메뉴 건너뛰기




Volumn 17, Issue 5, 2015, Pages 253-302

Diversity-oriented approaches to polycyclics and bioinspired molecules via the diels-alder strategy: Green chemistry, synthetic economy, and beyond

Author keywords

amino acids; Diels Alder reaction; dienes; diversity oriented synthesis; green chemistry; polycyclics

Indexed keywords

ALKADIENE; POLYCYCLIC HYDROCARBON;

EID: 84929167417     PISSN: 21568952     EISSN: None     Source Type: Journal    
DOI: 10.1021/co500146u     Document Type: Review
Times cited : (74)

References (288)
  • 1
    • 0001147462 scopus 로고
    • Cycloaddition Reactions in Organic Synthesis
    • Baldwin, J. E. Magnus, P. D. Pergamon: Oxford, UK
    • Carruthers, W. Cycloaddition Reactions in Organic Synthesis. In Tetrahedron Organic Chemistry Series; Baldwin, J. E., Magnus, P. D., Eds.; Pergamon: Oxford, UK, 1990; Vol. 8; pp 1-373.
    • (1990) Tetrahedron Organic Chemistry Series , vol.8 , pp. 1-373
    • Carruthers, W.1
  • 4
    • 84893838561 scopus 로고    scopus 로고
    • Quinones as Dienophiles in the Diels-Alder Reaction: History and Applications in Total Synthesis
    • Nawrat, C. C.; Moody, C. J. Quinones as Dienophiles in the Diels-Alder Reaction: History and Applications in Total Synthesis Angew. Chem., Int. Ed. 2014, 53, 2056-2077
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 2056-2077
    • Nawrat, C.C.1    Moody, C.J.2
  • 5
    • 84875695231 scopus 로고    scopus 로고
    • Industrial Applications of the Diels-Alder Reaction
    • Funel, J.-A.; Abele, S. Industrial Applications of the Diels-Alder Reaction Angew. Chem., Int. Ed. 2013, 52, 3822-3863
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 3822-3863
    • Funel, J.-A.1    Abele, S.2
  • 7
    • 30744456747 scopus 로고    scopus 로고
    • Recent Advances in Natural Product Synthesis by Using Intramolecular Diels-Alder Reactions
    • Takao, K.-i.; Munakata, R.; Tadano, K.-i. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels-Alder Reactions Chem. Rev. 2005, 105, 4779-4806
    • (2005) Chem. Rev. , vol.105 , pp. 4779-4806
    • Takao, K.-I.1    Munakata, R.2    Tadano, K.-I.3
  • 9
    • 4243599124 scopus 로고
    • Progress in the Diels-Alder Reaction Means Progress in Steroid Synthesis
    • Ottow, E. Schollkopf, K. Schulz, B. G. Springer-Verlag: Berlin.
    • Quinkert, G.; del Grosso, M. Progress in the Diels-Alder Reaction Means Progress in Steroid Synthesis. In Stereoselective Synthesis; Ottow, E.; Schollkopf, K.; Schulz, B. G., Eds.; Springer-Verlag: Berlin, 1994.
    • (1994) Stereoselective Synthesis
    • Quinkert, G.1    Del Grosso, M.2
  • 10
    • 70350496831 scopus 로고    scopus 로고
    • Recent Applications of Intramolecular Diels-Alder Reactions to Natural Product Synthesis
    • Juhl, M.; Tanner, D. Recent Applications of Intramolecular Diels-Alder Reactions to Natural Product Synthesis Chem. Soc. Rev. 2009, 38, 2983-2992
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2983-2992
    • Juhl, M.1    Tanner, D.2
  • 12
    • 84962105974 scopus 로고
    • Synthesen in der Hydroaromatischen Reihe
    • Diels, O.; Alder, K. Synthesen in Der Hydroaromatischen Reihe Justus Liebigs Ann. Chem. 1928, 460, 98-122
    • (1928) Justus Liebigs Ann. Chem. , vol.460 , pp. 98-122
    • Diels, O.1    Alder, K.2
  • 14
    • 0039930587 scopus 로고
    • Acceleration and Selectivity Enhancement of Diels-Alder Reactions by Special and Catalytic Methods
    • Pindur, U.; Lutz, G.; Otto, C. Acceleration and Selectivity Enhancement of Diels-Alder Reactions by Special and Catalytic Methods Chem. Rev. 1993, 93, 741-761
    • (1993) Chem. Rev. , vol.93 , pp. 741-761
    • Pindur, U.1    Lutz, G.2    Otto, C.3
  • 15
    • 84880100773 scopus 로고    scopus 로고
    • Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels-Alder Reaction
    • Jiang, X.; Wang, R. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels-Alder Reaction Chem. Rev. 2013, 113, 5515-5546
    • (2013) Chem. Rev. , vol.113 , pp. 5515-5546
    • Jiang, X.1    Wang, R.2
  • 16
    • 0030963855 scopus 로고    scopus 로고
    • RNA-Catalysed Carbon-Carbon Bond Formation
    • Tarasow, T. M.; Tarasow, S. L.; Eaton, B. E. RNA-Catalysed Carbon-Carbon Bond Formation Nature 1997, 389, 54-57
    • (1997) Nature , vol.389 , pp. 54-57
    • Tarasow, T.M.1    Tarasow, S.L.2    Eaton, B.E.3
  • 17
    • 0035804164 scopus 로고    scopus 로고
    • Diels-Alderases
    • Pohnert, G. Diels-Alderases ChemBioChem 2001, 2, 873-875
    • (2001) ChemBioChem , vol.2 , pp. 873-875
    • Pohnert, G.1
  • 18
    • 0033618847 scopus 로고    scopus 로고
    • The Diels-Alder Reaction and Biopolymer Catalysis
    • Tarasow, T. M.; Eaton, B. E. The Diels-Alder Reaction and Biopolymer Catalysis Cell. Mol. Life Sci. 1999, 55, 1463-1472
    • (1999) Cell. Mol. Life Sci. , vol.55 , pp. 1463-1472
    • Tarasow, T.M.1    Eaton, B.E.2
  • 19
    • 0033102314 scopus 로고    scopus 로고
    • A Small Catalytic RNA Motif with Diels-Alderase Activity
    • Seelig, B.; Jäschke, A. A Small Catalytic RNA Motif with Diels-Alderase Activity Chem. Biol. 1999, 6, 167-176
    • (1999) Chem. Biol. , vol.6 , pp. 167-176
    • Seelig, B.1    Jäschke, A.2
  • 21
    • 0034671737 scopus 로고    scopus 로고
    • Enantioselective Ribozyme Catalysis of a Bimolecular Cycloaddition Reaction
    • Seelig, B.; Keiper, S.; Stuhlmann, F.; Jäschke, A. Enantioselective Ribozyme Catalysis of a Bimolecular Cycloaddition Reaction Angew. Chem., Int. Ed. 2000, 39, 4576-4579
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 4576-4579
    • Seelig, B.1    Keiper, S.2    Stuhlmann, F.3    Jäschke, A.4
  • 23
    • 41449109957 scopus 로고    scopus 로고
    • DNA and RNA can be Equally Efficient Catalysts for Carbon-Carbon Bond Formation
    • Chandra, M.; Silverman, S. K. DNA and RNA can be Equally Efficient Catalysts for Carbon-Carbon Bond Formation J. Am. Chem. Soc. 2008, 130, 2936-2937
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 2936-2937
    • Chandra, M.1    Silverman, S.K.2
  • 25
    • 84886145796 scopus 로고    scopus 로고
    • RNA as a Catalyst: The Diels-Alderase Ribozyme
    • Mayer, G. John Wiley & Sons, Ltd. Chichester, UK.
    • Jäschke, A. RNA as a Catalyst: The Diels-Alderase Ribozyme. In The Chemical Biology of Nucleic Acids; Mayer, G., Ed.; John Wiley & Sons, Ltd.: Chichester, UK, 2010.
    • (2010) The Chemical Biology of Nucleic Acids
    • Jäschke, A.1
  • 26
    • 0342974220 scopus 로고
    • Transannular Diels-Alder Reaction on Macrocycles. A General Strategy for the Synthesis of Polycyclic Compounds
    • Deslongchamps, P. Transannular Diels-Alder Reaction on Macrocycles. A General Strategy for the Synthesis of Polycyclic Compounds Pure Appl. Chem. 1992, 64, 1831-1847
    • (1992) Pure Appl. Chem. , vol.64 , pp. 1831-1847
    • Deslongchamps, P.1
  • 27
    • 0035858717 scopus 로고    scopus 로고
    • The Transannular Diels-Alder Strategy: Applications to Total Synthesis
    • Marsault, E.; Toró, A.; Nowak, P.; Deslongchamps, P. The Transannular Diels-Alder Strategy: Applications to Total Synthesis Tetrahedron 2001, 57, 4243-4260
    • (2001) Tetrahedron , vol.57 , pp. 4243-4260
    • Marsault, E.1    Toró, A.2    Nowak, P.3    Deslongchamps, P.4
  • 28
    • 34648829990 scopus 로고    scopus 로고
    • Asymmetric Catalysis of the Transannular Diels-Alder Reaction
    • Balskus, E. P.; Jacobsen, E. N. Asymmetric Catalysis of the Transannular Diels-Alder Reaction Science 2007, 317, 1736-1740
    • (2007) Science , vol.317 , pp. 1736-1740
    • Balskus, E.P.1    Jacobsen, E.N.2
  • 29
    • 77957900964 scopus 로고    scopus 로고
    • Synthesis of a trans, syn, trans-Dodecahydrophenanthrene via a Bicyclic Transannular Diels-Alder Reaction: Intermediate for the Synthesis of Fusidic Acid
    • Jung, M. E.; Zhang, T.-H.; Lui, R. M.; Gutierrez, O.; Houk, K. N. Synthesis of a trans, syn, trans-Dodecahydrophenanthrene via a Bicyclic Transannular Diels-Alder Reaction: Intermediate for the Synthesis of Fusidic Acid J. Org. Chem. 2010, 75, 6933-6940
    • (2010) J. Org. Chem. , vol.75 , pp. 6933-6940
    • Jung, M.E.1    Zhang, T.-H.2    Lui, R.M.3    Gutierrez, O.4    Houk, K.N.5
  • 30
    • 84862562467 scopus 로고    scopus 로고
    • Transannular Diels-Alder Reactivities of 14-Membered Macrocylic Trienes and Their Relationship with the Conformational Preferences of the Reactants: A Combined Quantum Chemical and Molecular Dynamics Study
    • Prathyusha, V.; Ramakrishna, S.; Deva Priyakumar, U. Transannular Diels-Alder Reactivities of 14-Membered Macrocylic Trienes and Their Relationship with the Conformational Preferences of the Reactants: A Combined Quantum Chemical and Molecular Dynamics Study J. Org. Chem. 2012, 77, 5371-5380
    • (2012) J. Org. Chem. , vol.77 , pp. 5371-5380
    • Prathyusha, V.1    Ramakrishna, S.2    Deva Priyakumar, U.3
  • 31
    • 84873325401 scopus 로고    scopus 로고
    • Increasing the Efficiency of the Transannular Diels-Alder Strategy via Palladium(II)-Catalyzed Macrocyclizations
    • Iafe, R. G.; Kuo, J. L.; Hochstatter, D. G.; Saga, T.; Turner, J. W.; Merlic, C. A. Increasing the Efficiency of the Transannular Diels-Alder Strategy via Palladium(II)-Catalyzed Macrocyclizations Org. Lett. 2013, 15, 582-585
    • (2013) Org. Lett. , vol.15 , pp. 582-585
    • Iafe, R.G.1    Kuo, J.L.2    Hochstatter, D.G.3    Saga, T.4    Turner, J.W.5    Merlic, C.A.6
  • 32
    • 84886305653 scopus 로고    scopus 로고
    • Transannular Diels-Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Total Synthesis of a Unique Set of Vinblastine Analogues
    • Campbell, E. L.; Skepper, C. K.; Sankar, K.; Duncan, K. K.; Boger, D. L. Transannular Diels-Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Total Synthesis of a Unique Set of Vinblastine Analogues Org. Lett. 2013, 15, 5306-5309
    • (2013) Org. Lett. , vol.15 , pp. 5306-5309
    • Campbell, E.L.1    Skepper, C.K.2    Sankar, K.3    Duncan, K.K.4    Boger, D.L.5
  • 33
    • 47249130867 scopus 로고    scopus 로고
    • The Dehydro-Diels-Alder Reaction
    • Wessig, P.; Müller, G. The Dehydro-Diels-Alder Reaction Chem. Rev. 2008, 108, 2051-2063
    • (2008) Chem. Rev. , vol.108 , pp. 2051-2063
    • Wessig, P.1    Müller, G.2
  • 34
    • 80055020011 scopus 로고    scopus 로고
    • The Photo-Dehydro-Diels-Alder (PDDA) Reaction
    • Wessig, P.; Matthes, A.; Pick, C. The Photo-Dehydro-Diels-Alder (PDDA) Reaction Org. Biomol. Chem. 2011, 9, 7599-7605
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 7599-7605
    • Wessig, P.1    Matthes, A.2    Pick, C.3
  • 35
    • 84895922525 scopus 로고    scopus 로고
    • Base-Catalyzed Tandem Michael/Dehydro-Diels-Alder Reaction of α,α-Dicyanoolefins with Electron-Deficient 1,3-Conjugated Enynes: A Facile Entry to Angularly Fused Polycycles
    • Zhang, M.; Zhang, J. Base-Catalyzed Tandem Michael/Dehydro-Diels-Alder Reaction of α,α-Dicyanoolefins with Electron-Deficient 1,3-Conjugated Enynes: A Facile Entry to Angularly Fused Polycycles Chem. - Eur. J. 2014, 20, 399-404
    • (2014) Chem. - Eur. J. , vol.20 , pp. 399-404
    • Zhang, M.1    Zhang, J.2
  • 36
    • 84866034566 scopus 로고    scopus 로고
    • A Thermal Dehydrogenative Diels-Alder Reaction of Styrenes for the Concise Synthesis of Functionalized Naphthalenes
    • Kocsis, L. S.; Benedetti, E.; Brummond, K. M. A Thermal Dehydrogenative Diels-Alder Reaction of Styrenes for the Concise Synthesis of Functionalized Naphthalenes Org. Lett. 2012, 14, 4430-4433
    • (2012) Org. Lett. , vol.14 , pp. 4430-4433
    • Kocsis, L.S.1    Benedetti, E.2    Brummond, K.M.3
  • 37
    • 0030724760 scopus 로고    scopus 로고
    • Thermolysis of 1,3,8-Nonatriyne: Evidence for Intramolecular [2 + 4] Cycloaromatization to a Benzyne Intermediate
    • Bradley, A. Z.; Johnson, R. P. Thermolysis of 1,3,8-Nonatriyne: Evidence for Intramolecular [2 + 4] Cycloaromatization to a Benzyne Intermediate J. Am. Chem. Soc. 1997, 119, 9917-9918
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 9917-9918
    • Bradley, A.Z.1    Johnson, R.P.2
  • 38
    • 69949112734 scopus 로고    scopus 로고
    • A Metal-Templated 4 + 2 Cycloaddition Reaction of an Alkyne and a Diyne to Form a 1,2-Aryne
    • Tsui, J. A.; Sterenberg, B. T. A Metal-Templated 4 + 2 Cycloaddition Reaction of an Alkyne and a Diyne To Form a 1,2-Aryne Organometallics 2009, 28, 4906-4908
    • (2009) Organometallics , vol.28 , pp. 4906-4908
    • Tsui, J.A.1    Sterenberg, B.T.2
  • 40
    • 84875172314 scopus 로고    scopus 로고
    • Synthesis of Complex Benzenoids via the Intermediate Generation of o -Benzynes Through the Hexadehydro-Diels-Alder Reaction
    • Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P.; Hoye, T. R. Synthesis of Complex Benzenoids via the Intermediate Generation of o -Benzynes Through the Hexadehydro-Diels-Alder Reaction Nat. Protoc. 2013, 8, 501-508
    • (2013) Nat. Protoc. , vol.8 , pp. 501-508
    • Baire, B.1    Niu, D.2    Willoughby, P.H.3    Woods, B.P.4    Hoye, T.R.5
  • 42
    • 84891800470 scopus 로고    scopus 로고
    • Regioselectivity in the Nucleophile Trapping of Arynes: The Electronic and Steric Effects of Nucleophiles and Substituents
    • Karmakar, R.; Yun, S. Y.; Wang, K.-P.; Lee, D. Regioselectivity in the Nucleophile Trapping of Arynes: The Electronic and Steric Effects of Nucleophiles and Substituents Org. Lett. 2014, 16, 6-9
    • (2014) Org. Lett. , vol.16 , pp. 6-9
