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4-(6-Benzyloxy-2-(benzyloxycarbonyl)benzoyl)-3,5-dibenzyloxybenzoic Acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158585-06-9

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158585-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158585-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,5,8 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158585-06:
(8*1)+(7*5)+(6*8)+(5*5)+(4*8)+(3*5)+(2*0)+(1*6)=169
169 % 10 = 9
So 158585-06-9 is a valid CAS Registry Number.

158585-06-9Downstream Products

158585-06-9Relevant academic research and scientific papers

Total synthesis of (-)-balanol

Miyabe, Hideto,Torieda, Mayumi,Inoue, Kyoko,Tajiri, Kazumi,Kiguchi, Toshiko,Naito, Takeaki

, p. 4397 - 4407 (2007/10/03)

The efficient total synthesis of (-)-balanol, a potent inhibitor of the protein kinase C, is described (-)-Balanol consists of a chiral hexahydroazepine-containing fragment and a benzophenone fragment, both of which were prepared via novel synthetic routes. The hxahydroazepine fragment was prepared in racemic form through either Bu3SnH- or SmI2-promoted radical cyclization of oxime ethers 2ab intramolecularly connected with the formyl group. SmI2-promoted radical cyclization of 2b was found to be particularly successful in the selective synthesis of the seven-membered trans-amino alcohol 8b. Preparation of the enantiomerically pure hexahydroazepine-containing fragment was achieved through the enantioselective enzymatic acetylation of racemic alcohol 9, employing the immobilized lipase from Pseudomonas sp. The benzophenone fragment was prepared in short steps through a biomimetic oxidative anthraquinone ring cleavage starting from commercially available natural chrysophanic acid 15c. This reaction proceeded via [4 + 2]-cycloaddition of single of oxygen to anthracene derivative 17c, followed by Baeyer-Villiger-type rearrangement of the resulting hydroperoxide to afford the benzophenone derivatives 22 and 23.

Total synthesis of (-)-balanol

Miyabe, Hideto,Torieda, Mayumi,Kiguchi, Toshiko,Naito, Takeaki

, p. 580 - 582 (2007/10/03)

The total synthesis of (-)-balanol, a potent protein kinase C inhibitor, is described. The synthesis includes a radical cyclization approach to the hexahydroazepine-containing fragment and a biomimetic route to the benzophenone fragment.

Total synthesis of (-)· and (+)-balanol

Lampe, John W.,Hughes, Philip F.,Biggers, Christopher K.,Smith, Shelley H.,Hu, Hong

, p. 4572 - 4581 (2007/10/03)

Two total syntheses of the potent protein kinase C inhibitory fungal metabolite balanol are described. In the first approach, the core aminohydroxyazepane subunit was prepared in racemic form by stereospecific functionalization of N-benzyl-∈-caprolactam.

Total synthesis of balanol: a potent protein kinase C inhibitor of fungal origin

Adams, C. P.,Fairway, S. M.,Hardy, C. J.,Hibbs, D. E.,Hursthouse, M. B.,et al.

, p. 2355 - 2362 (2007/10/02)

The total synthesis of the fungal metabolite balanol, a potent inhibitor of protein kinase C, is described.The synthesis includes a novel synthesis of 3-amino-4-hydroxyazepanes via a directed ring expansion of 3-bromopiperidin-4-ones.

Total Synthesis of Balanol and Designed Analogues

Nicolaou, K. C.,Koide, Kazunori,Bunnage, Mark E.

, p. 454 - 466 (2007/10/03)

The total synthesis of balanol, a potent protein kinase C inhibitor isolated from the fungus Verticillium balanoides, is described.The hexahydroazepine fragment was prepared from D-serine through a sequence of reactions including the diastereoselective allylboration of a derived amino aldehyde and a base-induced 7-exo-tet ring closure as key steps.The benzophenone fragment was secured through the initial coupling of the two functionalised aromatic components through an ester linkage, followed by intramolecular nucleophilic attack of an aryl lithium derivative to form the desired ketone bridge.After coupling of the two balanol domains, the adoption of benzyl-derived protecting groups for the latent functionalities then allowed the liberation of balanol in a single step by catalytic hydrogenolysis.Finally, the newly developed synthetic strategy was applied to the synthesis of a variety of designed balanol analogues for biological evaluation. - Keywords: antitumor agents, balanol, enzyme inhibitor, natural product, total synthesis

Total Synthesis of (-)-Balanol

Lampe, John W.,Hughes, Philip F.,Biggers, Christopher K.,Smith, Shelley H.,Hu, Hong

, p. 5147 - 5148 (2007/10/02)

(-)-Balanol, a fungal metabolite with potent protein kinase C inhibitory properties, has been prepared in a total synthesis which makes use of an anionic homo-Fries rearrangement approach to the benzophenone subunit and in which the azepane subunit is obt

Two practical syntheses of sterically congested benzophenones

Hollinshead,Nichols,Wilson

, p. 6703 - 6709 (2007/10/02)

Two efficient syntheses of the sterically congested tetraortho-substituted benzophenone portion of balanol 1 (a potent PKC inhibitor) in a protected form are described. Ortho lithiation reactions are employed for the preparation of the required 1,2,3-tris

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