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Unified strategy

Oltra and Cuerva have reported a unified strategy for the synthesis of the eudesmanolides that relies on the collidine-chlorotrimethylsilane reagent... [Pg.52]

Ciufolini, MA. Shm, Y.-C. Bishop, M.J. (1995) A unified strategy for the synthesis of sulfur-containing pyridoacridine alkaloids antitumor agents of marine origin. J. Am. Chem. Soc., 117,12460-9. [Pg.310]

Feldman KS, Saunders JC, Wrobleski ML (2002) Alkynyliodonium Salts in Organic Synthesis. Development of a Unified Strategy for the Syntheses of (-)-Agelastatin A and (-)-Agelastatin B. J Org Chem 67 7096... [Pg.439]

For an outline of an alternative unified strategy for the synthesis of aryl C-glycosides, see Martin, S. F. Pure AddI. Chem. 2003. 75, 63. [Pg.105]

In the evolution of QSAR models for ecotoxicity, several pathways have been addressed, to better explore the possibilities. The numerous QSAR models (many thousands) have been in some cases organized within a unified strategy of developing an architecture in which several simple models are present. In other cases global models have been developed by way of more... [Pg.639]

There are no grand unifying strategies to make 1,2-disubstituted compounds. Rather there are many diverse methods which I sha]] try to classify in a helpful fashion. Here, even more than elsewhere, it is important to judge each case on its merits. One common theme is a preference for the disconnection (1) of the bond joining the two substituted atoms. [Pg.191]

It is also worth mentioning that mathematical modeling of the process and combustion chamber was so reliable that it could be employed as a powerful design tool to optimize the combustion system avoiding expensive trials (Figure 23.23). Then modeling could be used in conjunction with experiments in a unified strategy for... [Pg.484]

Bisai A, West SP, Sarpong R (2008) Unified strategy for the synthesis of the miscellaneous Lycopodium alkaloids total synthesis of ( )-lyconadin A. J Am Chem Soc 130 7222-7223... [Pg.31]

An interesting Csp -Csp coupling via an aryl radical cyclization has been used as the key step in a unified strategy to synthesize vasconine (22), assoanine (20), oxoassoanine (21), and pratosine. Tin hydride cyclization of an A-(o-bromobenzyl)-aniline yielded a substituted phenanthridine which was subsequently transformed into vasconine (22), from which the remaining natural products were prepared (269) (Scheme 9). [Pg.121]

Gross U, Nieger M, Brase S (2010) A Unified Strategy Targeting the Thiodiketopiperazine Mycotoxins Exserohilone, Gliotoxin, the Epicoccins, the Epicorazines, Rostratin A and Aranotin. Chem Eur J 16 11624... [Pg.254]

Brohmer MC, Bourcet E, Nieger M, Brase S (2011) A Unified Strategy for the Asymmetric S mthesis of Diversonol and Lachnone C. Chem Eur J 49 13706. [Pg.264]

Stark, S., Chernyshenko, O S. and Drasgow, F. 2006. Detecting differential item functioning with confirmatoiy factor analysis and item response theory Toward a unified strategy. Journal of Applied Psychology, 91(6), 1292-306. [Pg.181]

Dickie, R. A., Toward a Unified Strategy of Service Life Prediction, Journal of Coatings Technology, Vol. 64, No. 809, June 1992, pp. 61-64. [Pg.636]

In 2011, Yang and coworkers developed a unified strategy for the synthesis of drimane-type sesquiterpenoids based on an enabling gold-catalyzed tandem reaction (Scheme 13.26) [31], This strategy accomplished the first total synthesis of maras-mene and other analogs of drimane-type sesquiterpenoids. [Pg.388]

Breder A, Chinigo GM, Waltman AW et al (2011) Towards the synthesis of massadine a unified strategy for the stereoselective synthesis of the carbocyclic c, d-ring subunit. Chem Eur J 17 12405-12416... [Pg.180]

GalUgan MJ, Akula R, Ibrahim H (2014) Unified strategy for iodine(III)-mediated halogenation and azidation of 1,3-dieaibonyl eompounds. Org Lett 16(2) 600-603... [Pg.165]

FIGURE 12.3 A unified strategy for alkaloid synthesis completed and almost completed alkaloids... [Pg.320]

As will be discussed, our pivotal intramolecular aza-[3+3] cycloaddition was remarkably efficient in providing the tricyclic scaffold of (—)-cylindricine C 384 and that of putative (—)-lepadiformine 389 (or (—)-4-deoxo-2-epi-cylindricine C) [170b,[198], yet this route could not be implemented in our synthesis of (—)-lepadiformine 385. To reconcile this, we devised a unified strategy to synthesize (—)-lepadiformine and (+)-cylindricines C-E (386-388) that... [Pg.335]

To advance our quest in demonstrating the utility of our pivotal intramolecular aza-[3+3] cycloaddition as a unified strategy to access different Wheterocyclic manifolds known in naturally occurring alkaloids, we synthesized the family of Coccinellidae defensive alkaloids 420 and 426-429 (Figure 12.5) [171]. Our strategy utilizes a common intermediate, the aza-tricyclic core 425, which is attained via an intramolecular aza-[3+3] cycloaddition. [Pg.340]

After our puhhcation of our unified strategy toward (+)-cylindricines C—E and (—)-lepadiformine, Kibayashi published their strategy. See Ref. [201d]. [Pg.354]

Trost BM, MaUiotra S, Chan WH. Exercising regiocontrol in palladium-catalyzed asymmetric prenylations and geranyla-tion unifying strategy toward flustramines A and B. J. Am. Chem. Soc. 2011 133(19) 7328-7331. [Pg.393]

Reiss T, Breit B. A unified strategy for the stereospecific construction of propionates and acetate-propionates relying on a directed allylic substitution. Chem. Eur. J. 2009 15 6345-6348. [Pg.853]


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See also in sourсe #XX -- [ Pg.21 ]




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