    • Karmakar, R.1    Yun, S.Y.2    Wang, K.-P.3    Lee, D.4
  • 43
    • 84891791022 scopus 로고    scopus 로고
    • Dichlorination of (Hexadehydro-Diels-Alder Generated) Benzynes and a Protocol for Interrogating the Kinetic Order of Bimolecular Aryne Trapping Reactions
    • Niu, D.; Wang, T.; Woods, B. P.; Hoye, T. R. Dichlorination of (Hexadehydro-Diels-Alder Generated) Benzynes and a Protocol for Interrogating the Kinetic Order of Bimolecular Aryne Trapping Reactions Org. Lett. 2014, 16, 254-257
    • (2014) Org. Lett. , vol.16 , pp. 254-257
    • Niu, D.1    Wang, T.2    Woods, B.P.3    Hoye, T.R.4
  • 44
    • 84901782644 scopus 로고    scopus 로고
    • The Hexadehydro-Diels-Alder Reaction: A New Chapter in Aryne Chemistry
    • Holden (née Hall), C.; Greaney, M. F. The Hexadehydro-Diels-Alder Reaction: A New Chapter in Aryne Chemistry Angew. Chem., Int. Ed. 2014, 53, 5746-5749
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 5746-5749
    • Holden, C.1    Greaney, M.F.2
  • 45
    • 33748216380 scopus 로고
    • Photo-induced exo-Selective Diels-Alder Reactions
    • Pandey, B.; Dalvi, P. V. Photo-induced exo-Selective Diels-Alder Reactions Angew. Chem., Int. Ed. Engl. 1993, 32, 1612-1613
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 1612-1613
    • Pandey, B.1    Dalvi, P.V.2
  • 46
    • 55449123606 scopus 로고    scopus 로고
    • Exo- and Enantioselective Diels-Alder Reactions: Pyrazolidinone Auxiliaries as a Means to Enhanced Exo Selectivity
    • Sibi, M. P.; Nie, X.; Shackleford, J. P.; Stanley, L. M.; Bouret, F. Exo- and Enantioselective Diels-Alder Reactions: Pyrazolidinone Auxiliaries as a Means to Enhanced Exo Selectivity Synlett 2008, 2655-2658
    • (2008) Synlett , pp. 2655-2658
    • Sibi, M.P.1    Nie, X.2    Shackleford, J.P.3    Stanley, L.M.4    Bouret, F.5
  • 47
    • 34548592016 scopus 로고    scopus 로고
    • Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts
    • Kano, T.; Tanaka, Y.; Maruoka, K. Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts Chem. - Asian J. 2007, 2, 1161-1165
    • (2007) Chem. - Asian J. , vol.2 , pp. 1161-1165
    • Kano, T.1    Tanaka, Y.2    Maruoka, K.3
  • 48
    • 80052455391 scopus 로고    scopus 로고
    • Exo-Selective Asymmetric Diels-Alder Reaction of 2,4-Dienals and Nitroalkenes by Trienamine Catalysis
    • Jia, Z.-J.; Zhou, Q.; Zhou, Q.-Q.; Chen, P.-Q.; Chen, Y.-C. Exo-Selective Asymmetric Diels-Alder Reaction of 2,4-Dienals and Nitroalkenes by Trienamine Catalysis Angew. Chem., Int. Ed. 2011, 50, 8638-8641
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 8638-8641
    • Jia, Z.-J.1    Zhou, Q.2    Zhou, Q.-Q.3    Chen, P.-Q.4    Chen, Y.-C.5
  • 49
    • 34547149552 scopus 로고    scopus 로고
    • Diarylprolinol Silyl Ether as Catalyst of an exo-Selective, Enantioselective Diels-Alder Reaction
    • Gotoh, H.; Hayashi, Y. Diarylprolinol Silyl Ether as Catalyst of an exo-Selective, Enantioselective Diels-Alder Reaction Org. Lett. 2007, 9, 2859-2862
    • (2007) Org. Lett. , vol.9 , pp. 2859-2862
    • Gotoh, H.1    Hayashi, Y.2
  • 50
    • 33746125825 scopus 로고    scopus 로고
    • Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts
    • Kano, T.; Tanaka, Y.; Maruoka, K. Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts Org. Lett. 2006, 8, 2687-2689
    • (2006) Org. Lett. , vol.8 , pp. 2687-2689
    • Kano, T.1    Tanaka, Y.2    Maruoka, K.3
  • 51
    • 0001284159 scopus 로고
    • Exo-Selective Diels-Alder Reaction Based on a Molecular Recognition Approach
    • Maruoka, K.; Imoto, H.; Yamamoto, H. Exo-Selective Diels-Alder Reaction Based on a Molecular Recognition Approach J. Am. Chem. Soc. 1994, 116, 12115-12116
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 12115-12116
    • Maruoka, K.1    Imoto, H.2    Yamamoto, H.3
  • 53
    • 0030748044 scopus 로고    scopus 로고
    • Asymmetric Exo-Selective Diels-Alder Reactions by Steric Attenuation of Secondary Orbital Interactions
    • Powers, T. S.; Jiang, W.; Su, J.; Wulff, W. D.; Waltermire, B. E.; Rheingold, A. L. Asymmetric Exo-Selective Diels-Alder Reactions by Steric Attenuation of Secondary Orbital Interactions J. Am. Chem. Soc. 1997, 119, 6438-6439
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6438-6439
    • Powers, T.S.1    Jiang, W.2    Su, J.3    Wulff, W.D.4    Waltermire, B.E.5    Rheingold, A.L.6
  • 54
    • 67849083450 scopus 로고    scopus 로고
    • Diels-Alder Exo Selectivity in Terminal-Substituted Dienes and Dienophiles: Experimental Discoveries and Computational Explanations
    • Lam, Y.-H.; Cheong, P. H.-Y.; Blasco Mata, J. M.; Stanway, S. J.; Gouverneur, V.; Houk, K. N. Diels-Alder Exo Selectivity in Terminal-Substituted Dienes and Dienophiles: Experimental Discoveries and Computational Explanations J. Am. Chem. Soc. 2009, 131, 1947-1957
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 1947-1957
    • Lam, Y.-H.1    Cheong, P.H.-Y.2    Blasco Mata, J.M.3    Stanway, S.J.4    Gouverneur, V.5    Houk, K.N.6
  • 57
    • 0034678033 scopus 로고    scopus 로고
    • Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery
    • Schreiber, S. L. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery Science 2000, 287, 1964-1969
    • (2000) Science , vol.287 , pp. 1964-1969
    • Schreiber, S.L.1
  • 58
    • 0344515366 scopus 로고    scopus 로고
    • Diversity-Oriented Synthesis; A Challenge for Synthetic Chemists
    • Spring, D. R. Diversity-Oriented Synthesis; A Challenge for Synthetic Chemists Org. Biomol. Chem. 2003, 1, 3867-3870
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 3867-3870
    • Spring, D.R.1
  • 59
    • 3042799070 scopus 로고    scopus 로고
    • A Planning Strategy for Diversity-Oriented Synthesis
    • Burke, M. D.; Schreiber, S. L. A Planning Strategy for Diversity-Oriented Synthesis Angew. Chem., Int. Ed. 2004, 43, 46-58
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 46-58
    • Burke, M.D.1    Schreiber, S.L.2
  • 60
    • 33644839988 scopus 로고    scopus 로고
    • Diversity-Oriented Synthesis: Exploring the Intersections between Chemistry and Biology
    • Tan, D. S. Diversity-Oriented Synthesis: Exploring the Intersections between Chemistry and Biology Nature Chem. Biol. 2005, 1, 74-84
    • (2005) Nature Chem. Biol. , vol.1 , pp. 74-84
    • Tan, D.S.1
  • 61
    • 45149134173 scopus 로고    scopus 로고
    • Diversity Oriented Synthesis of Functionalized Chiral Tetrahydropyridines: Potential GABA Receptor Agonists and Azasugars from Natural Amino Acids via a Sequential Baylis-Hillman Reaction and RCM Protocol
    • Radha Krishna, P.; Srinivas Reddy, P. Diversity Oriented Synthesis of Functionalized Chiral Tetrahydropyridines: Potential GABA Receptor Agonists and Azasugars from Natural Amino Acids via a Sequential Baylis-Hillman Reaction and RCM Protocol J. Comb. Chem. 2008, 10, 426-435
    • (2008) J. Comb. Chem. , vol.10 , pp. 426-435
    • Radha Krishna, P.1    Srinivas Reddy, P.2
  • 62
    • 84862008385 scopus 로고    scopus 로고
    • Diversity-Oriented Synthesis: Producing Chemical Tools for Dissecting Biology
    • O'Connor, C. J.; Beckmann, H. S. G.; Spring, D. R. Diversity-Oriented Synthesis: Producing Chemical Tools for Dissecting Biology Chem. Soc. Rev. 2012, 41, 4444-4456
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 4444-4456
    • O'Connor, C.J.1    Beckmann, H.S.G.2    Spring, D.R.3
  • 65
    • 1442360753 scopus 로고    scopus 로고
    • Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany
    • Grubbs, R. H. Handbook of Metathesis; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2003; Vol. 1-3.
    • (2003) Handbook of Metathesis , vol.13
    • Grubbs, R.H.1
  • 67
    • 36549001142 scopus 로고    scopus 로고
    • Synthesis of Diverse Polycyclic Compounds via Catalytic Metathesis
    • Kotha, S.; Lahiri, K. Synthesis of Diverse Polycyclic Compounds via Catalytic Metathesis Synlett 2007, 2767-2784
    • (2007) Synlett , pp. 2767-2784
    • Kotha, S.1    Lahiri, K.2
  • 68
    • 3343012187 scopus 로고    scopus 로고
    • Olefin Metathesis
    • Grubbs, R. H. Olefin Metathesis Tetrahedron 2004, 60, 7117-7140
    • (2004) Tetrahedron , vol.60 , pp. 7117-7140
    • Grubbs, R.H.1
  • 69
    • 0344006321 scopus 로고    scopus 로고
    • Olefin Metathesis and beyond
    • Fürstner, A. Olefin Metathesis and Beyond Angew. Chem., Int. Ed. 2000, 39, 3012-3043
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3012-3043
    • Fürstner, A.1
  • 70
    • 36049015757 scopus 로고    scopus 로고
    • The Remarkable Metal-Catalysed Olefin Metathesis Reaction
    • Hoveyda, A. H.; Zhugralin, A. R. The Remarkable Metal-Catalysed Olefin Metathesis Reaction Nature 2007, 450, 243-251
    • (2007) Nature , vol.450 , pp. 243-251
    • Hoveyda, A.H.1    Zhugralin, A.R.2
  • 72
    • 82955187545 scopus 로고    scopus 로고
    • Strategies and Tactics in Olefin Metathesis
    • Kotha, S.; Dipak, M. K. Strategies and Tactics in Olefin Metathesis Tetrahedron 2012, 68, 397-421
    • (2012) Tetrahedron , vol.68 , pp. 397-421
    • Kotha, S.1    Dipak, M.K.2
  • 73
    • 84873158280 scopus 로고    scopus 로고
    • Application of Cross Metathesis in Diene and Polyene Synthesis
    • Wojtkielewicz, A. Application of Cross Metathesis in Diene and Polyene Synthesis Curr. Org. Synth. 2013, 10, 43-66
    • (2013) Curr. Org. Synth. , vol.10 , pp. 43-66
    • Wojtkielewicz, A.1
  • 75
    • 84858392228 scopus 로고    scopus 로고
    • Rongalite: A Useful Green Reagent in Organic Synthesis
    • Kotha, S.; Khedkar, P. Rongalite: A Useful Green Reagent in Organic Synthesis Chem. Rev. 2012, 112, 1650-1680
    • (2012) Chem. Rev. , vol.112 , pp. 1650-1680
    • Kotha, S.1    Khedkar, P.2
  • 76
    • 84949117561 scopus 로고    scopus 로고
    • Diversity-Oriented Approach to Unusual Amino Acid Derivatives and Heterocycles via Methyl 2-Acetamidoacrylate and its Congeners
    • Kotha, S.; Bandarugattu, V. B.; Krishna, N. G. Diversity-Oriented Approach to Unusual Amino Acid Derivatives and Heterocycles via Methyl 2-Acetamidoacrylate and its Congeners Tetrahedron 2014, 70, 5361-5384
    • (2014) Tetrahedron , vol.70 , pp. 5361-5384
    • Kotha, S.1    Bandarugattu, V.B.2    Krishna, N.G.3
  • 78
    • 68949195835 scopus 로고    scopus 로고
    • Advanced Approach to Polycyclics by a Synergistic Combination of Enyne Metathesis and Diels-Alder Reaction
    • Kotha, S.; Meshram, M.; Tiwari, A. Advanced Approach to Polycyclics by a Synergistic Combination of Enyne Metathesis and Diels-Alder Reaction Chem. Soc. Rev. 2009, 38, 2065-2092
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2065-2092
    • Kotha, S.1    Meshram, M.2    Tiwari, A.3
  • 80
    • 34250684650 scopus 로고    scopus 로고
    • Synthesis of Novel Quinone-Amino Acid Hybrids via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps
    • Kotha, S.; Mandal, K.; Banerjee, S.; Mobin, S. M. Synthesis of Novel Quinone-Amino Acid Hybrids via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps Eur. J. Org. Chem. 2007, 1244-1255
    • (2007) Eur. J. Org. Chem. , pp. 1244-1255
    • Kotha, S.1    Mandal, K.2    Banerjee, S.3    Mobin, S.M.4
  • 81
    • 76349107118 scopus 로고    scopus 로고
    • Ethyl Isocyanoacetate as a Useful Glycine Equivalent
    • Kotha, S.; Halder, S. Ethyl Isocyanoacetate as a Useful Glycine Equivalent Synlett 2010, 337-354
    • (2010) Synlett , pp. 337-354
    • Kotha, S.1    Halder, S.2
  • 82
    • 0030785271 scopus 로고    scopus 로고
    • Synthesis of Conformationally Constrained α-Amino Acid Derivatives Using Ethyl Isocyanoacetate as Glycine Equivalent
    • Kotha, S.; Brahmachary, E. Synthesis of Conformationally Constrained α-Amino Acid Derivatives Using Ethyl Isocyanoacetate as Glycine Equivalent Bioorg. Med. Chem. Lett. 1997, 7, 2719-2722
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 2719-2722
    • Kotha, S.1    Brahmachary, E.2
  • 83
    • 0042880949 scopus 로고    scopus 로고
    • Enantioselective Amino Acid Synthesis by Chiral Phase-Transfer Catalysis
    • Maruoka, K.; Ooi, T. Enantioselective Amino Acid Synthesis by Chiral Phase-Transfer Catalysis Chem. Rev. 2003, 103, 3013-3028
    • (2003) Chem. Rev. , vol.103 , pp. 3013-3028
    • Maruoka, K.1    Ooi, T.2
  • 84
    • 4143049107 scopus 로고    scopus 로고
    • The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters
    • O'Donnell, M. J. The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters Acc. Chem. Res. 2004, 37, 506-517
    • (2004) Acc. Chem. Res. , vol.37 , pp. 506-517
    • O'Donnell, M.J.1
  • 85
    • 34447272888 scopus 로고    scopus 로고
    • Recent Advances in Asymmetric Phase-Transfer Catalysis
    • Ooi, T.; Maruoka, K. Recent Advances in Asymmetric Phase-Transfer Catalysis Angew. Chem., Int. Ed. 2007, 46, 4222-4266
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 4222-4266
    • Ooi, T.1    Maruoka, K.2
  • 86
    • 84876234339 scopus 로고    scopus 로고
    • Recent Developments in Asymmetric Phase-Transfer Reactions
    • Shirakawa, S.; Maruoka, K. Recent Developments in Asymmetric Phase-Transfer Reactions Angew. Chem., Int. Ed. 2013, 52, 4312-4348
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 4312-4348
    • Shirakawa, S.1    Maruoka, K.2
  • 87
    • 84891042286 scopus 로고    scopus 로고
    • Cinchona-Derived Chiral Phase-Transfer Catalysts for Amino Acid Synthesis
    • Maruoka, K. Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany.
