✦ LIBER ✦

Total Synthesis of (−)-Salicylihalamide A

✍ Scribed by Snider, Barry B.; Song, Fengbin

Book ID: 120256511
Publisher: American Chemical Society
Year: 2001
Tongue: English
Weight: 73 KB
Volume: 3
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol015822v

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of (-)-Salicylihalamide A.

✍ Barry B. Snider; Fengbin Song 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Total Synthesis of (-)-Salicylihalamide

Total Synthesis of (-)-Salicylihalamide A and Related Congeners.

✍ Amos B. Smith III; Junying Zheng 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 views

ChemInform Abstract: A First Generation

ChemInform Abstract: A First Generation Total Synthesis of (+)-Salicylihalamide A.

✍ Amos B. Smith III; Junying Zheng 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

A Formal Total Synthesis of the Salicyli

A Formal Total Synthesis of the Salicylihalamides

✍ Christian Herb; Martin E. Maier 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 62 KB 👁 1 views

Total Synthesis of Salicylihalamides A a

Total Synthesis of Salicylihalamides A and B

✍ Christian Herb; Alexander Bayer; Martin E. Maier 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 365 KB 👁 2 views

## Abstract The paper illustrates two efficient routes to macrolactone **19** containing a 3‐(__para__‐methoxybenzyloxy)propyl side chain at C‐15. The chiral center at C‐15 was introduced by a Noyori reduction of keto ester **5**. The intermediate common to both routes, aldehyde **8**, was prepared

Enantioselective total synthesis of sali

Enantioselective total synthesis of salicylihalamides A and B

✍ Denis Labrecque; Sylvie Charron; Rabindra Rej; Charles Blais; Serge Lamothe 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 99 KB

We have devised a total synthesis of (12R,13S,15R) salicylihalamides A and B, which allowed revision of the absolute stereochemistry of the natural compounds. The same strategy was then applied to the preparation of naturally occurring salicylihalamides.