메뉴 건너뛰기




Volumn 5, Issue , 2014, Pages

Diversity-oriented synthesis of Lycopodium alkaloids inspired by the hidden functional group pairing pattern

Author keywords

[No Author keywords available]

Indexed keywords

8ALPHA HYDROXYFAWCETTIMINE; ALKALOID; FUNCTIONAL GROUP; LYCOPOSERRAMINE U; SERRATEZOMINE A; SERRATININE; UNCLASSIFIED DRUG; BIOLOGICAL PRODUCT; BIOMIMETIC MATERIAL; FUSED HETEROCYCLIC RINGS; INDOLIZINE DERIVATIVE;

EID: 84905489992     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms5614     Document Type: Article
Times cited : (52)

References (58)
  • 1
    • 39149137869 scopus 로고    scopus 로고
    • Plant-derived compounds in clinical trials
    • Saklani, A. & Kutty, S. K. Plant-derived compounds in clinical trials. Drug Discov. Today 13, 161-171 (2008
    • (2008) Drug Discov. Today , vol.13 , pp. 161-171
    • Saklani, A.1    Kutty, S.K.2
  • 3
    • 84863825873 scopus 로고    scopus 로고
    • Charting navigating, and populating natural product chemical space for drug discovery
    • Lachance, H., Wetzel, S., Kumar, K. & Waldmann, H. Charting, navigating, and populating natural product chemical space for drug discovery. J. Med. Chem. 55, 5989-6001 (2012
    • (2012) J. Med. Chem. , vol.55 , pp. 5989-6001
    • Lachance, H.1    Wetzel, S.2    Kumar, K.3    Waldmann, H.4
  • 5
    • 0001278411 scopus 로고
    • Total syntheses of azafluoranthene alkaloids: Rufescine and imeluteine
    • Boger, D. L. & Brotherton, C. E. Total syntheses of azafluoranthene alkaloids: Rufescine and imeluteine. J. Org. Chem. 49, 4050-4055 (1984
    • (1984) J. Org. Chem. , vol.49 , pp. 4050-4055
    • Boger, D.L.1    Brotherton, C.E.2
  • 6
    • 79960407415 scopus 로고    scopus 로고
    • Collective synthesis of natural products by means of organocascade catalysis
    • Jones, S. B., Simmons, B., Mastracchio, A. & MacMillan, D. W. C. Collective synthesis of natural products by means of organocascade catalysis. Nature 475, 183-188 (2011
    • (2011) Nature , vol.475 , pp. 183-188
    • Jones, S.B.1    Simmons, B.2    Mastracchio, A.3    Macmillan, D.W.C.4
  • 7
    • 84889669302 scopus 로고    scopus 로고
    • Divergent total synthesis of indoxamycins A,C, and F
    • He, C., Zhu, C., Dai, Z., Tseng, C.-C. & Ding, H. Divergent total synthesis of indoxamycins A, C, and F. Angew. Chem. Int. Ed. 52, 13256-13260 (2013
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 13256-13260
    • He, C.1    Zhu, C.2    Dai, Z.3    Tseng, C.-C.4    Ding, H.5
  • 8
    • 84896844137 scopus 로고    scopus 로고
    • Total syntheses of (-)-kopsifoline D and (-)-deoxoapodine: Divergent total synthesis via late-stage key strategic bond formation
    • Lee, K. & Boger, D. L. Total syntheses of (-)-kopsifoline D and (-)-deoxoapodine: Divergent total synthesis via late-stage key strategic bond formation. J. Am. Chem. Soc. 136, 3312-3317 (2014
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 3312-3317
    • Lee, K.1    Boger, D.L.2
  • 9
    • 84879074474 scopus 로고    scopus 로고
    • Simultaneous structure-activity studies and arming of natural products by C-H amination reveal cellular targets of eupalmerin acetate
    • Li, J. et al. Simultaneous structure-activity studies and arming of natural products by C-H amination reveal cellular targets of eupalmerin acetate. Nat. Chem. 5, 510-517 (2013
    • (2013) Nat. Chem. , vol.5 , pp. 510-517
    • Li, J.1
  • 11
    • 82055161640 scopus 로고    scopus 로고