    • Ooi, T. Cinchona-Derived Chiral Phase-Transfer Catalysts for Amino Acid Synthesis. In Asymmetric Phase-Transfer Catalysis; Maruoka, K., Ed.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2008.
    • (2008) Asymmetric Phase-Transfer Catalysis
    • Ooi, T.1
  • 89
    • 33947508615 scopus 로고    scopus 로고
    • A Facile Synthesis of Ethyl 2-Acetamido-4-methylenehex-5-enoate, a Versatile Diels-Alder Synthon for the Parallel Synthesis of Novel α-Amino Acid Derivatives
    • Chen, R.; Lee, V.; Adlington, R. M.; Baldwin, J. E. A Facile Synthesis of Ethyl 2-Acetamido-4-methylenehex-5-enoate, a Versatile Diels-Alder Synthon for the Parallel Synthesis of Novel α-Amino Acid Derivatives Synthesis 2007, 113-117
    • (2007) Synthesis , pp. 113-117
    • Chen, R.1    Lee, V.2    Adlington, R.M.3    Baldwin, J.E.4
  • 90
    • 84859011942 scopus 로고    scopus 로고
    • Synthesis of Modified Phenylalanine Peptides by Cross Enyne Metathesis and a Diels-Alder Reaction as Key Steps
    • Kotha, S.; Goyal, D.; Thota, N.; Srinivas, V. Synthesis of Modified Phenylalanine Peptides by Cross Enyne Metathesis and a Diels-Alder Reaction as Key Steps Eur. J. Org. Chem. 2012, 1843-1850
    • (2012) Eur. J. Org. Chem. , pp. 1843-1850
    • Kotha, S.1    Goyal, D.2    Thota, N.3    Srinivas, V.4
  • 91
    • 0034124909 scopus 로고    scopus 로고
    • Synthesis of Unusual α-Amino Acid Derivatives via Cross-Enyne Metathesis Reaction
    • Kotha, S.; Halder, S.; Brahmachary, E.; Ganesh, T. Synthesis of Unusual α-Amino Acid Derivatives via Cross-Enyne Metathesis Reaction Synlett 2000, 853-855
    • (2000) Synlett , pp. 853-855
    • Kotha, S.1    Halder, S.2    Brahmachary, E.3    Ganesh, T.4
  • 92
    • 0037020810 scopus 로고    scopus 로고
    • Synthesis of Highly Functionalized Phenylalanine Derivatives via Cross-Enyne Metathesis Reactions
    • Kotha, S.; Halder, S.; Brahmachary, E. Synthesis of Highly Functionalized Phenylalanine Derivatives via Cross-Enyne Metathesis Reactions Tetrahedron 2002, 58, 9203-9208
    • (2002) Tetrahedron , vol.58 , pp. 9203-9208
    • Kotha, S.1    Halder, S.2    Brahmachary, E.3
  • 93
    • 84923275687 scopus 로고    scopus 로고
    • Diversity Oriented Approach to Phenylalanine Derivatives via the Diels-Alder Reaction Involving Sulfolene Intermediates
    • Kotha, S.; Vijayalaxmi, B. Diversity Oriented Approach to Phenylalanine Derivatives via the Diels-Alder Reaction Involving Sulfolene Intermediates Heterocycles 2015, 90, 226-237
    • (2015) Heterocycles , vol.90 , pp. 226-237
    • Kotha, S.1    Vijayalaxmi, B.2
  • 94
    • 33750717840 scopus 로고    scopus 로고
    • Total Synthesis and Biological Evaluation of Viscolin, A 1,3-Diphenylpropane as a Novel Potent Anti-Inflammatory Agent
    • Su, C.-R.; Shen, Y.-C.; Kuo, P.-C.; Leu, Y.-L.; Damu, A. G.; Wang, Y.-H.; Wu, T.-S. Total Synthesis and Biological Evaluation of Viscolin, A 1,3-Diphenylpropane as a Novel Potent Anti-Inflammatory Agent Bioorg. Med. Chem. Lett. 2006, 16, 6155-6160
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 6155-6160
    • Su, C.-R.1    Shen, Y.-C.2    Kuo, P.-C.3    Leu, Y.-L.4    Damu, A.G.5    Wang, Y.-H.6    Wu, T.-S.7
  • 95
    • 33749049578 scopus 로고    scopus 로고
    • Viscolin, a New Chalcone from Viscum Coloratum, Inhibits Human Neutrophil Superoxide Anion and Elastase Release via a Camp-Dependent Pathway
    • Hwang, T.-L.; Leu, Y.-L.; Kao, S.-H.; Tang, M.-C.; Chang, H.-L. Viscolin, a New Chalcone from Viscum Coloratum, Inhibits Human Neutrophil Superoxide Anion and Elastase Release via a Camp-Dependent Pathway Free Radical Biol. Med. 2006, 41, 1433-1441
    • (2006) Free Radical Biol. Med. , vol.41 , pp. 1433-1441
    • Hwang, T.-L.1    Leu, Y.-L.2    Kao, S.-H.3    Tang, M.-C.4    Chang, H.-L.5
  • 97
    • 60849130694 scopus 로고    scopus 로고
    • A Diversity-Oriented Approach to Diphenylalkanes by Strategic Utilization of [2 + 2 + 2] Cyclotrimerization, Cross-Enyne Metathesis and Diels-Alder Reaction
    • Kotha, S.; Khedkar, P. A Diversity-Oriented Approach to Diphenylalkanes by Strategic Utilization of [2 + 2 + 2] Cyclotrimerization, Cross-Enyne Metathesis and Diels-Alder Reaction Eur. J. Org. Chem. 2009, 730-738
    • (2009) Eur. J. Org. Chem. , pp. 730-738
    • Kotha, S.1    Khedkar, P.2
  • 98
    • 77953518547 scopus 로고    scopus 로고
    • Design and Synthesis of Benzosultine-sulfone as an o -Xylylene Precursor via Cross-Enyne Metathesis and Rongalite: Further Expansion to Polycyclics via Regioselective Diels-Alder Reaction
    • Kotha, S.; Chavan, A. S. Design and Synthesis of Benzosultine-sulfone as an o -Xylylene Precursor via Cross-Enyne Metathesis and Rongalite: Further Expansion to Polycyclics via Regioselective Diels-Alder Reaction J. Org. Chem. 2010, 75, 4319-4322
    • (2010) J. Org. Chem. , vol.75 , pp. 4319-4322
    • Kotha, S.1    Chavan, A.S.2
  • 99
    • 80053104330 scopus 로고    scopus 로고
    • Diversity-Oriented Synthesis of Biaryl Derivatives Using Cross-Enyne Metathesis, Diels-Alder Reaction, and Suzuki-Miyaura Cross-Coupling as Key Steps
    • Kotha, S.; Vittal, S. Diversity-Oriented Synthesis of Biaryl Derivatives Using Cross-Enyne Metathesis, Diels-Alder Reaction, and Suzuki-Miyaura Cross-Coupling as Key Steps Synlett 2011, 2329-2334
    • (2011) Synlett , pp. 2329-2334
    • Kotha, S.1    Vittal, S.2
  • 100
    • 84924908908 scopus 로고    scopus 로고
    • Diversity-Oriented Approach to Polycyclics via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps
    • Kotha, S.; Vittal, S.; Banerjee, S.; Dipak, M. K. Diversity-Oriented Approach to Polycyclics via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps J. Chem. Sci. 2015, 127, 155-162
    • (2015) J. Chem. Sci. , vol.127 , pp. 155-162
    • Kotha, S.1    Vittal, S.2    Banerjee, S.3    Dipak, M.K.4
  • 101
    • 0037175592 scopus 로고    scopus 로고
    • Recent Applications of the Suzuki-Miyaura Cross-Coupling Reaction in Organic Synthesis
    • Kotha, S.; Lahiri, K.; Kashinath, D. Recent Applications of the Suzuki-Miyaura Cross-Coupling Reaction in Organic Synthesis Tetrahedron 2002, 58, 9633-9695
    • (2002) Tetrahedron , vol.58 , pp. 9633-9695
    • Kotha, S.1    Lahiri, K.2    Kashinath, D.3
  • 102
    • 34250614404 scopus 로고    scopus 로고
    • Expanding the Diversity of Polycyclic Aromatics through a Suzuki-Miyaura Cross-Coupling Strategy
    • Kotha, S.; Lahiri, K. Expanding the Diversity of Polycyclic Aromatics through a Suzuki-Miyaura Cross-Coupling Strategy Eur. J. Org. Chem. 2007, 1221-1236
    • (2007) Eur. J. Org. Chem. , pp. 1221-1236
    • Kotha, S.1    Lahiri, K.2
  • 103
    • 62749140780 scopus 로고    scopus 로고
    • A Retrospective on the Design and Synthesis of Novel Molecules Through a Strategic Consideration of Metathesis and Suzuki-Miyaura Cross-Coupling
    • Kotha, S.; Mandal, K. A Retrospective on the Design and Synthesis of Novel Molecules Through a Strategic Consideration of Metathesis and Suzuki-Miyaura Cross-Coupling Chem. - Asian J. 2009, 4, 354-362
    • (2009) Chem. - Asian J. , vol.4 , pp. 354-362
    • Kotha, S.1    Mandal, K.2
  • 104
    • 34548746810 scopus 로고    scopus 로고
    • Metathesis of a Novel Dienediyne System: A Unique Example Involving the Usage of in Situ Generated Ethylene as Cross-Enyne Metathesis Partner
    • Kotha, S.; Mandal, K. Metathesis of a Novel Dienediyne System: A Unique Example Involving the Usage of In Situ Generated Ethylene as Cross-Enyne Metathesis Partner J. Organomet. Chem. 2007, 692, 4921-4927
    • (2007) J. Organomet. Chem. , vol.692 , pp. 4921-4927
    • Kotha, S.1    Mandal, K.2
  • 105
    • 0037059439 scopus 로고    scopus 로고
    • Syntheses of Anolignans A and B Using Ruthenium-Catalyzed Cross-Enyne Metathesis
    • Mori, M.; Tonogaki, K.; Nishiguchi, N. Syntheses of Anolignans A and B Using Ruthenium-Catalyzed Cross-Enyne Metathesis J. Org. Chem. 2002, 67, 224-226
    • (2002) J. Org. Chem. , vol.67 , pp. 224-226
    • Mori, M.1    Tonogaki, K.2    Nishiguchi, N.3
  • 106
    • 0028103876 scopus 로고
    • New Lignans from Anogeissus Acuminata with HIV-1 Reverse Transcriptase Inhibitory Activity
    • Rimando, A. M.; Pezzuto, J. M.; Farnsworth, N. R. New Lignans from Anogeissus Acuminata with HIV-1 Reverse Transcriptase Inhibitory Activity J. Nat. Prod. 1994, 57, 896-904
    • (1994) J. Nat. Prod. , vol.57 , pp. 896-904
    • Rimando, A.M.1    Pezzuto, J.M.2    Farnsworth, N.R.3
  • 107
    • 33947604111 scopus 로고    scopus 로고
    • A New Versatile Strategy for C-Aryl Glycosides
    • Kaliappan, K. P.; Subrahmanyam, A. V. A New Versatile Strategy for C-Aryl Glycosides Org. Lett. 2007, 9, 1121-1124
    • (2007) Org. Lett. , vol.9 , pp. 1121-1124
    • Kaliappan, K.P.1    Subrahmanyam, A.V.2
  • 108
    • 77954842290 scopus 로고    scopus 로고
    • Application of an Enyne Metathesis/Diels-Alder Cycloaddition Sequence: A New Versatile Approach to the Syntheses of C -Aryl Glycosides and Spiro- C -Aryl Glycosides
    • Subrahmanyam, A. V.; Palanichamy, K.; Kaliappan, K. P. Application of an Enyne Metathesis/Diels-Alder Cycloaddition Sequence: A New Versatile Approach to the Syntheses of C -Aryl Glycosides and Spiro- C -Aryl Glycosides Chem. - Eur. J. 2010, 16, 8545-8556
    • (2010) Chem. - Eur. J. , vol.16 , pp. 8545-8556
    • Subrahmanyam, A.V.1    Palanichamy, K.2    Kaliappan, K.P.3
  • 109
    • 54249086260 scopus 로고    scopus 로고
    • A Rapid Access to New Fluorinated 1,3-Dienes and Benzylic Fluorides via Metathesis on Propargylic Fluorides
    • Pujari, S. A.; Kaliappan, K. P.; Valleix, A.; Grée, D.; Grée, R. A Rapid Access to New Fluorinated 1,3-Dienes and Benzylic Fluorides via Metathesis on Propargylic Fluorides Synlett 2008, 2503-2507
    • (2008) Synlett , pp. 2503-2507
    • Pujari, S.A.1    Kaliappan, K.P.2    Valleix, A.3    Grée, D.4    Grée, R.5
  • 111
    • 84865201967 scopus 로고    scopus 로고
    • 1,7-Octadiene-Assisted Tandem Multicomponent Cross-Enyne Metathesis (CEYM)/Diels-Alder Reactions: A Useful Alternative to Mori's Conditions
    • Fustero, S.; Bello, P.; Miró, J.; Simón, A.; del Pozo, C. 1,7-Octadiene-Assisted Tandem Multicomponent Cross-Enyne Metathesis (CEYM)/Diels-Alder Reactions: A Useful Alternative to Mori's Conditions Chem. - Eur. J. 2012, 18, 10991-10997
    • (2012) Chem. - Eur. J. , vol.18 , pp. 10991-10997
    • Fustero, S.1    Bello, P.2    Miró, J.3    Simón, A.4    Del Pozo, C.5
  • 112
    • 84880388408 scopus 로고    scopus 로고
    • A Ruthenium-Based Catalytic System with Switchable Selectivity between Cyclotrimerization and Enyne Metathesis/Diels-Alder Reactions of Terminal Alkynes
    • Karabulut, S.; Sariaslan, B.; Öztürk, B. Ö. A Ruthenium-Based Catalytic System with Switchable Selectivity Between Cyclotrimerization and Enyne Metathesis/Diels-Alder Reactions of Terminal Alkynes Catal. Commun. 2013, 41, 12-16
    • (2013) Catal. Commun. , vol.41 , pp. 12-16
    • Karabulut, S.1    Sariaslan, B.2    Öztürk, B.O.3
  • 113
    • 0022785312 scopus 로고
    • Total Synthesis of Anthracyclinone
    • Krohn, K. Total Synthesis of Anthracyclinone Angew. Chem., Int. Ed. Engl. 1986, 25, 790-807
    • (1986) Angew. Chem., Int. Ed. Engl. , vol.25 , pp. 790-807
    • Krohn, K.1
  • 114
    • 0001331945 scopus 로고
    • Discovery and Development of Anthracycline Antitumour Antibiotics
    • Lown, J. W. Discovery and Development of Anthracycline Antitumour Antibiotics Chem. Soc. Rev. 1993, 22, 165-176
    • (1993) Chem. Soc. Rev. , vol.22 , pp. 165-176
    • Lown, J.W.1
  • 115
    • 0036158328 scopus 로고    scopus 로고
    • Enantioselective Synthesis of (+)-4-Demethoxy-1,4-dimethyldaunomycinone
    • Kotha, S.; Stoodely, R. J. Enantioselective Synthesis of (+)-4-Demethoxy-1,4-dimethyldaunomycinone Bioorg. Med. Chem. 2002, 10, 621-624
    • (2002) Bioorg. Med. Chem. , vol.10 , pp. 621-624
    • Kotha, S.1    Stoodely, R.J.2
  • 116
    • 78650178911 scopus 로고    scopus 로고
    • Synthetic Approach to cis - And trans -Decalins via Diels-Alder Reaction and Ring-Closing Metathesis as Key Steps: Further Extension to Dioxapropellane Derivative by Ring-Closing Metathesis
    • Kotha, S.; Chavan, A. S.; Dipak, M. K. Synthetic Approach to cis-and trans -Decalins via Diels-Alder Reaction and Ring-Closing Metathesis as Key Steps: Further Extension to Dioxapropellane Derivative by Ring-Closing Metathesis Tetrahedron 2011, 67, 501-504
    • (2011) Tetrahedron , vol.67 , pp. 501-504
    • Kotha, S.1    Chavan, A.S.2    Dipak, M.K.3
  • 117
    • 64549135853 scopus 로고    scopus 로고
    • Benzofurans as Efficient Dienophiles in Normal Electron Demand [4 + 2] Cycloadditions
    • Chopin, N.; Gérard, H.; Chataigner, I.; Piettre, S. R. Benzofurans as Efficient Dienophiles in Normal Electron Demand [4 + 2] Cycloadditions J. Org. Chem. 2009, 74, 1237-1246
