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Volumn , Issue 6, 2008, Pages 971-974

Synthesis and characterization of cyclopropylpolyketides: A combined experimental and theoretical study

Author keywords

Conformations; Cyclopropanes; Density functional theory; Ketones

Indexed keywords


EID: 53649088617     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200701140     Document Type: Article
Times cited : (3)

References (26)
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    • Peralkylpolyketides were previously prepared in very low yields based on the base-mediated ring cleavage of 2,2,4-trimethyl-3-hydroxypentenoic acid β-lactone: K. D. Berlin, R. B. Hanson, J. Org. Chem. 1967, 32, 1763
    • Peralkylpolyketides were previously prepared in very low yields based on the base-mediated ring cleavage of 2,2,4-trimethyl-3-hydroxypentenoic acid β-lactone: K. D. Berlin, R. B. Hanson, J. Org. Chem. 1967, 32, 1763.
  • 9
    • 0013536543 scopus 로고    scopus 로고
    • The formation of a triketide as a side-product was previously claimed, but the product has not been unambiguously identified: J. M. Stewart, G. K. Pagenkopf, J. Org. Chem. 1969, 34, 7.
    • The formation of a triketide as a side-product was previously claimed, but the product has not been unambiguously identified: J. M. Stewart, G. K. Pagenkopf, J. Org. Chem. 1969, 34, 7.
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    • Zh. Org. Khim. 1983, 19, 541.
    • (1983) Zh. Org. Khim , vol.19 , pp. 541
  • 20
    • 9644310079 scopus 로고    scopus 로고
    • The synthesis of 2a and 2b is known; however, compound 2a was not completely characterized.N. S. Zefirov, S. I. Kozhushkov, T. S. Kuznetsova, Chem. Heterocycl. Compd. (Engl. Transl.) 1983, 19, 644;
    • The synthesis of 2a and 2b is known; however, compound 2a was not completely characterized.N. S. Zefirov, S. I. Kozhushkov, T. S. Kuznetsova, Chem. Heterocycl. Compd. (Engl. Transl.) 1983, 19, 644;
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    • M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery, Jr, T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain, O. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. Ortiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M
    • M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery, Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain, O. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. Ortiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, C. Gonzalez, J. A. Pople, Gaussian 03, Revision C.02, Gaussian, Inc., Wallingford CT, 2004.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.