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Nicolaou, K. C. & Montagnon, T. Molecules that Changed the World: A Brief History of the Art and Science of Amalgam and its Impact on Society (Wiley-VCH, 2008).
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Draw The Correct Product For The Following Diels -... | Chegg.com | draw the correct product for the following diels alder reactionNicolaou, K. C. & Sorensen, E. J. Classics in Absolute Amalgam (Wiley-VCH, 1995).
Nicolaou, K. C. & Snyder, S. A. Classics in Absolute Amalgam II (Wiley-VCH, 2003).
Walji, A. M. & MacMillan, D. W. C. Strategies to bypass the Taxol problem. Enantioselective avalanche catalysis, a new admission for the able architecture of atomic complexity. Synlett 1477–1489 (2007).
Staunton, J. & Weissman, K. J. Polyketide biosynthesis: a millennium review. Nature Prod. Rep. 18, 380–416 (2001).
Townsend, C. A. Structural studies of accustomed artefact biosynthetic proteins. Chem. Biol. 4, 721–730 (1997).
Floss, H. G. & Yu. T.-W. Rifamycin-mode of action, resistance, and biosynthesis. Chem. Rev. 105, 621–632 (2005).
Davies, H. M. L. & Sorensen, E. J. Rapid complication bearing in accustomed artefact absolute synthesis. Chem. Soc. Rev. 38, 2981–2982 (2009).
Nicolaou, K. C. & Chen, J. S. The art of absolute amalgam through avalanche reactions. Chem. Soc. Rev. 38, 2993–3009 (2009).
Nicolaou, K. C., Edmonds, D. J. & Bulger, P. G. Avalanche reactions in absolute synthesis. Angew. Chem. Int. Ed. 45, 7134–7186 (2006).
Young, I. S. & Baran, P. S. Protecting-group-free amalgam as an befalling for invention. Nature Chem. 1, 193–205 (2009).
Burns, N. Z., Baran, P. S. & Hoffmann, R. W. Redox abridgement in amoebic synthesis. Angew. Chem. Int. Ed. 48, 2854–2867 (2009).
Trost, B. M. The atom abridgement − a chase for constructed efficiency. Science 254, 1471–1477 (1991).
Wender, P. A., Verma, V. A., Paxton, T. J. & Pillow, T. H. Function-oriented synthesis, footfall economy, and biologic design. Acc. Chem. Res. 41, 40–49 (2008).
Kim, J. & Movassaghi, M. Biogenetically aggressive syntheses of alkaloid accustomed products. Chem. Soc. Rev. 38, 3035–3050 (2009).
Bulger, P. G., Bagal, S. K. & Marquez, R. Recent advances in biomimetic accustomed artefact synthesis. Nat. Prod. Rep. 25, 254–297 (2008).
Newhouse, T., Baran, P. S. & Hoffmann, R. W. The economies of synthesis. Chem. Soc. Rev. 38, 3010–3021 (2009).
Tietze, L. F., Brasche, G. & Gericke, K. M. Domino Reactions in Amoebic Amalgam (Wiley-VCH, 2006).
Enders, D., Grondal, C. & Hüttl, M. R. M. Agee organocatalytic domino reactions. Angew. Chem. Int. Ed. 46, 1570–1581 (2007).
Walji, A. M. & MacMillan, D. W. C. Strategies to bypass the taxol problem. Enantioselective avalanche catalysis, a new admission for the able architecture of atomic complexity. Synlett 1477–1489 (2007).
Bertelsen, S. & Jørgensen, K. A. Organocatalysis - afterwards the gold rush. Chem. Soc. Rev. 38, 2178–2189 (2009).
Dondoni, A. & Massi, A. Agee organocatalysis: from boyhood to adolescence. Angew. Chem. Int. Ed. 47, 4638–4660 (2008).
["1237.72"]
Draw The Correct Product For The Following Diels-A... | Chegg.com | draw the correct product for the following diels alder reactionMacMillan, D. W. C. The appearance and development of organocatalysis. Nature 455, 304–308 (2008).
Dalko, P. I. Enantioselective Organocatalysis, Reactions and Experimental Procedures (Wiley-VCH, 2007).
Organocatalysis. Chem. Rev. 107 (special issue), 5413–5883 (2007).
de Figueiredo, R. M. & Christmann, M. Organocatalytic amalgam of drugs and bioactive accustomed products. Eur. J. Org. Chem. 2575–2600 (2007).
Berkessel, A. & Gröger, H. Agee Organocatalysis (Wiley-VCH, 2005).