    • (2009) J. Org. Chem. , vol.74 , pp. 1237-1246
    • Chopin, N.1    Gérard, H.2    Chataigner, I.3    Piettre, S.R.4
  • 118
    • 78650178039 scopus 로고    scopus 로고
    • Synthesis of (E)-1-Benzyloxy-3-fluoro-1,3-butadiene: A Novel Fluorinated Diene for Diels-Alder Reactions
    • Hayashi, T.; Usuki, Y.; Wakamatsu, Y.; Iio, H. Synthesis of (E)-1-Benzyloxy-3-fluoro-1,3-butadiene: A Novel Fluorinated Diene for Diels-Alder Reactions Synlett 2010, 2843-2846
    • (2010) Synlett , pp. 2843-2846
    • Hayashi, T.1    Usuki, Y.2    Wakamatsu, Y.3    Iio, H.4
  • 119
    • 84879307969 scopus 로고    scopus 로고
    • Two Approaches to the Aromatic Core of the Aminonaphthoquinone Antibiotics
    • Nawrat, C. C.; Palmer, L. I.; Blake, A. J.; Moody, C. J. Two Approaches to the Aromatic Core of the Aminonaphthoquinone Antibiotics J. Org. Chem. 2013, 78, 5587-5603
    • (2013) J. Org. Chem. , vol.78 , pp. 5587-5603
    • Nawrat, C.C.1    Palmer, L.I.2    Blake, A.J.3    Moody, C.J.4
  • 120
    • 0000123574 scopus 로고    scopus 로고
    • Preparation and Diels-Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes
    • Kozmin, S. A.; Rawal, V. H. Preparation and Diels-Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes J. Org. Chem. 1997, 62, 5252-5253
    • (1997) J. Org. Chem. , vol.62 , pp. 5252-5253
    • Kozmin, S.A.1    Rawal, V.H.2
  • 121
    • 0030871612 scopus 로고    scopus 로고
    • Asymmetric Diels-Alder Reactions of Chiral 1-Amino-3-siloxy-1,3-butadiene: Application to the Enantioselective Synthesis of (-)-α-Elemene
    • Kozmin, S. A.; Rawal, V. H. Asymmetric Diels-Alder Reactions of Chiral 1-Amino-3-siloxy-1,3-butadiene: Application to the Enantioselective Synthesis of (-)-α-Elemene J. Am. Chem. Soc. 1997, 119, 7165-7166
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 7165-7166
    • Kozmin, S.A.1    Rawal, V.H.2
  • 123
    • 0036570864 scopus 로고    scopus 로고
    • An Efficient Approach to Aspidosperma Alkaloids via [4 + 2] Cycloadditions of Aminosiloxydienes: Stereocontrolled Total Synthesis of (±)-Tabersonine. Gram-Scale Catalytic Asymmetric Syntheses of (+)-Tabersonine and (+)-16-Methoxytabersonine. Asymmetric Syntheses of (+)-Aspidospermidine and (-)-Quebrachamine
    • Kozmin, S. A.; Iwama, T.; Huang, Y.; Rawal, V. H. An Efficient Approach to Aspidosperma Alkaloids via [4 + 2] Cycloadditions of Aminosiloxydienes: Stereocontrolled Total Synthesis of (±)-Tabersonine. Gram-Scale Catalytic Asymmetric Syntheses of (+)-Tabersonine and (+)-16-Methoxytabersonine. Asymmetric Syntheses of (+)-Aspidospermidine and (-)-Quebrachamine J. Am. Chem. Soc. 2002, 124, 4628-4641
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 4628-4641
    • Kozmin, S.A.1    Iwama, T.2    Huang, Y.3    Rawal, V.H.4
  • 124
    • 70349131589 scopus 로고    scopus 로고
    • Practical Synthesis and Highly Diastereoselective Diels-Alder Reactions of 1-Alkylthio-3-silyloxybutadienes
    • Holmes, J. M.; Albert, A. L.; Gravel, M. Practical Synthesis and Highly Diastereoselective Diels-Alder Reactions of 1-Alkylthio-3-silyloxybutadienes J. Org. Chem. 2009, 74, 6406-6409
    • (2009) J. Org. Chem. , vol.74 , pp. 6406-6409
    • Holmes, J.M.1    Albert, A.L.2    Gravel, M.3
  • 125
    • 0038053109 scopus 로고    scopus 로고
    • Alkynylboronic Esters as Efficient Dienophiles in Cobalt-Catalyzed Diels-Alder Reactions
    • Hilt, G.; Smolko, K. I. Alkynylboronic Esters as Efficient Dienophiles in Cobalt-Catalyzed Diels-Alder Reactions Angew. Chem., Int. Ed. 2003, 42, 2795-2797
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 2795-2797
    • Hilt, G.1    Smolko, K.I.2
  • 126
    • 20744433957 scopus 로고    scopus 로고
    • Dihydroaromatic Boronic Esters as Building Blocks for the Synthesis of Phenanthrenes and Phenanthridines
    • Hilt, G.; Hess, W.; Schmidt, F. Dihydroaromatic Boronic Esters as Building Blocks for the Synthesis of Phenanthrenes and Phenanthridines Eur. J. Org. Chem. 2005, 2526-2533
    • (2005) Eur. J. Org. Chem. , pp. 2526-2533
    • Hilt, G.1    Hess, W.2    Schmidt, F.3
  • 128
    • 62149106948 scopus 로고    scopus 로고
    • Regiocontrolled Cobalt-Catalyzed Diels-Alder Reactions of Silicon-Functionalized, Terminal, and Internal Alkynes
    • Hilt, G.; Janikowski, J. Regiocontrolled Cobalt-Catalyzed Diels-Alder Reactions of Silicon-Functionalized, Terminal, and Internal Alkynes Org. Lett. 2009, 11, 773-776
    • (2009) Org. Lett. , vol.11 , pp. 773-776
    • Hilt, G.1    Janikowski, J.2
  • 129
    • 79951836111 scopus 로고    scopus 로고
    • Regiodiverse Three-Component Synthesis of Arenes
    • Danz, M.; Hilt, G. Regiodiverse Three-Component Synthesis of Arenes Adv. Synth. Catal. 2011, 353, 303-308
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 303-308
    • Danz, M.1    Hilt, G.2
  • 130
    • 84859853689 scopus 로고    scopus 로고
    • Straightforward Synthesis of Nonconjugated Cyclohex-3-enone and Conjugated 4-Methylenecyclohex-2-enone Derivatives
    • Kuttner, J.-R.; Warratz, S.; Hilt, G. Straightforward Synthesis of Nonconjugated Cyclohex-3-enone and Conjugated 4-Methylenecyclohex-2-enone Derivatives Synthesis 2012, 1293-1303
    • (2012) Synthesis , pp. 1293-1303
    • Kuttner, J.-R.1    Warratz, S.2    Hilt, G.3
  • 132
    • 84884555599 scopus 로고    scopus 로고
    • Synthesis of Fluorenone and Anthraquinone Derivatives from Aryl- and Aroyl-Substituted Propiolates
    • Pünner, F.; Schieven, J.; Hilt, G. Synthesis of Fluorenone and Anthraquinone Derivatives from Aryl- and Aroyl-Substituted Propiolates Org. Lett. 2013, 15, 4888-4891
    • (2013) Org. Lett. , vol.15 , pp. 4888-4891
    • Pünner, F.1    Schieven, J.2    Hilt, G.3
  • 134
    • 0035804403 scopus 로고    scopus 로고
    • Dendralenes: The Breakthrough
    • Hopf, H. Dendralenes: The Breakthrough Angew. Chem., Int. Ed. 2001, 40, 705-707
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 705-707
    • Hopf, H.1
  • 135
    • 67650497848 scopus 로고    scopus 로고
    • Forgotten Hydrocarbons Prepared
    • Hopf, H. Forgotten Hydrocarbons Prepared Nature 2009, 460, 183-184
    • (2009) Nature , vol.460 , pp. 183-184
    • Hopf, H.1
  • 136
    • 84857946726 scopus 로고    scopus 로고
    • Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity
    • Hopf, H.; Sherburn, M. S. Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity Angew. Chem., Int. Ed. 2012, 51, 2298-2338
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 2298-2338
    • Hopf, H.1    Sherburn, M.S.2
  • 137
  • 138
    • 0000439081 scopus 로고    scopus 로고
    • Indium-Mediated γ-Pentadienylation of Aldehydes and Ketones: Cross-Conjugated Trienes for Diene-Transmissive Cycloadditions
    • Woo, S.; Squires, N.; Fallis, A. G. Indium-Mediated γ-Pentadienylation of Aldehydes and Ketones: Cross-Conjugated Trienes for Diene-Transmissive Cycloadditions Org. Lett. 1999, 1, 573-576
    • (1999) Org. Lett. , vol.1 , pp. 573-576
    • Woo, S.1    Squires, N.2    Fallis, A.G.3
  • 139
    • 0037073206 scopus 로고    scopus 로고
    • Skeletal Diversity via a Branched Pathway: Efficient Synthesis of 29400 Discrete, Polycyclic Compounds and Their Arraying into Stock Solutions
    • Kwon, O.; Park, S. B.; Schreiber, S. L. Skeletal Diversity via a Branched Pathway: Efficient Synthesis of 29400 Discrete, Polycyclic Compounds and Their Arraying into Stock Solutions J. Am. Chem. Soc. 2002, 124, 13402-13404
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13402-13404
    • Kwon, O.1    Park, S.B.2    Schreiber, S.L.3
  • 140
    • 33744941610 scopus 로고    scopus 로고
    • A Consecutive Diels-Alder Approach Toward a Tet Repressor Directed Combinatorial Library
    • Kormann, C.; Heinemann, F. W.; Gmeiner, P. A Consecutive Diels-Alder Approach Toward a Tet Repressor Directed Combinatorial Library Tetrahedron 2006, 62, 6899-6908
    • (2006) Tetrahedron , vol.62 , pp. 6899-6908
    • Kormann, C.1    Heinemann, F.W.2    Gmeiner, P.3
  • 141
    • 80052951954 scopus 로고    scopus 로고
    • Synthesis of Substituted [3]Dendralenes and Their Unique Cycloaddition Reactions
    • Singh, R.; Ghosh, S. K. Synthesis of Substituted [3]Dendralenes and Their Unique Cycloaddition Reactions Chem. Commun. 2011, 47, 10809-10811
    • (2011) Chem. Commun. , vol.47 , pp. 10809-10811
    • Singh, R.1    Ghosh, S.K.2
  • 142
    • 79953236981 scopus 로고    scopus 로고
    • Highly Functionalized, Angularly Anellated Aromatic Compounds from Dendralenes
    • Hopf, H.; Yildizhan, S. Highly Functionalized, Angularly Anellated Aromatic Compounds from Dendralenes Eur. J. Org. Chem. 2011, 2029-2034
    • (2011) Eur. J. Org. Chem. , pp. 2029-2034
    • Hopf, H.1    Yildizhan, S.2
  • 143
    • 84870663214 scopus 로고    scopus 로고
    • Synthesis of a Potent Antimalarial Amphilectene
    • Pronin, S. V.; Shenvi, R. A. Synthesis of a Potent Antimalarial Amphilectene J. Am. Chem. Soc. 2012, 134, 19604-19606
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 19604-19606
    • Pronin, S.V.1    Shenvi, R.A.2
  • 144
    • 84869159340 scopus 로고    scopus 로고
    • Nitroso-Dienophile Additions to Dendralenes: A Short Synthesis of Branched Aminosugars
    • Wang, R.; Bojase, G.; Willis, A. C.; Paddon-Row, M. N.; Sherburn, M. S. Nitroso-Dienophile Additions to Dendralenes: A Short Synthesis of Branched Aminosugars Org. Lett. 2012, 14, 5652-5655
    • (2012) Org. Lett. , vol.14 , pp. 5652-5655
    • Wang, R.1    Bojase, G.2    Willis, A.C.3    Paddon-Row, M.N.4    Sherburn, M.S.5
  • 145
    • 84873398391 scopus 로고    scopus 로고
    • 3-Bromopenta-2,4-dienylsilane: A Useful Reagent for the Preparation of [3]Dendralenes and Polycyclic Compounds
    • Rahif, M.; Roux, M.; Thibonnet, J.; Parrain, J.-L. 3-Bromopenta-2,4-dienylsilane: A Useful Reagent for the Preparation of [3]Dendralenes and Polycyclic Compounds Mol. Divers. 2013, 17, 49-53
    • (2013) Mol. Divers. , vol.17 , pp. 49-53
    • Rahif, M.1    Roux, M.2    Thibonnet, J.3    Parrain, J.-L.4
  • 147
    • 0000670716 scopus 로고
    • Nouvelle Methode Pour Porter au Maximum la Purete Optique D'un Produit Partiellement Dedouble Sans L'aide D'aucune Substance Chirale
    • Vigneron, J. P.; Dhaenens, M.; Horeau, A. Nouvelle Methode Pour Porter au Maximum la Purete Optique D'un Produit Partiellement Dedouble Sans L'aide D'aucune Substance Chirale Tetrahedron 1973, 29, 1055-1059
    • (1973) Tetrahedron , vol.29 , pp. 1055-1059
    • Vigneron, J.P.1    Dhaenens, M.2    Horeau, A.3
  • 149
    • 0032482523 scopus 로고    scopus 로고
    • Synthesis of Constrained α-Amino Acid Derivatives via Diels-Alder Approach
    • Kotha, S.; Brahmachary, E.; Sreenivasachary, N. Synthesis of Constrained α-Amino Acid Derivatives via Diels-Alder Approach Tetrahedron Lett. 1998, 39, 4095-4098
    • (1998) Tetrahedron Lett. , vol.39 , pp. 4095-4098
    • Kotha, S.1    Brahmachary, E.2    Sreenivasachary, N.3
  • 150
    • 0035898249 scopus 로고    scopus 로고
    • Synthesis of Benzocycloheptene-Based Amino Acid Derivatives via a [4 + 2] Cycloaddition Reaction as a Key Step
    • Kotha, S.; Sreenivasachary, N.; Brahmachary, E. Synthesis of Benzocycloheptene-Based Amino Acid Derivatives via a [4 + 2] Cycloaddition Reaction as a Key Step Tetrahedron 2001, 57, 6261-6265
    • (2001) Tetrahedron , vol.57 , pp. 6261-6265
    • Kotha, S.1    Sreenivasachary, N.2    Brahmachary, E.3
  • 151
  • 152
  • 153
    • 84864074706 scopus 로고    scopus 로고
    • Diversity Oriented Approach to Crownophanes by Enyne Metathesis and Diels-Alder Reaction as Key Steps
    • Kotha, S.; Waghule, G. T. Diversity Oriented Approach to Crownophanes by Enyne Metathesis and Diels-Alder Reaction as Key Steps J. Org. Chem. 2012, 77, 6314-6318
    • (2012) J. Org. Chem. , vol.77 , pp. 6314-6318
    • Kotha, S.1    Waghule, G.T.2
  • 154
    • 23744463470 scopus 로고    scopus 로고
    • Domino Coupling Relay Approach to Polycyclic Pyrrole-2-carboxylates
    • Yamamoto, Y.; Hayashi, H.; Saigoku, T.; Nishiyama, H. Domino Coupling Relay Approach to Polycyclic Pyrrole-2-carboxylates J. Am. Chem. Soc. 2005, 127, 10804-10805
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10804-10805
    • Yamamoto, Y.1    Hayashi, H.2    Saigoku, T.3    Nishiyama, H.4
  • 155
    • 0000450167 scopus 로고    scopus 로고
    • O -Quinodimethanes: Efficient Intermediates in Organic Synthesis
    • Segura, J. L.; Martin, N. o -Quinodimethanes: Efficient Intermediates in Organic Synthesis Chem. Rev. 1999, 99, 3199-3246
    • (1999) Chem. Rev. , vol.99 , pp. 3199-3246
    • Segura, J.L.1    Martin, N.2
  • 156
  • 158
    • 85065852858 scopus 로고
    • Intramolecular Cycloaddition Reactions of ortho-Quinodimethanes in Organic Synthesis
    • Oppolzer, W. Intramolecular Cycloaddition Reactions of ortho-Quinodimethanes in Organic Synthesis Synthesis 1978, 793-802
    • (1978) Synthesis , pp. 793-802