    • Remodelling of the natural product fumagillol employing a reaction discovery approach
    • Balthaser, B. R., Maloney, M. C., Beeler, A. B., Porco, J. A. & Snyder, J. K. Remodelling of the natural product fumagillol employing a reaction discovery approach. Nat. Chem. 3, 969-973 (2011
    • (2011) Nat. Chem. , vol.3 , pp. 969-973
    • Balthaser, B.R.1    Maloney, M.C.2    Beeler, A.B.3    Porco, J.A.4    Snyder, J.K.5
  • 12
    • 84875466221 scopus 로고    scopus 로고
    • A ring-distortion strategy to construct stereochemically complex and structurally diverse compounds from natural products
    • Huigens, III R. W. et al. A ring-distortion strategy to construct stereochemically complex and structurally diverse compounds from natural products. Nat. Chem. 5, 195-202 (2013
    • (2013) Nat. Chem. , vol.5 , pp. 195-202
    • Huigens III, R.W.1
  • 13
    • 84890955037 scopus 로고    scopus 로고
    • Synthesis of complex and diverse compounds through ring distortion of abietic acid
    • Rafferty, R. J., Hicklin, R. W., Maloof, K. A. & Hergenrother, P. J. Synthesis of complex and diverse compounds through ring distortion of abietic acid. Angew. Chem. Int. Ed. 53, 220-224 (2014
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 220-224
    • Rafferty, R.J.1    Hicklin, R.W.2    Maloof, K.A.3    Hergenrother, P.J.4
  • 14
    • 84884830343 scopus 로고    scopus 로고
    • Component-based syntheses of trioxacarcin A DC-45-A1 and structural analogues
    • Magauer, T., Smaltz, D. J. & Myers, A. G. Component-based syntheses of trioxacarcin A, DC-45-A1 and structural analogues. Nat. Chem. 5, 886-893 (2013
    • (2013) Nat. Chem. , vol.5 , pp. 886-893
    • Magauer, T.1    Smaltz, D.J.2    Myers, A.G.3
  • 15
    • 84883661366 scopus 로고    scopus 로고
    • Synthesis of (±)-actinophyllic acid and analogues: Applications of cascade reactions and diverted total synthesis
    • Granger, B. A. et al. Synthesis of (±)-actinophyllic acid and analogues: Applications of cascade reactions and diverted total synthesis. J. Am. Chem. Soc. 135, 12984-12986 (2013
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 12984-12986
    • Granger, B.A.1
  • 16
    • 58849128316 scopus 로고    scopus 로고
    • Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach
    • Richter, J. M. et al. Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach. J. Am. Chem. Soc. 130, 17938-17954 (2008
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 17938-17954
    • Richter, J.M.1
  • 17
    • 84861510526 scopus 로고    scopus 로고
    • Diversity-oriented synthesis of diverse polycyclic scaffolds inspired by the logic of sesquiterpene lactones biosynthesis
    • Valot, G. et al. Diversity-oriented synthesis of diverse polycyclic scaffolds inspired by the logic of sesquiterpene lactones biosynthesis. Angew. Chem. Int. Ed. 51, 5391-5394 (2012
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5391-5394
    • Valot, G.1
  • 18
    • 84868525454 scopus 로고    scopus 로고
    • Scalable, enantioselective synthesis of germacrenes and related sesquiterpenes inspired by terpene cyclase phase logic
    • Foo, K. et al. Scalable, enantioselective synthesis of germacrenes and related sesquiterpenes inspired by terpene cyclase phase logic. Angew. Chem. Int. Ed. 51, 11491-11495 (2012
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 11491-11495
    • Foo, K.1
  • 19
    • 84890895066 scopus 로고    scopus 로고
    • Biogenetically inspired synthesis and skeletal diversification of indole alkaloids