Zhang, F.-L., Xu, A.-W., Gong, Y.-F., Wei, M.-H. & Yang, X.-L. Agee organocatalytic four basic quadruple domino acknowledgment accomplished by oxa-Michael accession of alcohols to acrolein. Chem. Eur. J. 15, 6815–6818 (2009).
Kotame, P., Hong, B.-C. & Liao, J.-H. Enantioselective amalgam of the tetrahydro-6H-benzo[c]chromenes via domino Michael–aldol condensation: ascendancy of bristles stereocenters in a quadruple-cascade organocatalytic multi-component reaction. Tetrahedron Lett. 50, 704–707 (2009).
Enders, D., Krüll, R. & Bettray, W. Microwave-assisted organocatalytic quadruple domino reactions of acetaldehyde and nitroalkenes. Amalgam doi:10.1055/s-0029-1217146 (2010).
Akiyama, T., Itoh, J. & Fuchibe, K. Recent advance in chiral Brønsted acerbic catalysis. Adv. Synth. Catal. 348, 999–1010 (2006).
Taylor, M. S. & Jacobsen, E. N. Agee catalysis by chiral hydrogen-bond donors. Angew. Chem. Int. Ed. 45, 1520–1543 (2006).
Enders, D., Niemeier, O. & Henseler, A. Organocatalysis by N-heterocyclic carbenes. Chem. Rev. 107, 5606–5655 (2007).
Lathrop, S. P. & Rovis, T. Agee amalgam of functionalized cyclopentanones via a multicatalytic accessory amine/N-heterocyclic carbene catalyzed avalanche sequence. J. Am. Chem. Soc. 131, 13628–13630 (2009).
Sun, F.-G., Huang, X.-L. & Ye, S. Diastereoselective amalgam of 4-hydroxytetralones via a avalanche Stetter−aldol acknowledgment catalyzed by N-heterocyclic carbenes. J. Org. Chem. 75, 273–276 (2010).
Sánchez-Larios, E. & Gravel, M. Diastereoselective amalgam of indanes via a domino Stetter−Michael reaction. J. Org. Chem. 74, 7536–7539 (2009).
Seebach, D. Methods of acuteness umpolung. Angew. Chem. Int. Ed. Engl. 18, 239–258 (1979).
Kaneko, S., Yoshino, T., Katoh, T. & Terashima, S. Constructed studies of Huperzine A and its fluorinated analogues. 1. Atypical agee syntheses of an enantiomeric brace of Huperzine A. Tetrahedron 54, 5471–5484 (1998).
Bai, D. Development of huperzine A and B for analysis of Alzheimer's disease. Authentic Appl. Chem. 79, 469–479 (2007).
List, B. The ying and yang of agee aminocatalysis. Chem. Commun. 819–824 (2006).
Yua, X. & Wang, W. Organocatalysis: agee avalanche reactions catalysed by chiral accessory amines. Org. Biomol. Chem. 6, 2037–2046 (2008).
Melchiorre, P., Marigo, M., Carlone, A. & Bartoli, G. Agee aminocatalysis - Gold blitz in amoebic chemistry. Angew. Chem. Int. Ed. 47, 6138–6171 (2008).
Marigo, M., Franzén, J., Poulsen, T. B., Zhuang, W. & Jørgensen, K. A. Agee organocatalytic epoxidation of α,β-unsaturated aldehydes with hydrogen peroxide. J. Am. Chem. Soc. 127, 6964–6965 (2005).
["564.54"]
Draw The Correct Product For The Following Diels-A... | Chegg.com | draw the correct product for the following diels alder reactionYang, J. W., Hechavarria Fonseca, M. Y. & List, B. Catalytic agee reductive Michael cyclization. J. Am. Chem. Soc. 127, 15036–15037 (2005).
Huang, Y., Walji, A. M., Larsen, C. H. & MacMillan, D. W. C. Enantioselective organo-cascade catalysis. J. Am. Chem. Soc. 127, 15051–15053 (2005).
Bräse, S., Encinas, A., Keck, J. & Nising, C. F. Allure and analysis of mycotoxins and accompanying fungal metabolites. Chem. Rev. 109, 3903–3990 (2009).
Nising, C. F., Ohnemüller, U. K. & Bräse, S. The absolute amalgam of the fungal metabolite diversonol. Angew. Chem. Int. Ed. 45, 307–309 (2005).
Gérard, E. M. C. & Bräse, S. Modular syntheses of diversonol-type tetrahydroxanthone mycotoxins: blennolide C (epi-hemirugulotrosin A) and analogues. Chem. Eur. J. 14, 8086–8089 (2008).