    • Oppolzer, W.1
  • 159
    • 3342991480 scopus 로고    scopus 로고
    • Generation and Cycloaddition of o -Quinodimethane in Aqueous Medium
    • Bieber, L. W.; Da Silva, M. F. Generation and Cycloaddition of o -Quinodimethane in Aqueous Medium Molecules 2001, 6, 472-476
    • (2001) Molecules , vol.6 , pp. 472-476
    • Bieber, L.W.1    Da Silva, M.F.2
  • 160
    • 33751500734 scopus 로고
    • A Convenient Synthesis of 1,4-Dihydro-2,3-Benzoxathiin 3-Oxide, A Useful Precursor of o -Quinodimethane
    • Hoey, M. D.; Dittmer, D. C. A Convenient Synthesis of 1,4-Dihydro-2,3-Benzoxathiin 3-Oxide, A Useful Precursor of o -Quinodimethane J. Org. Chem. 1991, 56, 1947-1948
    • (1991) J. Org. Chem. , vol.56 , pp. 1947-1948
    • Hoey, M.D.1    Dittmer, D.C.2
  • 161
    • 0034618229 scopus 로고    scopus 로고
    • Diels-Alder Approach to Tetralin-Based Constrained α-Amino Acid Derivatives
    • Kotha, S.; Ganesh, T.; Ghosh, A. K. Diels-Alder Approach to Tetralin-Based Constrained α-Amino Acid Derivatives Bioorg. Med. Chem. Lett. 2000, 10, 1755-1757
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1755-1757
    • Kotha, S.1    Ganesh, T.2    Ghosh, A.K.3
  • 162
    • 1642309197 scopus 로고    scopus 로고
    • The Diels-Alder Approach for the Synthesis of Tetralin-Based α-Amino Acid Derivatives and their Modification by the Suzuki-Miyaura Cross-Coupling Reaction
    • Kotha, S.; Ghosh, A. K. The Diels-Alder Approach for the Synthesis of Tetralin-Based α-Amino Acid Derivatives and their Modification by the Suzuki-Miyaura Cross-Coupling Reaction Synthesis 2004, 558-567
    • (2004) Synthesis , pp. 558-567
    • Kotha, S.1    Ghosh, A.K.2
  • 163
    • 84863927924 scopus 로고    scopus 로고
    • Diversity Oriented Approach to Polycyclic Compounds through the Diels-Alder Reaction and the Suzuki Coupling
    • Kotha, S.; Misra, S.; Srinivas, V. Diversity Oriented Approach to Polycyclic Compounds through the Diels-Alder Reaction and the Suzuki Coupling Eur. J. Org. Chem. 2012, 4052-4062
    • (2012) Eur. J. Org. Chem. , pp. 4052-4062
    • Kotha, S.1    Misra, S.2    Srinivas, V.3
  • 164
    • 79952758389 scopus 로고    scopus 로고
    • Synthesis of Polycyclic Aromatics from a Diiodosultine by Suzuki-Miyaura Cross-Coupling and Diels-Alder Reaction
    • Kotha, S.; Meshram, M. Synthesis of Polycyclic Aromatics from a Diiodosultine by Suzuki-Miyaura Cross-Coupling and Diels-Alder Reaction Heterocycles 2011, 82, 1663-1668
    • (2011) Heterocycles , vol.82 , pp. 1663-1668
    • Kotha, S.1    Meshram, M.2
  • 165
    • 1642399542 scopus 로고    scopus 로고
    • A Diels-Alder Approach for the Synthesis of Highly Functionalized Benzo-Annulated Indane-Based α-Amino Acid Derivatives via a Sultine Intermediate
    • Kotha, S.; Ghosh, A. K. A Diels-Alder Approach for the Synthesis of Highly Functionalized Benzo-Annulated Indane-Based α-Amino Acid Derivatives via a Sultine Intermediate Tetrahedron Lett. 2004, 45, 2931-2934
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2931-2934
    • Kotha, S.1    Ghosh, A.K.2
  • 166
    • 14344253325 scopus 로고    scopus 로고
    • Cycloaddition Approach to Benzo-Annulated Indane-Based α-Amino Acid Derivatives
    • Kotha, S.; Ghosh, A. K. Cycloaddition Approach to Benzo-Annulated Indane-Based α-Amino Acid Derivatives Tetrahedron 2004, 60, 10833-10841
    • (2004) Tetrahedron , vol.60 , pp. 10833-10841
    • Kotha, S.1    Ghosh, A.K.2
  • 167
    • 72449148320 scopus 로고    scopus 로고
    • Synthesis of Non-Proteinogenic Phenylalanine Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition Reactions
    • Garcia, L.; Pla-Quintana, A.; Roglans, A. Synthesis of Non-Proteinogenic Phenylalanine Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition Reactions Org. Biomol. Chem. 2009, 7, 5020-5027
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 5020-5027
    • Garcia, L.1    Pla-Quintana, A.2    Roglans, A.3
  • 168
    • 34848908965 scopus 로고    scopus 로고
    • Synthesis of Indanones via Solid-Supported [2 + 2 + 2] Cyclotrimerization
    • Senaiar, R. S.; Teske, J. A.; Young, D. D.; Deiters, A. Synthesis of Indanones via Solid-Supported [2 + 2 + 2] Cyclotrimerization J. Org. Chem. 2007, 72, 7801-7804
    • (2007) J. Org. Chem. , vol.72 , pp. 7801-7804
    • Senaiar, R.S.1    Teske, J.A.2    Young, D.D.3    Deiters, A.4
  • 170
    • 0033590932 scopus 로고    scopus 로고
    • Medicinal Chemistry with Fullerenes and Fullerene Derivatives
    • Da Ros, T.; Prato, M. Medicinal Chemistry with Fullerenes and Fullerene Derivatives Chem. Commun. 1999, 663-669
    • (1999) Chem. Commun. , pp. 663-669
    • Da Ros, T.1    Prato, M.2
  • 171
    • 0037195722 scopus 로고    scopus 로고
    • Synthesis and Characterization of Mono- and Bis-methano[60]fullerenyl Amino Acid Derivatives and Their Reductive Ring-Opening Retro-Bingel Reactions
    • Burley, G. A.; Keller, P. A.; Pyne, S. G.; Ball, G. E. Synthesis and Characterization of Mono- and Bis-methano[60]fullerenyl Amino Acid Derivatives and Their Reductive Ring-Opening Retro-Bingel Reactions J. Org. Chem. 2002, 67, 8316-8330
    • (2002) J. Org. Chem. , vol.67 , pp. 8316-8330
    • Burley, G.A.1    Keller, P.A.2    Pyne, S.G.3    Ball, G.E.4
  • 172
    • 34247153415 scopus 로고    scopus 로고
    • Synthesis of Novel 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid Derivatives Through the Application of Rongalite: A Synergistic Combination of [2 + 2 + 2]- and [4 + 2] Cycloaddition Reactions
    • Kotha, S.; Banerjee, S. Synthesis of Novel 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid Derivatives Through the Application of Rongalite: A Synergistic Combination of [2 + 2 + 2]- and [4 + 2] Cycloaddition Reactions Synthesis 2007, 1015-1020
    • (2007) Synthesis , pp. 1015-1020
    • Kotha, S.1    Banerjee, S.2
  • 173
    • 0034601143 scopus 로고    scopus 로고
    • A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-Carboxylic Acid (Tic) Derivatives via a [2 + 2 + 2] Cycloaddition Reaction
    • Kotha, S.; Sreenivasachary, N. A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-Carboxylic Acid (Tic) Derivatives via a [2 + 2 + 2] Cycloaddition Reaction Bioorg. Med. Chem. Lett. 2000, 10, 1413-1415
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1413-1415
    • Kotha, S.1    Sreenivasachary, N.2
  • 174
    • 40949129637 scopus 로고    scopus 로고
    • Ruthenium-Catalyzed Cyclotrimerization of 1,6- and 1,7-Azadiynes: New Access to Fluorinated Bicyclic Amino Acids
    • Shchetnikov, G. T.; Osipov, S. N.; Bruneau, C.; Dixneuf, P. H. Ruthenium-Catalyzed Cyclotrimerization of 1,6- and 1,7-Azadiynes: New Access to Fluorinated Bicyclic Amino Acids Synlett 2008, 578-582
    • (2008) Synlett , pp. 578-582
    • Shchetnikov, G.T.1    Osipov, S.N.2    Bruneau, C.3    Dixneuf, P.H.4
  • 175
    • 36448995803 scopus 로고    scopus 로고
    • Synthesis of Crown-Based Sulfones via Rongalite: Diversity-Oriented Approach to Annulated Benzocrowns by Diels-Alder Reactions
    • Kotha, S.; Kashinath, D.; Khedkar, P. Synthesis of Crown-Based Sulfones via Rongalite: Diversity-Oriented Approach to Annulated Benzocrowns by Diels-Alder Reactions Synthesis 2007, 3357-3360
    • (2007) Synthesis , pp. 3357-3360
    • Kotha, S.1    Kashinath, D.2    Khedkar, P.3
  • 176
    • 0346522068 scopus 로고    scopus 로고
    • The Synthesis of Naphthosultine and Benzodisultines and Their Pyrolysis with Dienophiles: Studies on o -Naphthoquinodimethane and Bis- o -Quinodimethane
    • Wu, A.-T.; Liu, W.-D.; Chung, W.-S. The Synthesis of Naphthosultine and Benzodisultines and Their Pyrolysis with Dienophiles: Studies on o -Naphthoquinodimethane and Bis- o -Quinodimethane J. Chin. Chem. Soc. 2002, 49, 77-82
    • (2002) J. Chin. Chem. Soc. , vol.49 , pp. 77-82
    • Wu, A.-T.1    Liu, W.-D.2    Chung, W.-S.3
  • 177
    • 0038558792 scopus 로고
    • Condensed Cyclobutane Aromatic Compounds. XI. Benzo[1,2:4,5]dicyclobutene
    • Cava, M. P.; Deana, A. A.; Muth, K. Condensed Cyclobutane Aromatic Compounds. XI. Benzo[1,2:4,5]dicyclobutene J. Am. Chem. Soc. 1960, 82, 2524-2525
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 2524-2525
    • Cava, M.P.1    Deana, A.A.2    Muth, K.3
  • 179
    • 0035924931 scopus 로고    scopus 로고
    • Recent Chemistry of Benzocyclobutenes
    • Mehta, G.; Kotha, S. Recent Chemistry of Benzocyclobutenes Tetrahedron 2001, 57, 625-659
    • (2001) Tetrahedron , vol.57 , pp. 625-659
    • Mehta, G.1    Kotha, S.2
  • 180
    • 68049089944 scopus 로고    scopus 로고
    • Differential Reactivity Pattern of Hybrid o -Quinodimethane Precursors: Strategic Expansion to Annulated Benzocycloalkanes via Rongalite
    • Kotha, S.; Khedkar, P. Differential Reactivity Pattern of Hybrid o -Quinodimethane Precursors: Strategic Expansion to Annulated Benzocycloalkanes via Rongalite J. Org. Chem. 2009, 74, 5667-5670
    • (2009) J. Org. Chem. , vol.74 , pp. 5667-5670
    • Kotha, S.1    Khedkar, P.2
  • 181
    • 80755171506 scopus 로고    scopus 로고
    • Synthetic Approach to Linearly Annulated Tetralin-Based Constrained α-Amino Acid Derivatives via Rongalite
    • Kotha, S.; Krishna, N. G. Synthetic Approach to Linearly Annulated Tetralin-Based Constrained α-Amino Acid Derivatives via Rongalite Curr. Sci. 2011, 101, 923-926
    • (2011) Curr. Sci. , vol.101 , pp. 923-926
    • Kotha, S.1    Krishna, N.G.2
  • 182
    • 84901643580 scopus 로고    scopus 로고
    • Synthesis of Novel Fluoranthene-Based Conformationally Constrained α-Amino Acid Derivatives and Polycyclic Aromatics via the Diels-Alder Reaction
    • Kotha, S.; Meshram, M. Synthesis of Novel Fluoranthene-Based Conformationally Constrained α-Amino Acid Derivatives and Polycyclic Aromatics via the Diels-Alder Reaction Synthesis 2014, 1525-1531
    • (2014) Synthesis , pp. 1525-1531
    • Kotha, S.1    Meshram, M.2
  • 183
    • 84881522076 scopus 로고    scopus 로고
    • Diversity-Oriented Approach to Novel Spirocyclics via Enyne Metathesis, Diels-Alder Reaction, and a [2 + 2 + 2] Cycloaddition as Key Steps
    • Kotha, S.; Ali, R.; Tiwari, A. Diversity-Oriented Approach to Novel Spirocyclics via Enyne Metathesis, Diels-Alder Reaction, and a [2 + 2 + 2] Cycloaddition as Key Steps Synlett 2013, 1921-1926
    • (2013) Synlett , pp. 1921-1926
    • Kotha, S.1    Ali, R.2    Tiwari, A.3
  • 184
    • 84923095923 scopus 로고    scopus 로고
    • Diversity-Oriented Approach to Linearly Fused Spirocycles via Strategic Utilization of a [2 + 2 + 2] Cycloaddition and the Diels-Alder Reaction
    • Kotha, S.; Ali, R. Diversity-Oriented Approach to Linearly Fused Spirocycles via Strategic Utilization of a [2 + 2 + 2] Cycloaddition and the Diels-Alder Reaction Tetrahedron 2015, 71, 1597-1603
    • (2015) Tetrahedron , vol.71 , pp. 1597-1603
    • Kotha, S.1    Ali, R.2
  • 185
    • 84987616126 scopus 로고    scopus 로고
    • Diversity Oriented Approach to Spirobarbituric Acid Derivatives via a [2 + 2 + 2] Cycloaddition and Diels-Alder Reaction as Key Steps
    • Kotha, S.; Ali, R. Diversity Oriented Approach to Spirobarbituric Acid Derivatives via a [2 + 2 + 2] Cycloaddition and Diels-Alder Reaction as Key Steps Heterocycles 2014, 88, 789-797
    • (2014) Heterocycles , vol.88 , pp. 789-797
    • Kotha, S.1    Ali, R.2
  • 186
    • 84923284136 scopus 로고    scopus 로고
    • Diversity-Oriented Approach to Oxepine Derivatives: Further Expansion via Diels-Alder Reaction
    • Kotha, S.; Ali, R. Diversity-Oriented Approach to Oxepine Derivatives: Further Expansion via Diels-Alder Reaction Heterocycles 2015, 90, 645-658
    • (2015) Heterocycles , vol.90 , pp. 645-658
    • Kotha, S.1    Ali, R.2
  • 187
    • 0034595627 scopus 로고    scopus 로고
    • The Syntheses of Pyrazino-Containing Sultines and Their Application in Diels-Alder Reactions with Electron-Poor Olefins and [60]Fullerene
    • Liu, J.-H.; Wu, A.-T.; Huang, M.-H.; Wu, C.-W.; Chung, W.-S. The Syntheses of Pyrazino-Containing Sultines and Their Application in Diels-Alder Reactions with Electron-Poor Olefins and [60]Fullerene J. Org. Chem. 2000, 65, 3395-3403
    • (2000) J. Org. Chem. , vol.65 , pp. 3395-3403
    • Liu, J.-H.1    Wu, A.-T.2    Huang, M.-H.3    Wu, C.-W.4    Chung, W.-S.5
  • 188
    • 0028791849 scopus 로고
    • A Facile Formation of Electroactive Fullerene Adducts from Sultines via a Diels-Alder Reaction
    • Illescas, B.; Martín, N.; Seoane, C.; de la Cruz, P.; Langa, F.; Wudl, F. A Facile Formation of Electroactive Fullerene Adducts from Sultines via a Diels-Alder Reaction Tetrahedron Lett. 1995, 36, 8307-8310
    • (1995) Tetrahedron Lett. , vol.36 , pp. 8307-8310
    • Illescas, B.1    Martín, N.2    Seoane, C.3    De La Cruz, P.4    Langa, F.5    Wudl, F.6
  • 189
    • 0000037595 scopus 로고    scopus 로고