    • Mizoguchi, H., Oikawa, H. & Oguri, H. Biogenetically inspired synthesis and skeletal diversification of indole alkaloids. Nat. Chem. 6, 57-64 (2014
    • (2014) Nat. Chem. , vol.6 , pp. 57-64
    • Mizoguchi, H.1    Oikawa, H.2    Oguri, H.3
  • 20
    • 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. 1, 3867-3870 (2003
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 3867-3870
    • Spring, D.R.1
  • 21
    • 3042799070 scopus 로고    scopus 로고
    • A planning strategy for diversity-oriented synthesis
    • DOI 10.1002/anie.200300626
    • Burke, M. D. & Schreiber, S. L. A planning strategy for diversity-oriented synthesis. Angew. Chem. Int. Ed. 43, 46-58 (2004 (Pubitemid 38063470)
    • (2004) Angewandte Chemie - International Edition , vol.43 , Issue.1 , pp. 46-58
    • Burke, M.D.1    Schreiber, S.L.2
  • 22
    • 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. 41, 4444-4456 (2012
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 4444-4456
    • O'Connor, C.J.1    Beckmann, H.S.G.2    Spring, D.R.3
  • 23
    • 37549020046 scopus 로고    scopus 로고
    • Towards the optimal screening collection: A synthesis strategy
    • Nielsen, T. E. & Schreiber, S. L. Towards the optimal screening collection: A synthesis strategy. Angew. Chem. Int. Ed. 47, 48-56 (2008
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 48-56
    • Nielsen, T.E.1    Schreiber, S.L.2
  • 24
    • 34250673184 scopus 로고    scopus 로고
    • An approach to skeletal diversity using functional group pairing of multifunctional scaffolds
    • Comer, E., Rohan, E., Deng, L. & Porco, J. A. An approach to skeletal diversity using functional group pairing of multifunctional scaffolds. Org. Lett. 9, 2123-2126 (2007
    • (2007) Org. Lett. , vol.9 , pp. 2123-2126
    • Comer, E.1    Rohan, E.2    Deng, L.3    Porco, J.A.4
  • 25
    • 82255170673 scopus 로고    scopus 로고
    • A design strategy for drug-like polyheterocycles with privileged substructures for discovery of specific small-molecule modulators
    • Oh, S. & Park, S. B. A design strategy for drug-like polyheterocycles with privileged substructures for discovery of specific small-molecule modulators. Chem. Commun. 47, 12754-12761 (2011
    • (2011) Chem. Commun. , vol.47 , pp. 12754-12761
    • Oh, S.1    Park, S.B.2
  • 26
    • 84887947768 scopus 로고    scopus 로고
    • Privileged substructure-based diversityoriented synthesis pathway for diverse pyrimidine-embedded polyheterocycles
    • Kim, H., Tung, T. T. & Park, S. B. Privileged substructure-based diversityoriented synthesis pathway for diverse pyrimidine-embedded polyheterocycles. Org. Lett. 15, 5814-5817 (2013
    • (2013) Org. Lett. , vol.15 , pp. 5814-5817
    • Kim, H.1    Tung, T.T.2    Park, S.B.3
  • 27
    • 58149346448 scopus 로고    scopus 로고
    • Synthesis of natural-product-like molecules with over eighty distinct scaffolds
    • Morton, D., Leach, S., Cordier, C., Warriner, S. & Nelson, A. Synthesis of natural-product-like molecules with over eighty distinct scaffolds. Angew. Chem. Int. Ed. 48, 104-109 (2009
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 104-109
    • Morton, D.1    Leach, S.2    Cordier, C.3    Warriner, S.4    Nelson, A.5
  • 28
    • 81355139618 scopus 로고    scopus 로고
    • Synthesis of natural-product-like scaffolds in unprecedented efficiency via a 12-fold branching pathway