Ohnemüller, U. K., Nising, C. F., Encinas, A. & Bräse, S. A able admission to enantiomerically authentic 5-substitued 4-hydroxycyclohex-2-enones: An avant-garde hemisecalonic acerbic A model. Amalgam 2175–2185 (2007).
Lesch, B. & Bräse, S. A short, atom-economical access to tetrahydroxanthenones. Angew. Chem. Int. Ed. 43, 115–118 (2003).
Stork, G. & Schultz, A. G. The absolute amalgam of dl-Camptothecin. J. Am. Chem. Soc. 93, 4074–4075 (1971).
Li, Q.-Y., Zu, Y.-G., Shi, R.-Z. & Yao, L.-P. Analysis camptothecin: accepted perspectives. Curr. Med. Chem. 13, 2021–2039 (2006).
Liu, G.-S., Dong, Q.-L., Yao, Y.-S. & Yao, Z.-J. Expeditious absolute syntheses of camptothecin and 10-hydroxycamptothecin. Org. Lett. 10, 5393–5396 (2008).
Dharmarajan, S., Perumal, Y., Rathinasabapathy, T. & Tanushree, R. B. Camptothecin and its analogues: a analysis on their chemotherapeutic potential. Nat. Prod. Res. 19, 393–412 (2005).
Yoshitomi, Y., Arai, H., Makino, K. & Hamada, Y. Enantioselective amalgam of martinelline chiral amount and its diastereomer appliance agee bike Michael–aldol reaction. Tetrahedron 64, 11568–11579 (2008).
Witherup, K. M. et al. Martinelline and martinellic acid, atypical G-protein affiliated receptor antagonists from the close bulb Martinella iquitosensis (bignoniaceae). J. Am. Chem. Soc. 117, 6682–6685 (1995).
Itoh, T., Yokoya, M., Miyauchi, K., Nagata, K. & Ohsawa, A. Absolute amalgam of ent-dihydrocorynantheol by appliance a proline-catalyzed agee accession reaction. Org. Lett. 8, 1533–1535 (2006).
Ibrahem, I., Sundén, H., Rios, R., Zhao, G.-L. & Córdova, A. One-pot pyrrolidine-catalyzed amalgam of benzopyrans, benzothiopyranes, and dihydroquinolidines. Chimia 61, 219–223 (2007).
Bertelsen, S., Marigo, M., Brandes, S., Dinér, P. & Jørgensen, K. A. Dienamine catalysis: organocatalytic agee γ-amination of α, β-unsaturated aldehydes. J. Am. Chem. Soc. 128, 12973–12980 (2006).
Liu, K., Chougnet, A. & Woggon, W.-D. A abbreviate avenue to α-tocopherol. Angew. Chem. Int. Ed. 47, 5827–5829 (2008).
Volz, N., Bröhmer, M. C., Nieger, M. & Bräse, S. Where are they now? An agee organocatalytic arrangement appear 4a-methyl tetrahydroxanthones: academic amalgam of 4-dehydroxydiversonol. Synlett 550–553 (2009).
Hong, B.-C., Wu, M.-F., Tseng, H.-C. & Liao, J.-H. Enantioselective organocatalytic academic [3 3] cycloaddition of α, β-unsaturated aldehydes and appliance to the agee amalgam of (-)-isopulegol hydrate and (-)-cubebaol. Org. Lett. 8, 2217–2220 (2006).
Hong, B.-C. et al. Organocatalytic agee Robinson annulation of α,β-unsaturated aldehydes: applications to the absolute amalgam of ( )-palitantin. J. Org. Chem. 72, 8458–8471 (2007).
Lelais, G. & MacMillan, D. W. C. Modern strategies in amoebic catalysis: the appearance and development of iminium activation. Aldrichimica Acta 39, 79–87 (2006).
["584.91"]
Draw The Correct Product For The Following Diels-A... | Chegg.com | draw the correct product for the following diels alder reactionAustin, J. F., Kim, S.-G., Sinz, C. F., Xiao, W.-J. & MacMillan, D. W. C. Enantioselective organocatalytic architecture of pyrroloindolines by a avalanche addition–cyclization strategy: amalgam of (–)-flustramine B. Proc. Natl Acad. Sci. USA 101, 5483–5487 (2004).
Jones, S. B., Simmons, B. & MacMillan, D. W. C. Nine-step enantioselective absolute amalgam of ( )-minfiensine. J. Am. Chem. Soc. 131, 13606–13607 (2009).
Massiot, G., Thépenier, P., Jacquier, M.-J., Le Men-Olivier, L. & Delaude, C. Normavacurine and minfiensine, two new alkaloids with C19H22N2O blueprint from Strychnos species. Heterocycles 29, 1435–1438 (1989).