    • Reaction of C60 with Sultines: Synthesis, Electrochemistry, and Theoretical Calculations of Organofullerene Acceptors
    • Illescas, B. M.; Martín, N.; Seoane, C.; Orti, E.; Viruela, P. M.; Viruela, R.; de la Hoz, A. Reaction of C60 with Sultines: Synthesis, Electrochemistry, and Theoretical Calculations of Organofullerene Acceptors J. Org. Chem. 1997, 62, 7585-7591
    • (1997) J. Org. Chem. , vol.62 , pp. 7585-7591
    • Illescas, B.M.1    Martín, N.2    Seoane, C.3    Orti, E.4    Viruela, P.M.5    Viruela, R.6    De La Hoz, A.7
  • 190
    • 33845184269 scopus 로고
    • Syntheses and Electrochemical Properties of Tetracyano- p -Quinodimethane Derivatives Containing Fused Aromatic Rings
    • Martín, N.; Behnisch, R.; Hanack, M. Syntheses and Electrochemical Properties of Tetracyano- p -Quinodimethane Derivatives Containing Fused Aromatic Rings J. Org. Chem. 1989, 54, 2563-2568
    • (1989) J. Org. Chem. , vol.54 , pp. 2563-2568
    • Martín, N.1    Behnisch, R.2    Hanack, M.3
  • 191
    • 37049071580 scopus 로고
    • N, N ′-Dicyanoquinone Diimines (DCNQIs): Unique Acceptors for Conducting Materials
    • Hünig, S. N, N ′-Dicyanoquinone Diimines (DCNQIs): Unique Acceptors for Conducting Materials J. Mater. Chem. 1995, 5, 1469-1479
    • (1995) J. Mater. Chem. , vol.5 , pp. 1469-1479
    • Hünig, S.1
  • 193
    • 33845949270 scopus 로고    scopus 로고
    • Modular Synthesis of Tetrahydrofluorenones from 5-Alkylidene Meldrum's Acids
    • Fillion, E.; Dumas, A. M.; Hogg, S. A. Modular Synthesis of Tetrahydrofluorenones from 5-Alkylidene Meldrum's Acids J. Org. Chem. 2006, 71, 9899-9902
    • (2006) J. Org. Chem. , vol.71 , pp. 9899-9902
    • Fillion, E.1    Dumas, A.M.2    Hogg, S.A.3
  • 194
    • 77954736355 scopus 로고    scopus 로고
    • Facile Access to Boryltetralins and Borylnaphthalenes via a Cycloaddition Using o -Quinodimethanes
    • Yoshida, H.; Mukae, M.; Ohshita, J. Facile Access to Boryltetralins and Borylnaphthalenes via a Cycloaddition Using o -Quinodimethanes Chem. Commun. 2010, 46, 5253-5255
    • (2010) Chem. Commun. , vol.46 , pp. 5253-5255
    • Yoshida, H.1    Mukae, M.2    Ohshita, J.3
  • 195
    • 0041967557 scopus 로고    scopus 로고
    • Highly Enantioselective Diels-Alder Reaction of a Photochemically Generated o -Quinodimethane with Olefins
    • Grosch, B.; Orlebar, C. N.; Herdtweck, E.; Massa, W.; Bach, T. Highly Enantioselective Diels-Alder Reaction of a Photochemically Generated o -Quinodimethane with Olefins Angew. Chem., Int. Ed. 2003, 42, 3693-3696
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 3693-3696
    • Grosch, B.1    Orlebar, C.N.2    Herdtweck, E.3    Massa, W.4    Bach, T.5
  • 196
    • 33745400676 scopus 로고    scopus 로고
    • Enantioselective Diels-Alder Reaction of o -Quinodimethanes by Utilizing Tartaric Acid Ester as a Chiral Auxiliary
    • Takinami, M.; Ukaji, Y.; Inomata, K. Enantioselective Diels-Alder Reaction of o -Quinodimethanes by Utilizing Tartaric Acid Ester as a Chiral Auxiliary Tetrahedron: Asymmetry 2006, 17, 1554-1560
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1554-1560
    • Takinami, M.1    Ukaji, Y.2    Inomata, K.3
  • 197
    • 34248680992 scopus 로고    scopus 로고
    • Diastereoselective Cycloaddition of Chiral 1-Acryloyl-2-Imidazolidinone and o -Quinodimethane Generated by Reduction of 1,2-Bis(bromomethyl)benzene with Zinc
    • Kise, N.; Mimura, R. Diastereoselective Cycloaddition of Chiral 1-Acryloyl-2-Imidazolidinone and o -Quinodimethane Generated by Reduction of 1,2-Bis(bromomethyl)benzene with Zinc Tetrahedron: Asymmetry 2007, 18, 988-993
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 988-993
    • Kise, N.1    Mimura, R.2
  • 198
    • 80053089739 scopus 로고    scopus 로고
    • Asymmetric Catalysis of Diels-Alder Reactions with in Situ Generated Heterocyclic ortho-Quinodimethanes
    • Liu, Y.; Nappi, M.; Arceo, E.; Vera, S.; Melchiorre, P. Asymmetric Catalysis of Diels-Alder Reactions with in Situ Generated Heterocyclic ortho-Quinodimethanes J. Am. Chem. Soc. 2011, 133, 15212-15218
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 15212-15218
    • Liu, Y.1    Nappi, M.2    Arceo, E.3    Vera, S.4    Melchiorre, P.5
  • 199
    • 84863229385 scopus 로고    scopus 로고
    • Multicatalytic Asymmetric Synthesis of Complex Tetrahydrocarbazoles via a Diels-Alder/Benzoin Reaction Sequence
    • Liu, Y.; Nappi, M.; Escudero-Adán, E. C.; Melchiorre, P. Multicatalytic Asymmetric Synthesis of Complex Tetrahydrocarbazoles via a Diels-Alder/Benzoin Reaction Sequence Org. Lett. 2012, 14, 1310-1313
    • (2012) Org. Lett. , vol.14 , pp. 1310-1313
    • Liu, Y.1    Nappi, M.2    Escudero-Adán, E.C.3    Melchiorre, P.4
  • 200
    • 84870955024 scopus 로고    scopus 로고
    • Asymmetric Diels-Alder Reaction of 2-Methyl-3-indolylmethanols via in Situ Generation of o -Quinodimethanes
    • Xiao, Y.-C.; Zhou, Q.-Q.; Dong, L.; Liu, T.-Y.; Chen, Y.-C. Asymmetric Diels-Alder Reaction of 2-Methyl-3-indolylmethanols via in Situ Generation of o -Quinodimethanes Org. Lett. 2012, 14, 5940-5943
    • (2012) Org. Lett. , vol.14 , pp. 5940-5943
    • Xiao, Y.-C.1    Zhou, Q.-Q.2    Dong, L.3    Liu, T.-Y.4    Chen, Y.-C.5
  • 201
    • 0032580467 scopus 로고    scopus 로고
    • Synthesis of Constrained α-Amino Acid Derivatives via Enyne Metathesis Reaction
    • Kotha, S.; Sreenivasachary, N.; Brahmachary, E. Synthesis of Constrained α-Amino Acid Derivatives via Enyne Metathesis Reaction Tetrahedron Lett. 1998, 39, 2805-2808
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2805-2808
    • Kotha, S.1    Sreenivasachary, N.2    Brahmachary, E.3
  • 202
    • 0035135210 scopus 로고    scopus 로고
    • Constrained Phenylalanine Derivatives by Enyne Metathesis and Diels-Alder Reaction
    • Kotha, S.; Sreenivasachary, N.; Brahmachary, E. Constrained Phenylalanine Derivatives by Enyne Metathesis and Diels-Alder Reaction Eur. J. Org. Chem. 2001, 787-792
    • (2001) Eur. J. Org. Chem. , pp. 787-792
    • Kotha, S.1    Sreenivasachary, N.2    Brahmachary, E.3
  • 203
    • 42449131742 scopus 로고    scopus 로고
    • The Schöllkopf Chiron and Transition Metal Mediated Reactions, A Powerful Combination for Stereoselective Construction of Cyclic α-Quaternary-α-Amino Acid Derivatives
    • references cited therein
    • Undheim, K. The Schöllkopf Chiron and Transition Metal Mediated Reactions, A Powerful Combination for Stereoselective Construction of Cyclic α-Quaternary-α-Amino Acid Derivatives Amino Acids 2008, 34, 357-402 and references cited therein
    • (2008) Amino Acids , vol.34 , pp. 357-402
    • Undheim, K.1
  • 204
    • 84908674593 scopus 로고    scopus 로고
    • Diversity-oriented Synthesis of Medicinally Important 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid (Tic) Derivatives and Higher Analogs
    • Kotha, S.; Deodhar, D.; Khedkar, P. Diversity-oriented Synthesis of Medicinally Important 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid (Tic) Derivatives and Higher Analogs Org. Biomol. Chem. 2014, 12, 9054-9091
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 9054-9091
    • Kotha, S.1    Deodhar, D.2    Khedkar, P.3
  • 205
    • 0035353817 scopus 로고    scopus 로고
    • Synthetic Approaches to Tetrahydroisoquinoline-3-carboxylic Acid Derivatives
    • Kotha, S.; Sreenivasachary, N. Synthetic Approaches to Tetrahydroisoquinoline-3-carboxylic Acid Derivatives J. Indian Inst. Sci. 2001, 81, 277-286
    • (2001) J. Indian Inst. Sci. , vol.81 , pp. 277-286
    • Kotha, S.1    Sreenivasachary, N.2
  • 206
    • 0034696697 scopus 로고    scopus 로고
    • A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives via Enyne Metathesis and the Diels-Alder Reaction
    • Kotha, S.; Sreenivasachary, N. A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives via Enyne Metathesis and the Diels-Alder Reaction Chem. Commun. 2000, 503-504
    • (2000) Chem. Commun. , pp. 503-504
    • Kotha, S.1    Sreenivasachary, N.2
  • 207
    • 0034843209 scopus 로고    scopus 로고
    • Synthesis of 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives by Cycloaddition Approaches
    • Kotha, S.; Sreenivasachary, N. Synthesis of 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives by Cycloaddition Approaches Eur. J. Org. Chem. 2001, 3375-3383
    • (2001) Eur. J. Org. Chem. , pp. 3375-3383
    • Kotha, S.1    Sreenivasachary, N.2
  • 208
    • 53249094132 scopus 로고    scopus 로고
    • Synthesis of a Conformationally Constrained Phenylalanine Derivative by a Strategic Combination of Ring-Closing Enyne Metathesis and Diels-Alder Reaction
    • Kotha, S.; Khedkar, P. Synthesis of a Conformationally Constrained Phenylalanine Derivative by a Strategic Combination of Ring-Closing Enyne Metathesis and Diels-Alder Reaction Synthesis 2008, 2925-2928
    • (2008) Synthesis , pp. 2925-2928
    • Kotha, S.1    Khedkar, P.2
  • 209
    • 79960983511 scopus 로고    scopus 로고
    • A Synergistic Approach to Polycyclics via a Strategic Utilization of Claisen Rearrangement and Olefin Metathesis
    • Kotha, S.; Krishna, N. G.; Halder, S.; Misra, S. A Synergistic Approach to Polycyclics via a Strategic Utilization of Claisen Rearrangement and Olefin Metathesis Org. Biomol. Chem. 2011, 9, 5597-5624
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 5597-5624
    • Kotha, S.1    Krishna, N.G.2    Halder, S.3    Misra, S.4
  • 210
    • 33750552076 scopus 로고    scopus 로고
    • Diversity-Oriented Approach to Biologically Relevant Molecular Frameworks Starting with β-Naphthol and Using the Claisen Rearrangement and Olefin Metathesis as Key Steps
    • Kotha, S.; Mandal, K.; Tiwari, A.; Mobin, S. M. Diversity-Oriented Approach to Biologically Relevant Molecular Frameworks Starting with β-Naphthol and Using the Claisen Rearrangement and Olefin Metathesis as Key Steps Chem. - Eur. J. 2006, 12, 8024-8038
    • (2006) Chem. - Eur. J. , vol.12 , pp. 8024-8038
    • Kotha, S.1    Mandal, K.2    Tiwari, A.3    Mobin, S.M.4
  • 212
    • 84906946518 scopus 로고    scopus 로고
    • Design and Synthesis of Angularly Annulated Spirocyclics via Enyne Metathesis and the Diels-Alder Reaction as Key Steps
    • Kotha, S.; Ali, R.; Tiwari, A. Design and Synthesis of Angularly Annulated Spirocyclics via Enyne Metathesis and the Diels-Alder Reaction as Key Steps Synthesis 2014, 2471-2480
    • (2014) Synthesis , pp. 2471-2480
    • Kotha, S.1    Ali, R.2    Tiwari, A.3
  • 213
    • 84908438740 scopus 로고    scopus 로고
    • Diversity-Oriented Approach to Carbocycles and Heterocycles through Ring Rearrangement Metathesis, Fischer Indole Cyclization, and Diels-Alder Reaction as Key Steps
    • Kotha, S.; Ravikumar, O. Diversity-Oriented Approach to Carbocycles and Heterocycles through Ring Rearrangement Metathesis, Fischer Indole Cyclization, and Diels-Alder Reaction as Key Steps Eur. J. Org. Chem. 2014, 5582-5590
    • (2014) Eur. J. Org. Chem. , pp. 5582-5590
    • Kotha, S.1    Ravikumar, O.2
  • 214
    • 84908446920 scopus 로고    scopus 로고
    • Design and Synthesis of Oxa-bowls via Diels-Alder Reaction and Ring-Rearrangement Metathesis as Key Steps
    • Kotha, S.; Ravikumar, O. Design and Synthesis of Oxa-bowls via Diels-Alder Reaction and Ring-Rearrangement Metathesis as Key Steps Tetrahedron Lett. 2014, 55, 5781-5784
    • (2014) Tetrahedron Lett. , vol.55 , pp. 5781-5784
    • Kotha, S.1    Ravikumar, O.2
  • 215
    • 33747197191 scopus 로고    scopus 로고
    • Synthesis of Oxepine-, Oxocine- and Azepine-Annulated Carbazole Derivatives by Combined Claisen Rearrangement and Diene/Enyne Metathesis
    • Chattopadhyay, S. K.; Roy, S. P.; Ghosh, D.; Biswas, G. Synthesis of Oxepine-, Oxocine- and Azepine-Annulated Carbazole Derivatives by Combined Claisen Rearrangement and Diene/Enyne Metathesis Tetrahedron Lett. 2006, 47, 6895-6898
    • (2006) Tetrahedron Lett. , vol.47 , pp. 6895-6898
    • Chattopadhyay, S.K.1    Roy, S.P.2    Ghosh, D.3    Biswas, G.4
  • 217
    • 53649100112 scopus 로고    scopus 로고
    • Design and Synthesis of 1-Benzazepine Derivatives by Strategic Utilization of Suzuki-Miyaura Cross-Coupling, Aza-Claisen Rearrangement and Ring-Closing Metathesis
    • Kotha, S.; Shah, V. R. Design and Synthesis of 1-Benzazepine Derivatives by Strategic Utilization of Suzuki-Miyaura Cross-Coupling, Aza-Claisen Rearrangement and Ring-Closing Metathesis Eur. J. Org. Chem. 2008, 1054-1064
    • (2008) Eur. J. Org. Chem. , pp. 1054-1064
    • Kotha, S.1    Shah, V.R.2
  • 219
    • 65649110353 scopus 로고    scopus 로고
    • Aza-Claisen Rearrangement
    • Hiersemann, M. Nubbemeyer, U. Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany
    • Nubbemeyer, U. Aza-Claisen Rearrangement. In The Claisen Rearrangement: Methods and Applications; Hiersemann, M.; Nubbemeyer, U., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2007; pp 461-523.
