Skip to search formSkip to main contentSkip to account menu

FR 901483

Known as: FR-901483, FR901483 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Organophosphorus Compounds

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Atom transfer radical cyclization of trichloroacetamides to electron-rich acceptors using Grubbs' catalysts: synthesis of the tricyclic framework of FR901483.
Intramolecular Kharasch-type additions of trichloroacetamides on anisole and enol acetates catalyzed by Grubbs' ruthenium… 
2013
2013
Enantioselective total syntheses of (-)-FR901483 and (+)-8-epi-FR901483.
The enantioselective total syntheses of the potent immunosuppressant FR901483 (1) and its 8-epimer (47) have been accomplished… 
Review
2009
Review
2009
Synthetic Studies of Heterocyclic Natural Products
The methods that were developed for the synthesis of the heterocyclic natural products luotonin A, ophiuroidine, cephalandole B… 
2008
2008
A Synthesis of the Tricyclic Core Structure of FR901483 Featuring an Ugi Four-Component Coupling and a Remarkably Selective Elimination Reaction.
Three key reactions, an efficient Ugi four-component coupling, a regiospecific, base-mediated elimination reaction, and an… 
2007
2007
Toward the total synthesis of FR901483: concise synthesis of the azatricyclic skeleton.
A concise synthesis of the azatricyclic core of FR901483 has been accomplished using a novel strategy that involves a… 
2006
2006
Efficient approach to the Azaspirane core of FR 901483.
[reaction: see text] An efficient approach to the azaspirane core of FR 901483 is described employing lithiated methoxyallene as… 
2006
2006
FR 901483 , a Novel Immunosuppressant Isolated from Cladobotryum sp . No . 11231 Taxonomyof the Producing Organism , Fermentation , Isolation , Physico-chemical Properties and Biological Activities
FR901483, a novel immunosuppressant, has been isolated from the fermentation broth of Cladobotryum sp. No. 11231. The molecular… 
2005
2005
A formal total synthesis of (-)-FR901483, using a tandem cationic aza-Cope rearrangement/Mannich cyclization approach.
A formal total synthesis of the immunosuppressant FR901483 has been accomplished. The key step in the synthesis utilizes a tandem… 
2001
2001
Total synthesis of FR901483.
[structure: see text]. The total synthesis of FR901483, a structurally novel immunosuppressant, has been accomplished by the use… 
2001
2001
Tandem cationic aza-cope rearrangement-Mannich cyclization approach to the core structure of FR901483 via a Bridgehead iminium ion.
[reaction in text] An approach to the potent immunosuppressant FR901483 is described. This route utilizes a tandem cationic aza… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)