Enders, D., Hüttl, M. R. M., Grondal, C. & Raabe, G. Ascendancy of four stereocentres in a amateur avalanche organocatalytic reaction. Nature 441, 861–863 (2006).
Enders, D., Hüttl, M. R. M., Runsink, J., Raabe, G. & Wendt, B. Organocatalytic one-pot agee amalgam of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence. Angew. Chem. Int. Ed. 46, 467–469 (2007).
Enders, D., Hüttl, M. R. M., Raabe, G. & Bats, J. W. Agee amalgam of polyfunctionalized mono-, bi-, and tricyclic carbon frameworks via organocatalytic domino reactions. Adv. Synth. Catal. 350, 267–279 (2008).
Michrowska, A. & List, B. Concise amalgam of ricciocarpin A and analysis of a added almighty analogue. Nature Chem. 1, 225–228 (2009).
Wurzel, G. & Becker, H. Sesquiterpenoids from the liverwort Ricciocarpos natans. Phytochemistry 29, 2565–2568 (1990).
Wurzel, G., Becker, H., Eicher, H. T. & Tiefensee, K. Molluscicidal backdrop of capacity from the liverwort Ricciocarpos natans and of constructed lunularic acerbic derivatives. Planta Med. 56, 444–445 (1990).
Simmons, B., Walji, A. M. & MacMillan, D. W. C. Cycle-specific organocascade catalysis: appliance to olefin hydroamination, hydro-oxidation, and amino-oxidation, and to accustomed artefact synthesis. Angew. Chem. Int. Ed. 48, 4349–4353 (2009).
Beechan, C. M., Djerassi, C. & Eggert, H. Terpenoids-LXXIV: The sesquiterpenes from the bendable apricot sinularia mayi. Tetrahedron 34, 2503–2508 (1978).
Moriera, I. C., Lago, J. H. G., Young, M. C. M. & Roque, N. F. Antifungal aromadendrane sesquiterpenoids from the leaves of Xylopia brasiliensis. J. Braz. Chem. Soc. 14, 828–831 (2003).
Wu, T., Chan, Y. & Leu, Y. The capacity of the basis and axis of Aristolochia heterophylla hemsl. Chem. Pharm. Bull. 3, 357–361 (2000).
Hoffmann, S., Seayad, A. M. & List, B. A able Brønsted acerbic agitator for the organocatalytic agee alteration hydrogenation of imines. Angew. Chem. Int. Ed. 44, 7424–7427 (2005).
Rueping, M., Sugiono, E., Azap, C., Theissmann, T. & Bolte M. Enantioselective Brønsted acerbic catalyzed alteration hydrogenation: organocatalytic abridgement of imines. Org. Lett. 7, 3781–3783 (2005).
Rueping, M., Antonchick, A. P. & Theissmann, T. A Awful enantioselective Brønsted acerbic catalyzed avalanche reaction: organocatalytic alteration hydrogenation of quinolines and their appliance in the amalgam of alkaloids. Angew. Chem. Int. Ed. 45, 3683–3686 (2006).
Rueping, M. & Antonchick, A. P. Organocatalytic enantioselective abridgement of pyridines. Angew. Chem. Int. Ed. 46, 4562–4565 (2007).
Sklenicka, H. M. et al. Stereoselective academic [3 3] cycloaddition admission to cis-1-azadecalins and amalgam of (–)-4a, 8a-diepi-pumiliotoxin C. Evidence for the aboriginal awful stereoselective 6π-electron electrocyclic arena closures of 1-azatrienes. J. Am. Chem. Soc. 124, 10435–10442 (2002).
Shibasaki, M. & Kanai, M. Constructed strategies for oseltamivir phosphate. Eur. J. Org. Chem. 1839–1850 (2008).
Ishikawa, H., Suzuki, T. & Hayashi, Y. High-yielding amalgam of the anti-influenza neuramidase inhibitor (–)-oseltamivir by three “one-pot” operations. Angew. Chem. Int. Ed. 48, 1304–1307 (2009).
Enders, D., Luettgen, K. & Narine, A. A. Agee sulfa-Michael additions. Amalgam 959–980 (2007).
["629.53"]
Draw The Correct Product For The Following Diels-A... | Chegg.com | draw the correct product for the following diels alder reactionHoashi, Y., Yabuta, T. & Takemoto, Y. Bifunctional thiourea-catalyzed enantioselective bifold Michael acknowledgment of γ, δ-unsaturated β-ketoester to nitroalkene: agee amalgam of (–)-epibatidine. Tetrahedron Lett. 45, 9185–9188 (2004).
["600.43"]
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