    • (2007) The Claisen Rearrangement: Methods and Applications , pp. 461-523
    • Nubbemeyer, U.1
  • 221
    • 84859239885 scopus 로고    scopus 로고
    • A Unified Strategy for the Syntheses of Angucyclinone Antibiotics: Total Syntheses of Tetrangulol, Kanglemycin M, X-14881-E, and Anhydrolandomycinone
    • Vanga, D. G.; Kaliappan, K. P. A Unified Strategy for the Syntheses of Angucyclinone Antibiotics: Total Syntheses of Tetrangulol, Kanglemycin M, X-14881-E, and Anhydrolandomycinone Eur. J. Org. Chem. 2012, 2250-2259
    • (2012) Eur. J. Org. Chem. , pp. 2250-2259
    • Vanga, D.G.1    Kaliappan, K.P.2
  • 222
    • 84868451154 scopus 로고    scopus 로고
    • Total Synthesis and Stereochemical Assignment of (-)-Zenkequinone B
    • Vanga, D. G.; Kaliappan, K. P. Total Synthesis and Stereochemical Assignment of (-)-Zenkequinone B Synlett 2012, 2931-2934
    • (2012) Synlett , pp. 2931-2934
    • Vanga, D.G.1    Kaliappan, K.P.2
  • 223
    • 84864069841 scopus 로고    scopus 로고
    • Discovery of a Multi-Bond Forming, Four-Step Tandem Process: Construction of Drug-Like Polycyclic Scaffolds
    • Grafton, M. W.; Farrugia, L. J.; Senn, H. M.; Sutherland, A. Discovery of a Multi-Bond Forming, Four-Step Tandem Process: Construction of Drug-Like Polycyclic Scaffolds Chem. Commun. 2012, 48, 7994-7996
    • (2012) Chem. Commun. , vol.48 , pp. 7994-7996
    • Grafton, M.W.1    Farrugia, L.J.2    Senn, H.M.3    Sutherland, A.4
  • 224
    • 0022376894 scopus 로고
    • A Stereorational Total Synthesis of (-)-Ptilocaulin
    • Walts, A. E.; Roush, W. R. A Stereorational Total Synthesis of (-)-Ptilocaulin Tetrahedron 1985, 41, 3463-3478
    • (1985) Tetrahedron , vol.41 , pp. 3463-3478
    • Walts, A.E.1    Roush, W.R.2
  • 226
    • 84880548994 scopus 로고    scopus 로고
    • Synthesis of Amino-Substituted Indanes and Tetralins via Consecutive Multibond-Forming Tandem Processes
    • Grafton, M. W.; Farrugia, L. J.; Sutherland, A. Synthesis of Amino-Substituted Indanes and Tetralins via Consecutive Multibond-Forming Tandem Processes J. Org. Chem. 2013, 78, 7199-7207
    • (2013) J. Org. Chem. , vol.78 , pp. 7199-7207
    • Grafton, M.W.1    Farrugia, L.J.2    Sutherland, A.3
  • 227
    • 77954557653 scopus 로고    scopus 로고
    • Construction of a Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway
    • Oh, S.; Jang, H. J.; Ko, S. K.; Ko, Y.; Park, S. B. Construction of a Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway J. Comb. Chem. 2010, 12, 548-558
    • (2010) J. Comb. Chem. , vol.12 , pp. 548-558
    • Oh, S.1    Jang, H.J.2    Ko, S.K.3    Ko, Y.4    Park, S.B.5
  • 228
    • 80052779364 scopus 로고    scopus 로고
    • Versatile Solid-Phase Synthesis of Chromenes Resembling Classical Cannabinoids
    • Kapeller, D. C.; Bräse, S. Versatile Solid-Phase Synthesis of Chromenes Resembling Classical Cannabinoids ACS Comb. Sci. 2011, 13, 554-561
    • (2011) ACS Comb. Sci. , vol.13 , pp. 554-561
    • Kapeller, D.C.1    Bräse, S.2
  • 229
    • 84863116367 scopus 로고    scopus 로고
    • Construction of Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway: Part II
    • Zhu, M.; Lim, B. J.; Koh, M.; Park, S. B. Construction of Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway: Part II ACS Comb. Sci. 2012, 14, 124-134
    • (2012) ACS Comb. Sci. , vol.14 , pp. 124-134
    • Zhu, M.1    Lim, B.J.2    Koh, M.3    Park, S.B.4
  • 230
    • 78651247094 scopus 로고    scopus 로고
    • Diversity Through a Branched Reaction Pathway: Generation of Multicyclic Scaffolds and Identification of Antimigratory Agents
    • Wang, Z.; Castellano, S.; Kinderman, S. S.; Argueta, C. E.; Beshir, A. B.; Fenteany, G.; Kwon, O. Diversity Through a Branched Reaction Pathway: Generation of Multicyclic Scaffolds and Identification of Antimigratory Agents Chem. - Eur. J. 2011, 17, 649-654
    • (2011) Chem. - Eur. J. , vol.17 , pp. 649-654
    • Wang, Z.1    Castellano, S.2    Kinderman, S.S.3    Argueta, C.E.4    Beshir, A.B.5    Fenteany, G.6    Kwon, O.7
  • 231
    • 79955568049 scopus 로고    scopus 로고
    • Diversity Through Phosphine Catalysis Identifies Octahydro-1,6-naphthyridin-4-ones as Activators of Endothelium-Driven Immunity
    • Cruz, D.; Wang, Z.; Kibbie, J.; Modlin, R.; Kwon, O. Diversity Through Phosphine Catalysis Identifies Octahydro-1,6-naphthyridin-4-ones as Activators of Endothelium-Driven Immunity Proc. Natl. Acad. Sci. U.S.A. 2011, 108, 6769-6774
    • (2011) Proc. Natl. Acad. Sci. U.S.A. , vol.108 , pp. 6769-6774
    • Cruz, D.1    Wang, Z.2    Kibbie, J.3    Modlin, R.4    Kwon, O.5
  • 233
    • 79952448533 scopus 로고    scopus 로고
    • A Rapid Assembly of Furo[3,4-b]- and Pyrrolo[3,4-b]carbazolones by Domino Wittig/Diels-Alder Reaction
    • Torney, P.; Patre, R.; Tilve, S. A Rapid Assembly of Furo[3,4-b]- and Pyrrolo[3,4-b]carbazolones by Domino Wittig/Diels-Alder Reaction Synlett 2011, 639-642
    • (2011) Synlett , pp. 639-642
    • Torney, P.1    Patre, R.2    Tilve, S.3
  • 234
    • 84880030658 scopus 로고    scopus 로고
    • An Efficient and Facile Synthesis of Iminoquinazolinedione Derivatives by Solid-State Diels-Alder Reaction under Catalyst-Free Conditions
    • Sarmah, M. M.; Bhuyan, D.; Prajapati, D. An Efficient and Facile Synthesis of Iminoquinazolinedione Derivatives by Solid-State Diels-Alder Reaction under Catalyst-Free Conditions Synlett 2013, 1667-1670
    • (2013) Synlett , pp. 1667-1670
    • Sarmah, M.M.1    Bhuyan, D.2    Prajapati, D.3
  • 235
    • 0028144422 scopus 로고
    • Exo Diastereoselective Diels-Alder Reactions of (R)-2-Phenyl-4-methylene-oxazolidin-5-one
    • Pyne, S. G.; Safaei-G, J.; Hockless, D. C. R.; Skelton, B. W.; Sobolev, A. N.; White, A. H. Exo Diastereoselective Diels-Alder Reactions of (R)-2-Phenyl-4-methylene-oxazolidin-5-one Tetrahedron 1994, 50, 941-956
    • (1994) Tetrahedron , vol.50 , pp. 941-956
    • Pyne, S.G.1    Safaei-G, J.2    Hockless, D.C.R.3    Skelton, B.W.4    Sobolev, A.N.5    White, A.H.6
  • 236
    • 2742584946 scopus 로고    scopus 로고
    • Synthesis of (+)-(2 S)-2-Aminobicyclo[2.2.2]octane-2-carboxylic Acid
    • Pyne, S. G.; Safaei-G, J. Synthesis of (+)-(2 S)-2-Aminobicyclo[2.2.2]octane-2-carboxylic Acid J. Chem. Res. (Part S) 1996, 160-161
    • (1996) J. Chem. Res. (Part S) , pp. 160-161
    • Pyne, S.G.1    Safaei-G, J.2
  • 237
    • 0001245684 scopus 로고    scopus 로고
    • The Use of 4-Hetaryliden- and 4-Aryliden-5(4 H)-oxazolones as Dienophiles. Appropriate Reagents for the Synthesis of Cyclic Analogues of Natural Amino Acids
    • Avenoza, A.; Busto, J. H.; Paris, M.; Peregrina, J. M.; Cativiela, C. The Use of 4-Hetaryliden- and 4-Aryliden-5(4 H)-oxazolones as Dienophiles. Appropriate Reagents for the Synthesis of Cyclic Analogues of Natural Amino Acids J. Heterocycl. Chem. 1997, 34, 1099-1110
    • (1997) J. Heterocycl. Chem. , vol.34 , pp. 1099-1110
    • Avenoza, A.1    Busto, J.H.2    Paris, M.3    Peregrina, J.M.4    Cativiela, C.5
  • 238
    • 0034685901 scopus 로고    scopus 로고
    • New Chiral Didehydroamino Acid Derivatives from a Cyclic Glycine Template with 3,6-Dihydro-2 H -1,4-oxazin-2-one Structure: Applications to the Asymmetric Synthesis of Nonproteinogenic α-Amino Acids
    • Chinchilla, R.; Falvello, L. R.; Galindo, N.; Nájera, C. New Chiral Didehydroamino Acid Derivatives from a Cyclic Glycine Template with 3,6-Dihydro-2 H -1,4-oxazin-2-one Structure: Applications to the Asymmetric Synthesis of Nonproteinogenic α-Amino Acids J. Org. Chem. 2000, 65, 3034-3041
    • (2000) J. Org. Chem. , vol.65 , pp. 3034-3041
    • Chinchilla, R.1    Falvello, L.R.2    Galindo, N.3    Nájera, C.4
  • 239
    • 79957777291 scopus 로고    scopus 로고
    • Serendipitous and Acid Catalyzed Synthesis of Spirolactones
    • Kotha, S.; Dipak, M. K.; Mobin, S. M. Serendipitous and Acid Catalyzed Synthesis of Spirolactones Tetrahedron 2011, 67, 4616-4619
    • (2011) Tetrahedron , vol.67 , pp. 4616-4619
    • Kotha, S.1    Dipak, M.K.2    Mobin, S.M.3
  • 240
    • 0000979441 scopus 로고    scopus 로고
    • Synthesis of Polyquinane Natural Products: An Update
    • Mehta, G.; Srikrishna, A. Synthesis of Polyquinane Natural Products: An Update Chem. Rev. 1997, 97, 671-720
    • (1997) Chem. Rev. , vol.97 , pp. 671-720
    • Mehta, G.1    Srikrishna, A.2
  • 242
    • 0000987357 scopus 로고
    • Polycyclic Cage Compounds: Reagents, Substrates, and Materials for the 21st Century
    • Marchand, A. P. Polycyclic Cage Compounds: Reagents, Substrates, and Materials for the 21st Century Aldrichim. Acta 1995, 28, 95-104
    • (1995) Aldrichim. Acta , vol.28 , pp. 95-104
    • Marchand, A.P.1
  • 244
    • 84877712527 scopus 로고    scopus 로고
    • Recent Developments in the Retro-Diels-Alder Reaction
    • Kotha, S.; Banerjee, S. Recent Developments in the Retro-Diels-Alder Reaction RSC Adv. 2013, 3, 7642-7666
    • (2013) RSC Adv. , vol.3 , pp. 7642-7666
    • Kotha, S.1    Banerjee, S.2
  • 245
    • 33646745355 scopus 로고    scopus 로고
    • Retro Diels-Alder Reaction under Mild Conditions: Experimental and Theoretical Studies
    • Kotha, S.; Banerjee, S.; Patil, M. P.; Sunoj, R. B. Retro Diels-Alder Reaction under Mild Conditions: Experimental and Theoretical Studies Org. Biomol. Chem. 2006, 4, 1854-1856
    • (2006) Org. Biomol. Chem. , vol.4 , pp. 1854-1856
    • Kotha, S.1    Banerjee, S.2    Patil, M.P.3    Sunoj, R.B.4
  • 246
    • 84911925642 scopus 로고    scopus 로고
    • Correlation between Carbon-Carbon Bond Length and the Ease of retro Diels-Alder Reaction
    • Kotha, S.; Banerjee, S.; Shaikh, M. Correlation between Carbon-Carbon Bond Length and the Ease of retro Diels-Alder Reaction J. Chem. Sci. 2014, 126, 1369-1371
    • (2014) J. Chem. Sci. , vol.126 , pp. 1369-1371
    • Kotha, S.1    Banerjee, S.2    Shaikh, M.3
  • 247
    • 84863109258 scopus 로고    scopus 로고
    • A Green Synthetic Route to Antimalarial and Antibacterial Agent CJ-15,801 and its Isomer Cis-CJ-15,801
    • Kashinath, K.; Swaroop, P. S.; Srinivasa Reddy, D. A Green Synthetic Route to Antimalarial and Antibacterial Agent CJ-15,801 and its Isomer Cis-CJ-15,801 RSC Adv. 2012, 2, 3596-3598
    • (2012) RSC Adv. , vol.2 , pp. 3596-3598
    • Kashinath, K.1    Swaroop, P.S.2    Srinivasa Reddy, D.3
  • 248
    • 0742321841 scopus 로고    scopus 로고
    • Copper-Mediated Synthesis of N -Acyl Vinylogous Carbamic Acids and Derivatives: Synthesis of the Antibiotic CJ-15,801
    • Han, C.; Shen, R.; Su, S.; Porco, J. A., Jr. Copper-Mediated Synthesis of N -Acyl Vinylogous Carbamic Acids and Derivatives: Synthesis of the Antibiotic CJ-15,801 Org. Lett. 2004, 6, 27-30
    • (2004) Org. Lett. , vol.6 , pp. 27-30
    • Han, C.1    Shen, R.2    Su, S.3    Porco, J.A.4
  • 249
    • 33846252976 scopus 로고    scopus 로고
    • Design and Synthesis of Spirocyclics via the Diels-Alder Reaction and Ring-Opening Cross-Metathesis as Key Steps
    • Kotha, S.; Deb, A. C.; Chattopadhyay, S. Design and Synthesis of Spirocyclics via the Diels-Alder Reaction and Ring-Opening Cross-Metathesis as Key Steps Lett. Org. Chem. 2006, 3, 128-134
    • (2006) Lett. Org. Chem. , vol.3 , pp. 128-134
    • Kotha, S.1    Deb, A.C.2    Chattopadhyay, S.3
  • 250
    • 33744792315 scopus 로고    scopus 로고
    • Design and Synthesis of Novel Propellanes by Using Claisen Rearrangement and Ring-Closing Metathesis as the Key Steps
    • Kotha, S.; Dipak, M. K. Design and Synthesis of Novel Propellanes by Using Claisen Rearrangement and Ring-Closing Metathesis as the Key Steps Chem. - Eur. J. 2006, 12, 4446-4450
    • (2006) Chem. - Eur. J. , vol.12 , pp. 4446-4450
    • Kotha, S.1    Dipak, M.K.2
  • 252
    • 84920092327 scopus 로고    scopus 로고
    • Design and Synthesis of Novel Bis-Annulated Caged Polycycles via Ring-Closing Metathesis: Pushpakenediol
    • Kotha, S.; Dipak, M. K. Design and Synthesis of Novel Bis-Annulated Caged Polycycles via Ring-Closing Metathesis: Pushpakenediol Beilstein J. Org. Chem. 2014, 10, 2664-2670
    • (2014) Beilstein J. Org. Chem. , vol.10 , pp. 2664-2670
    • Kotha, S.1    Dipak, M.K.2
  • 253
    • 79953078618 scopus 로고    scopus 로고
    • Synthesis and Reactions of a New 1,1-Disubstituted Cyclopentadiene
    • Camps, P.; Gómez, T. Synthesis and Reactions of a New 1,1-Disubstituted Cyclopentadiene ARKIVOC 2011, iii) 128-139
    • (2011) ARKIVOC , Issue.3 , pp. 128-139
    • Camps, P.1    Gómez, T.2
  • 254
    • 82955237481 scopus 로고    scopus 로고
    • Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes
    • Dejmek, M.; Hřebabecký, H.; Šála, M.; Dračínský, M.; Nencka, R. Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes Synthesis 2011, 4077-4083
    • (2011) Synthesis , pp. 4077-4083
    • Dejmek, M.1    Hřebabecký, H.2    Šála, M.3    Dračínský, M.4    Nencka, R.5
  • 255
    • 29844455070 scopus 로고    scopus 로고
    • Small-Molecule Diversity Using a Skeletal Transformation Strategy
    • Kumar, N.; Kiuchi, M.; Tallarico, J. A.; Schreiber, S. L. Small-Molecule Diversity Using a Skeletal Transformation Strategy Org. Lett. 2005, 7, 2535-2538
    • (2005) Org. Lett. , vol.7 , pp. 2535-2538
    • Kumar, N.1    Kiuchi, M.2    Tallarico, J.A.3    Schreiber, S.L.4
  • 256
    • 84978042983 scopus 로고
    • Synthesen in der Hydroaromatischen Reihe. VIII. Mitteilung: Dien-Synthesen des Anthracens. Anthracen-Formel
    • Diels, O.; Alder, K. Synthesen in der Hydroaromatischen Reihe. VIII. Mitteilung: Dien-Synthesen des Anthracens. Anthracen-Formel Justus Liebigs Ann.Chem. 1931, 486, 191-202
    • (1931) Justus Liebigs Ann.Chem. , vol.486 , pp. 191-202
    • Diels, O.1    Alder, K.2
  • 257
    • 85178397706 scopus 로고
    • Zur Kenntnis Mehrkerniger Aromatischer Kohlenwasserstoffe und ihrer Abkömmlinge, XI. Mitteil.: Über die Konstitution des Anthracens, II.: Bemerkungen zu einer Arbeit von Otto Diels und Kurt Alder
    • Clar, E. Zur Kenntnis Mehrkerniger Aromatischer Kohlenwasserstoffe und ihrer Abkömmlinge, XI. Mitteil.: Über die Konstitution des Anthracens, II.: Bemerkungen zu einer Arbeit von Otto Diels und Kurt Alder Ber. Dtsch. Chem. Ges. A/B 1931, 64, 2194-2200
    • (1931) Ber. Dtsch. Chem. Ges. A/B , vol.64 , pp. 2194-2200
    • Clar, E.1
  • 258
    • 0142196137 scopus 로고    scopus 로고
    • Diels-Alder Reactions of Anthracene, 9-Substituted Anthracenes and 9,10-Disubstituted Anthracenes
    • Atherton, J. C. C.; Jones, S. Diels-Alder Reactions of Anthracene, 9-Substituted Anthracenes and 9,10-Disubstituted Anthracenes Tetrahedron 2003, 59, 9039-9057
    • (2003) Tetrahedron , vol.59 , pp. 9039-9057
    • Atherton, J.C.C.1    Jones, S.2
  • 259
    • 0036868391 scopus 로고    scopus 로고
    • Synthesis of Highly Constrained Unusual α-Amino Acid Derivative by the Diels-Alder Approach
    • Kotha, S.; Ghosh, A. K.; Behera, M. Synthesis of Highly Constrained Unusual α-Amino Acid Derivative by the Diels-Alder Approach Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2002, 41B, 2330-2332
    • (2002) Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. , vol.41 , pp. 2330-2332
    • Kotha, S.1    Ghosh, A.K.2    Behera, M.3
  • 267
    • 15944420883 scopus 로고    scopus 로고
    • Highly Regioselective Diels-Alder Reactions of 9-Substituted Anthracenes and 2-Acetamidoacrylate: Synthesis of Conformationally Constrained α-Amino Acids
    • Yang, B. V.; Doweyko, L. M. Highly Regioselective Diels-Alder Reactions of 9-Substituted Anthracenes and 2-Acetamidoacrylate: Synthesis of Conformationally Constrained α-Amino Acids Tetrahedron Lett. 2005, 46, 2857-2860
    • (2005) Tetrahedron Lett. , vol.46 , pp. 2857-2860
    • Yang, B.V.1    Doweyko, L.M.2
  • 269
    • 84927923697 scopus 로고    scopus 로고
    • Synthesis of Conformationally Constrained α-Amino Acid Derivatives Containing Bicyclo[2.2.2]octane Unit via the Diels-Alder Reaction and the Suzuki-Miyaura Cross-Coupling as Key Steps
    • Kotha, S.; Meshram, M.; Muthusamy, G. Synthesis of Conformationally Constrained α-Amino Acid Derivatives Containing Bicyclo[2.2.2]octane Unit via the Diels-Alder Reaction and the Suzuki-Miyaura Cross-Coupling as Key Steps Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2015, 54B, 505-513
    • (2015) Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. , vol.54 , pp. 505-513
    • Kotha, S.1    Meshram, M.2    Muthusamy, G.3
  • 270
    • 84923283740 scopus 로고    scopus 로고
    • Design and Synthesis of Conformationally Constrained Bicyclo[2.2.2]octane-Based Unusual α-Amino Acid Derivatives via the Diels-Alder Reaction
    • Kotha, S.; Meshram, M. Design and Synthesis of Conformationally Constrained Bicyclo[2.2.2]octane-Based Unusual α-Amino Acid Derivatives via the Diels-Alder Reaction Heterocycles 2015, 90, 357-371
    • (2015) Heterocycles , vol.90 , pp. 357-371
    • Kotha, S.1    Meshram, M.2
  • 271
    • 84891333201 scopus 로고    scopus 로고
    • Functionalization of Anthracene by Strategic Utilization of the Diels-Alder Reaction and the Ring-Closing Metathesis
    • Kotha, S.; Meshram, M. Functionalization of Anthracene by Strategic Utilization of the Diels-Alder Reaction and the Ring-Closing Metathesis J. Indian Chem. Soc. 2013, 90, 1789-1794
    • (2013) J. Indian Chem. Soc. , vol.90 , pp. 1789-1794
    • Kotha, S.1    Meshram, M.2
  • 272
    • 84887075869 scopus 로고    scopus 로고
    • Diels-Alder Reactions of 9-Ferrocenyl- and 9,10-Diferrocenylanthracene: Steric Control of 9,10-versus 1,4-Cycloaddition
    • Nikitin, K.; Müller-Bunz, H.; McGlinchey, M. J. Diels-Alder Reactions of 9-Ferrocenyl- and 9,10-Diferrocenylanthracene: Steric Control of 9,10-versus 1,4-Cycloaddition Organometallics 2013, 32, 6118-6129
    • (2013) Organometallics , vol.32 , pp. 6118-6129
    • Nikitin, K.1    Müller-Bunz, H.2    McGlinchey, M.J.3
  • 273
    • 84865517099 scopus 로고    scopus 로고
    • Using Light and a Molecular Switch to 'Lock' and 'Unlock' the Diels-Alder Reaction
    • Erno, Z.; Asadirad, A. M.; Lemieux, V.; Branda, N. R. Using Light and a Molecular Switch to 'Lock' and 'Unlock' the Diels-Alder Reaction Org. Biomol. Chem. 2012, 10, 2787-2792
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 2787-2792
    • Erno, Z.1    Asadirad, A.M.2    Lemieux, V.3    Branda, N.R.4
  • 274
    • 84884533615 scopus 로고    scopus 로고
    • Towards Molecular Ribbons of Corannulene
    • Furrer, F.; Linden, A.; Stuparu, M. C. Towards Molecular Ribbons of Corannulene Chem. - Eur. J. 2013, 19, 13199-13206
    • (2013) Chem. - Eur. J. , vol.19 , pp. 13199-13206
    • Furrer, F.1    Linden, A.2    Stuparu, M.C.3
  • 275
    • 70349787847 scopus 로고    scopus 로고
    • In Situ Enamine Activation in Aqueous Salt Solutions: Highly Efficient Asymmetric Organocatalytic Diels-Alder Reaction of Cyclohexenones with Nitroolefins
    • Xu, D.-Q.; Xia, A.-B.; Luo, S.-P.; Tang, J.; Zhang, S.; Jiang, J.-R.; Xu, Z.-Y. In Situ Enamine Activation in Aqueous Salt Solutions: Highly Efficient Asymmetric Organocatalytic Diels-Alder Reaction of Cyclohexenones with Nitroolefins Angew. Chem., Int. Ed. 2009, 48, 3821-3824
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 3821-3824
    • Xu, D.-Q.1    Xia, A.-B.2    Luo, S.-P.3    Tang, J.4    Zhang, S.5    Jiang, J.-R.6    Xu, Z.-Y.7
  • 276
    • 84864259502 scopus 로고    scopus 로고
    • Diels-Alder Cycloaddition of Acetylene Gas to a Polycyclic Aromatic Hydrocarbon Bay Region
    • Fort, E. H.; Jeffreys, M. S.; Scott, L. T. Diels-Alder Cycloaddition of Acetylene Gas to a Polycyclic Aromatic Hydrocarbon Bay Region Chem. Commun. 2012, 48, 8102-8104
    • (2012) Chem. Commun. , vol.48 , pp. 8102-8104
    • Fort, E.H.1    Jeffreys, M.S.2    Scott, L.T.3
  • 277
    • 84883471350 scopus 로고    scopus 로고
    • An Electron Rich Porous Extended Framework as a Heterogeneous Catalyst for Diels-Alder Reactions
    • Gole, B.; Bar, A. K.; Mallick, A.; Banerjee, R.; Mukherjee, P. S. An Electron Rich Porous Extended Framework as a Heterogeneous Catalyst for Diels-Alder Reactions Chem. Commun. 2013, 49, 7439-7441
    • (2013) Chem. Commun. , vol.49 , pp. 7439-7441
    • Gole, B.1    Bar, A.K.2    Mallick, A.3    Banerjee, R.4    Mukherjee, P.S.5
  • 278
    • 84861227809 scopus 로고    scopus 로고
    • Synthesis of Tetrahydroanthracen-9-ones by the Domino Aldol Condensation/Diels-Alder Cycloaddition
    • Chang, M.-Y.; Wu, M.-H. Synthesis of Tetrahydroanthracen-9-ones by the Domino Aldol Condensation/Diels-Alder Cycloaddition Tetrahedron Lett. 2012, 53, 3173-3177
    • (2012) Tetrahedron Lett. , vol.53 , pp. 3173-3177
    • Chang, M.-Y.1    Wu, M.-H.2
  • 279
    • 84881242218 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Synthesis of Tetracyclic Pyridocarbazole Derivatives by Using a Diels-Alder/aza-Michael/Aldol Condensation Domino Reaction
    • Enders, D.; Joie, C.; Deckers, K. Organocatalytic Asymmetric Synthesis of Tetracyclic Pyridocarbazole Derivatives by Using a Diels-Alder/aza-Michael/Aldol Condensation Domino Reaction Chem. - Eur. J. 2013, 19, 10818-10821
    • (2013) Chem. - Eur. J. , vol.19 , pp. 10818-10821
    • Enders, D.1    Joie, C.2    Deckers, K.3
  • 280
    • 84894089672 scopus 로고    scopus 로고
    • Efficient One-Pot Synthesis of Novel and Diverse Tetrahydroquinolines Bearing Pyranopyrazoles Using Organocatalyzed Domino Knoevenagel/Hetero Diels-Alder Reactions
    • Pandit, R. P.; Lee, Y. R. Efficient One-Pot Synthesis of Novel and Diverse Tetrahydroquinolines Bearing Pyranopyrazoles Using Organocatalyzed Domino Knoevenagel/Hetero Diels-Alder Reactions Mol. Divers. 2014, 18, 39-50
    • (2014) Mol. Divers. , vol.18 , pp. 39-50
    • Pandit, R.P.1    Lee, Y.R.2
  • 281
    • 84862016521 scopus 로고    scopus 로고
    • Synthesis of Heterocycles by Domino-Knoevenagel/Hetero-Diels-Alder Reactions
    • Majumdar, K. C.; Taher, A.; Nandi, R. K. Synthesis of Heterocycles by Domino-Knoevenagel/Hetero-Diels-Alder Reactions Tetrahedron 2012, 68, 5693-5718
    • (2012) Tetrahedron , vol.68 , pp. 5693-5718
    • Majumdar, K.C.1    Taher, A.2    Nandi, R.K.3
  • 283
    • 34547661989 scopus 로고    scopus 로고
    • Sequential Diels-Alder and Cobalt Octacarbonyl Catalyzed Pauson-Khand Reactions in the Formation of Polycyclic Enones
    • Choi, S. Y.; Lee, S. I.; Park, K. H.; Chung, Y. K. Sequential Diels-Alder and Cobalt Octacarbonyl Catalyzed Pauson-Khand Reactions in the Formation of Polycyclic Enones Synlett 2007, 1857-1862
    • (2007) Synlett , pp. 1857-1862
    • Choi, S.Y.1    Lee, S.I.2    Park, K.H.3    Chung, Y.K.4
  • 284
    • 69249237012 scopus 로고    scopus 로고
    • Synthesis of Substituted Fused Pyridines, Pyrazines and Pyrimidines by Sequential Ugi/Inverse Electron Demand Diels-Alder Transformations
    • Akritopoulou-Zanze, I.; Wang, Y.; Zhao, H.; Djuric, S. W. Synthesis of Substituted Fused Pyridines, Pyrazines and Pyrimidines by Sequential Ugi/Inverse Electron Demand Diels-Alder Transformations Tetrahedron Lett. 2009, 50, 5773-5776
    • (2009) Tetrahedron Lett. , vol.50 , pp. 5773-5776
    • Akritopoulou-Zanze, I.1    Wang, Y.2    Zhao, H.3    Djuric, S.W.4
  • 285
    • 78449248941 scopus 로고    scopus 로고
    • Platinum(II) Chloride-Catalyzed Stereoselective Domino Enyne Isomerization/Diels-Alder Reaction
    • Schelwies, M.; Farwick, A.; Rominger, F.; Helmchen, G. Platinum(II) Chloride-Catalyzed Stereoselective Domino Enyne Isomerization/Diels-Alder Reaction J. Org. Chem. 2010, 75, 7917-7919
    • (2010) J. Org. Chem. , vol.75 , pp. 7917-7919
    • Schelwies, M.1    Farwick, A.2    Rominger, F.3    Helmchen, G.4
  • 286
    • 84897547945 scopus 로고    scopus 로고
    • Intramolecular Diels-Alder Reaction as a Key Step in Tandem or Sequential Processes: A Versatile Tool for the Synthesis of Fused and Bridged Bicyclic or Polycyclic Compounds
    • Parvatkar, P. T.; Kadamb, H. K.; Tilve, S. G. Intramolecular Diels-Alder Reaction as a Key Step in Tandem or Sequential Processes: A Versatile Tool for the Synthesis of Fused and Bridged Bicyclic or Polycyclic Compounds Tetrahedron 2014, 70, 2857-2888
    • (2014) Tetrahedron , vol.70 , pp. 2857-2888
    • Parvatkar, P.T.1    Kadamb, H.K.2    Tilve, S.G.3
  • 287
    • 84887530181 scopus 로고    scopus 로고
    • [3]Dendralene Synthesis: Rhodium(III)-Catalyzed Alkenyl C-H Activation and Coupling Reaction with Allenyl Carbinol Carbonate
    • Wang, H.; Beiring, B.; Yu, D.-G.; Collins, K. D.; Glorius, F. [3]Dendralene Synthesis: Rhodium(III)-Catalyzed Alkenyl C-H Activation and Coupling Reaction with Allenyl Carbinol Carbonate Angew. Chem., Int. Ed. 2013, 52, 12430-12434
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 12430-12434
    • Wang, H.1    Beiring, B.2    Yu, D.-G.3    Collins, K.D.4    Glorius, F.5
  • 288
    • 84896767011 scopus 로고    scopus 로고
    • Rh(III)-Catalyzed C-H Activation with Allenes to Synthesize Conjugated Olefins
    • Gong, T.-J.; Su, W.; Liu, Z.-J.; Cheng, W.-M.; Xiao, B.; Fu, Y. Rh(III)-Catalyzed C-H Activation with Allenes to Synthesize Conjugated Olefins Org. Lett. 2014, 16, 330-333
    • (2014) Org. Lett. , vol.16 , pp. 330-333
    • Gong, T.-J.1    Su, W.2    Liu, Z.-J.3    Cheng, W.-M.4    Xiao, B.5    Fu, Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.