    • Robbins, D. et al. Synthesis of natural-product-like scaffolds in unprecedented efficiency via a 12-fold branching pathway. Chem. Sci. 2, 2232-2235 (2011
    • (2011) Chem. Sci. , vol.2 , pp. 2232-2235
    • Robbins, D.1
  • 29
    • 84900412775 scopus 로고    scopus 로고
    • Diversity-oriented synthesis as a tool for identifying new modulators of mitosis
    • Ibbeson, B. M. et al. Diversity-oriented synthesis as a tool for identifying new modulators of mitosis. Nat. Commun. 5, 3155 (2014
    • (2014) Nat. Commun. , vol.5 , pp. 3155
    • Ibbeson, B.M.1
  • 30
    • 79955688676 scopus 로고    scopus 로고
    • Generation of anti-trypanosomal agents through concise synthesis and structural diversification of sesquiterpene analogues
    • Oguri, H. et al. Generation of anti-trypanosomal agents through concise synthesis and structural diversification of sesquiterpene analogues. J. Am. Chem. Soc. 133, 7096-7105 (2011
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 7096-7105
    • Oguri, H.1
  • 31
    • 84884837727 scopus 로고    scopus 로고
    • A strategy for the diversity-oriented synthesis of macrocyclic scaffolds using multidimensional coupling
    • Beckmann, H. S. G. et al. A strategy for the diversity-oriented synthesis of macrocyclic scaffolds using multidimensional coupling. Nat. Chem. 5, 861-867 (2013
    • (2013) Nat. Chem. , vol.5 , pp. 861-867
    • Beckmann, H.S.G.1
  • 32
    • 84893020694 scopus 로고    scopus 로고
    • Probing chemical space with alkaloid-inspired libraries
    • McLeod, M. C. et al. Probing chemical space with alkaloid-inspired libraries. Nat. Chem. 6, 133-140 (2014
    • (2014) Nat. Chem. , vol.6 , pp. 133-140
    • McLeod, M.C.1
  • 33
    • 34250213240 scopus 로고    scopus 로고
    • Pattern recognition in retrosynthetic analysis: Snapshots in total synthesis
    • DOI 10.1021/jo070871s
    • Wilson, R. M. & Danishefsky, S. J. Pattern recognition in retrosynthetic analysis: Snapshots in total synthesis. J. Org. Chem. 72, 4293-4305 (2007 (Pubitemid 46903297)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.12 , pp. 4293-4305
    • Wilson, R.M.1    Danishefsky, S.J.2
  • 34
    • 84869412367 scopus 로고    scopus 로고
    • Total synthesis of (±)-maoecrystal v
    • Peng, F. & Danishefsky, S. J. Total synthesis of (±)- maoecrystal V. J. Am. Chem. Soc. 134, 18860-18867 (2012
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 18860-18867
    • Peng, F.1    Danishefsky, S.J.2
  • 35
    • 11144328091 scopus 로고    scopus 로고
    • The Lycopodium alkaloids
    • DOI 10.1039/b409720n
    • Ma, X. & Gang, D. R. The Lycopodium alkaloids. Nat. Prod. Rep. 21, 752-772 (2004 (Pubitemid 40033085)
    • (2004) Natural Product Reports , vol.21 , Issue.6 , pp. 752-772
    • Ma, X.1    Gang, D.R.2
  • 37
    • 62949139899 scopus 로고    scopus 로고
    • Role of huperzine A in the treatment of Alzheimer's disease
    • Desilets, A. R., Gickas, J. J. & Dunican, K. C. Role of huperzine A in the treatment of Alzheimer's disease. Ann. Pharmacother. 43, 514-518 (2009
    • (2009) Ann. Pharmacother. , vol.43 , pp. 514-518
    • Desilets, A.R.1    Gickas, J.J.2    Dunican, K.C.3
  • 38
    • 0034703296 scopus 로고    scopus 로고
    • Serratezomines A-C new alkaloids from Lycopodium serratum var. Serratum
    • Morita, H., Arisaka, M., Yoshida, N. & Kobayashi, J. Serratezomines A-C, new alkaloids from Lycopodium serratum var. serratum. J. Org. Chem 65, 6241-6245 (2000
    • (2000) J. Org. Chem , vol.65 , pp. 6241-6245
