牌
產品描述

Sigma-Aldrich
乙酸乙烯酯, contains 3-20 ppm hydroquinone as inhibitor, ≥99%
Supelco
乙酸乙烯酯, analytical standard
Supelco
乙酸乙烯酯 溶液, certified reference material, 5000 μg/mL in acetonitrile
乙酸乙烯酯, European Pharmacopoeia (EP) Reference Standard