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Total Synthesis of Amphidinolide T4

✍ Scribed by Alois Fürstner; Christophe Aïssa; Ricardo Riveiros; Jacques Ragot

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
154 KB
Volume
41
Category
Article
ISSN
0044-8249

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📜 SIMILAR VOLUMES

Total Synthesis of Amphidinolide T4.
Total Synthesis of Amphidinolide T4.
✍ Alois Fuerstner; Christophe Aissa; Ricardo Riveiros; Jacques Ragot 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 66 KB
A Concise Total Synthesis of Amphidinoli
A Concise Total Synthesis of Amphidinolide T2
✍ Dr. Huoming Li; Dr. Jinlong Wu; Dr. Jialu Luo; Prof. Dr. Wei-Min Dai 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 223 KB 👁 1 views

RCM + AD = T2: In the presence of the C16-methylene group, regioselective ring-closing metathesis (RCM) formed the (12E)-endocyclic double bond, which underwent Os-catalyzed asymmetric dihydroxylation (AD) to give the desired 12,13-diol intermediate required for the total synthesis of amphidinolide

Total Syntheses of Amphidinolide T1, T3,
Total Syntheses of Amphidinolide T1, T3, T4, and T5.
✍ Christophe Aissa; Ricardo Riveiros; Jacques Ragot; Alois Fuerstner 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 75 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

Total Synthesis of (−)-Amphidinolide E
Total Synthesis of (−)-Amphidinolide E
✍ Chan Hyuk Kim; Hyo Jung An; Won Kyo Shin; Wei Yu; Sang Kook Woo; Soon Kyu Jung; 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 117 KB 👁 1 views

Amphidinolide E (1) is a unique 18-membered macrolide isolated from the Y-5' strain of the dinoflagellate Amphidinium sp. [1] It exhibits cytotoxic activity against L1210 (IC 50 = 2.0 mg mL À1 ) and L5178Y (IC 50 = 4.8 mg mL À1 ) murine leukemia cells in vitro. Owing to its unique structural feature