    • Morita, H.1    Arisaka, M.2    Yoshida, N.3    Kobayashi, J.4
  • 39
    • 84875915721 scopus 로고    scopus 로고
    • Challenges and strategies to the total syntheses of fawcettimine-type and serratinine-type Lycopodium alkaloids
    • Wang, X., Li, H. & Lei, X. Challenges and strategies to the total syntheses of fawcettimine-type and serratinine-type Lycopodium alkaloids. Synlett 24, 1032-1043 (2013
    • (2013) Synlett , vol.24 , pp. 1032-1043
    • Wang, X.1    Li, H.2    Lei, X.3
  • 40
    • 84891485623 scopus 로고    scopus 로고
    • Heathcock-inspired strategies for the synthesis of fawcettimine-type Lycopodium alkaloids
    • Murphy, R. A. & Sarpong, R. Heathcock-inspired strategies for the synthesis of fawcettimine-type Lycopodium alkaloids. Chem. Eur. J. 20, 42-56 (2014
    • (2014) Chem. Eur. J. , vol.20 , pp. 42-56
    • Murphy, R.A.1    Sarpong, R.2
  • 42
    • 64049105024 scopus 로고    scopus 로고
    • Lycojapodine A, a novel alkaloid from Lycopodium japonicum
    • He, J. et al. Lycojapodine A, a novel alkaloid from Lycopodium japonicum. Org. Lett. 11, 1397-1400 (2009
    • (2009) Org. Lett. , vol.11 , pp. 1397-1400
    • He, J.1
  • 44
    • 0242628368 scopus 로고    scopus 로고
    • Sieboldine A, a Novel Tetracyclic Alkaloid from Lycopodium sieboldii, Inhibiting Acetylcholinesterase
    • DOI 10.1021/ol035560s
    • Hirasawa, Y., Morita, H., Shiro, M. & Kobayashi, J. Sieboldine A, a novel tetracyclic alkaloid from Lycopodium sieboldii, inhibiting acetylcholinesterase. Org. Lett. 5, 3991-3993 (2003 (Pubitemid 37412184)
    • (2003) Organic Letters , vol.5 , Issue.21 , pp. 3991-3993
    • Hirasawa, Y.1    Morita, H.2    Shiro, M.3    Kobayashi, J.4
  • 46
    • 79960959375 scopus 로고    scopus 로고
    • Ten new fawcettimine-related alkaloids from three species of Lycopodium
    • Katakawa, K. et al. Ten new fawcettimine-related alkaloids from three species of Lycopodium. Tetrahedron 67, 6561-6567 (2011
    • (2011) Tetrahedron , vol.67 , pp. 6561-6567
    • Katakawa, K.1
  • 47
    • 0037064495 scopus 로고    scopus 로고
    • Seven new Lycopodium alkaloids, lycoposerramines-C, -D, -E, -P, -Q, -S, and -U, from Lycopodium serratum Thunb
    • DOI 10.1016/S0040-4039(02)02026-9, PII S0040403902020269
    • Takayama, H., Katakawa, K., Kitajima, M., Yamaguchi, K. & Aimi, N. Seven new Lycopodium alkaloids, lycoposerramines-C,-D,-E,-P,-Q,-S, and-U, from Lycopodium serratum Thunb. Tetrahedron Lett. 43, 8307-8311 (2002 (Pubitemid 35223361)
    • (2002) Tetrahedron Letters , vol.43 , Issue.46 , pp. 8307-8311
    • Takayama, H.1    Katakawa, K.2    Kitajima, M.3    Yamaguchi, K.4    Aimi, N.5
  • 48
    • 84866260989 scopus 로고    scopus 로고
    • Synthesis of 4-hydroxy-5-methyl-and 4-hydroxy-6-methylcyclohexenones by PdII-catalyzed oxidation and lipasecatalyzed hydrolysis
    • Meister, A. C., Nieger, M. & Bräse, S. Synthesis of 4-hydroxy-5-methyl-and 4-hydroxy-6-methylcyclohexenones by PdII-catalyzed oxidation and lipasecatalyzed hydrolysis. Eur. J. Org. Chem. 5373-5380 (2012
    • (2012) Eur. J. Org. Chem. , pp. 5373-5380
    • Meister, A.C.1    Nieger, M.2    Bräse, S.3
  • 49
    • 0037035006 scopus 로고    scopus 로고
    • Studies toward the total synthesis of garsubellin A: A concise synthesis of the 18-epi-tricyclic core
    • Usuda, H., Kanai, M. & Shibasaki, M. Studies toward the total synthesis of garsubellin A: A concise synthesis of the 18-epi-tricyclic core. Org. Lett. 4, 859-862 (2002
    • (2002) Org. Lett. , vol.4 , pp. 859-862
