✦ LIBER ✦

The first total synthesis of aplysamine 6, an inhibitor of isoprenylcysteine carboxy methyltransferase

✍ Scribed by Nisar Ullah; Khaled M. Arafeh

Book ID: 104095968
Publisher: Elsevier Science
Year: 2009
Tongue: French
Weight: 146 KB
Volume: 50
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2008.10.103

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

An improved total synthesis of spermatin

An improved total synthesis of spermatinamine, an inhibitor of isoprenylcysteine carboxy methyltransferase

✍ Nisar Ullah; Shamsuddeen A. Haladu; Basem A. Mosa 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 260 KB

Aplysamine 6, an Alkaloidal Inhibitor of

Aplysamine 6, an Alkaloidal Inhibitor of Isoprenylcysteine Carboxyl Methyltransferase from the Sponge Pseudoceratina sp.

✍ Buchanan, Malcolm S.; Carroll, Anthony R.; Fechner, Gregory A.; Boyle, Anthony; 📂 Article 📅 2008 🏛 American Chemical Society 🌐 English ⚖ 57 KB

Total synthesis of the natural isoprenyl

Total synthesis of the natural isoprenylcysteine carboxyl methyltransferase inhibitor spermatinamine

✍ José García; Raquel Pereira; Angel R. de Lera 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 293 KB

with a bromotyrosine-spermine-bromotyrosine dimeric structure is described.

ChemInform Abstract: Spermatinamine, the

ChemInform Abstract: Spermatinamine, the First Natural Product Inhibitor of Isoprenylcysteine Carboxyl Methyltransferase, a New Cancer Target

✍ Ronald J. Quinn; et al. et al. 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 19 KB

The First Total Synthesis of (±)-Terpest

The First Total Synthesis of (±)-Terpestacin, HIV Syncytium Formation Inhibitor

✍ Kuniaki Tatsuta; Naoyuki Masuda; Hidemitsu Nishida 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 600 KB

Terpcstacin has beensynthesizedthroughC-alkylation of ~-ketolactone9 widrchain portion12.'rlresctwocompounds werederivedfrom2-cyclopcrrten-l-ylactic acid andE,E-farnesol, tI?sptXtively. 01997 ElsevierScience Ltd. AU rights reserved. Terpestacin( ) is a bicyclo5-15-fusedsesterterpeneisolatedfromArth

The first total synthesis of novel human

The first total synthesis of novel human chymase inhibitor SPF32629A

✍ Srinivasa Rao Vegi; Shanthaveerappa K. Boovanahalli; Arun Prakash Sharma; K. Muk 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 167 KB

The first total synthesis of SPF32629A, a novel human chymase inhibitor, has been accomplished from the readily available precursor 4-nitropyridine N-oxide, following an efficient strategy with a sequence of eight straightforward steps.