    • Usuda, H.1    Kanai, M.2    Shibasaki, M.3
  • 50
    • 84855445467 scopus 로고    scopus 로고
    • Total syntheses of lycopodium alkaloids (+)-fawcettimine, (+)-fawcettidine, and (-)-8-deoxyserratinine
    • Li, H., Wang, X. & Lei, X. Total syntheses of Lycopodium alkaloids (+)-fawcettimine, (+)-fawcettidine, and (-)-8-deoxyserratinine. Angew. Chem. Int. Ed. 51, 491-495 (2012
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 491-495
    • Li, H.1    Wang, X.2    Lei, X.3
  • 51
    • 4644228335 scopus 로고    scopus 로고
    • 4
    • DOI 10.1021/ol0400342
    • Yu, W., Mei, Y., Kang, Y., Hua, Z. & Jin, Z. Improved procedure for the oxidative cleavage of olefins by OsO4-NaIO4. Org. Lett. 6, 3217-3219 (2004 (Pubitemid 39297303)
    • (2004) Organic Letters , vol.6 , Issue.19 , pp. 3217-3219
    • Yu, W.1    Mei, Y.2    Kang, Y.3    Hua, Z.4    Jin, Z.5
  • 52
    • 0037178353 scopus 로고    scopus 로고
    • A biomimetic transformation of serratinine into serratezomine A through a modified Polonovski reaction
    • DOI 10.1021/jo025821w
    • Morita, H. & Kobayashi, J. A biomimetic transformation of serratinine into serratezomine A through a modified Polonovski reaction. J. Org. Chem. 67, 5378-5381 (2002 (Pubitemid 34793213)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.15 , pp. 5378-5381
    • Morita, H.1    Kobayashi, J.2
  • 53
    • 22144480983 scopus 로고    scopus 로고
    • An efficient synthesis of achiral and chiral 1,2,4-triazolium salts: Bench stable precursors for N-heterocyclic carbenes
    • DOI 10.1021/jo050645n
    • Kerr, M. S., De Alaniz, J. R. & Rovis, T. An efficient synthesis of achiral and chiral 1,2,4-triazolium salts: Bench stable precursors for N-heterocyclic carbenes. J. Org. Chem. 70, 5725-5728 (2005 (Pubitemid 40980786)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.14 , pp. 5725-5728
    • Kerr, M.S.1    Read De Alaniz, J.2    Rovis, T.3
  • 54
    • 0033786545 scopus 로고    scopus 로고
    • Synthesis of bicyclic azacompounds (3-dimethylcarbamoyloxyphenyl) substituted as acetylcholinesterase inhibitors
    • Borioni, A., Del Guidice, M. R., Mustazza, C. & Gatta, F. Synthesis of bicyclic azacompounds (3-dimethylcarbamoyloxyphenyl) substituted as acetylcholinesterase inhibitors. J. Heterocycl. Chem. 37, 799-810 (2000
    • (2000) J. Heterocycl. Chem. , vol.37 , pp. 799-810
    • Borioni, A.1    Del Guidice, M.R.2    Mustazza, C.3    Gatta, F.4
  • 55
    • 79956071522 scopus 로고    scopus 로고
    • Application of the Helquist annulation in Lycopodium alkaloid synthesis: Unified total syntheses of (-)-8-deoxyserratinine, (+)-fawcettimine, and (+)-lycoflexine
    • Yang, Y.-R., Shen, L., Huang, J.-Z., Xu, T. & Wei, K. Application of the Helquist annulation in Lycopodium alkaloid synthesis: Unified total syntheses of (-)-8-deoxyserratinine, (+)-fawcettimine, and (+)-lycoflexine. J. Org. Chem. 76, 3684-3690 (2011
    • (2011) J. Org. Chem. , vol.76 , pp. 3684-3690
    • Yang, Y.-R.1    Shen, L.2    Huang, J.-Z.3    Xu, T.4    Wei, K.5
  • 56
    • 77958035710 scopus 로고    scopus 로고
    • Synthesis of the lycopodium alkaloid (+)-lycoflexine
    • Ramharter, J., Weinstabl, H. & Mulzer, J. Synthesis of the Lycopodium alkaloid (+)-lycoflexine. J. Am. Chem. Soc. 132, 14338-14339 (2010
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 14338-14339
    • Ramharter, J.1    Weinstabl, H.2    Mulzer, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.