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Volumn 9, Issue , 2013, Pages 2233-2241

Elucidation of the regio- and chemoselectivity of enzymatic allylic oxidations with Pleurotus sapidus - Conversion of selected spirocyclic terpenoids and computational analysis

Author keywords

Allylic oxidation; CH activation; Chiral separation; Enones; Flavors; Natural products; Terpenes

Indexed keywords


EID: 84888604215     PISSN: None     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.9.262     Document Type: Article
Times cited : (15)

References (49)
  • 3
    • 0002812520 scopus 로고
    • 2.1 - Oxidation Adjacent to C=C Bonds. in
    • Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford doi:10.1016/B978-0-08- 052349-1.00184-0
    • Page, P. C. B.; McCarthy, T. J. 2.1 - Oxidation Adjacent to C=C Bonds. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 7, pp 83-117. doi:10.1016/B978-0-08-052349-1.00184-0
    • (1991) Comprehensive Organic Synthesis , vol.7 , pp. 83-117
    • Page, P.C.B.1    McCarthy, T.J.2
  • 4
    • 84878131497 scopus 로고    scopus 로고
    • doi:10.1055/s-0033-1338426
    • Nakamura, A.; Nakada, M. Synthesis 2013, 45, 1421-1451. doi:10.1055/s-0033-1338426
    • (2013) Synthesis , vol.45 , pp. 1421-1451
    • Nakamura, A.1    Nakada, M.2
  • 5
    • 84881480588 scopus 로고    scopus 로고
    • doi:10.1055/s-0033-1338491
    • Weidmann, V.; Maison, W. Synthesis 2013, 45, 2201-2221. doi:10.1055/s-0033-1338491
    • (2013) Synthesis , vol.45 , pp. 2201-2221
    • Weidmann, V.1    Maison, W.2
  • 7
    • 0037185537 scopus 로고    scopus 로고
    • Copper catalyzed allylic oxidation with peresters
    • DOI 10.1016/S0040-4020(01)01172-3, PII S0040402001011723
    • Andrus, M. B.; Lashley, J. C. Tetrahedron 2002, 58, 845-866. doi:10.1016/S0040-4020(01)01172-3 (Pubitemid 34093831)
    • (2002) Tetrahedron , vol.58 , Issue.5 , pp. 845-866
    • Andrus, M.B.1    Lashley, J.C.2
  • 10
    • 44049105915 scopus 로고    scopus 로고
    • Osmium and palladium: Complementary metals in alkene activation and oxidation
    • DOI 10.1055/s-2008-1067031, E20307SS
    • Christie, S. D. R.; Warrington, A. D. Synthesis 2008, 1325-1341. doi:10.1055/s-2008-1067031 (Pubitemid 351709847)
    • (2008) Synthesis , Issue.9 , pp. 1325-1341
    • Christie, S.D.R.1    Warrington, A.D.2
  • 11
    • 0037124966 scopus 로고    scopus 로고
    • Zeolite encapsulated ruthenium and cobalt schiff base complexes catalyzed allylic oxidation of α-pinene
    • DOI 10.1016/S1381-1169(02)00010-9, PII S1381116902000109
    • Joseph, T.; Sawant, D. P.; Gopinath, C. S.; Halligudi, S. B. J. Mol. Catal. A: Chem. 2002, 184, 289-299. doi:10.1016/S1381-1169(02)00010-9 (Pubitemid 34760358)
    • (2002) Journal of Molecular Catalysis A: Chemical , vol.184 , Issue.1-2 , pp. 289-299
    • Joseph, T.1    Sawant, D.P.2    Gopinath, C.S.3    Halligudi, S.B.4
  • 13
    • 70350289386 scopus 로고    scopus 로고
    • doi:10.1007/s10529-009-0083-5
    • Berger, R. G. Biotechnol. Lett. 2009, 31, 1651-1659. doi:10.1007/s10529- 009-0083-5
    • (2009) Biotechnol. Lett. , vol.31 , pp. 1651-1659
    • Berger R., .G.1
  • 14
    • 36349031083 scopus 로고    scopus 로고
    • Steroids: Partial synthesis in medicinal chemistry
    • DOI 10.1039/b705948p
    • Hanson, J. R. Nat. Prod. Rep. 2007, 24, 1342-1349. doi:10.1039/b705948p (Pubitemid 350151356)
    • (2007) Natural Product Reports , vol.24 , Issue.6 , pp. 1342-1349
    • Hanson, J.R.1
  • 17
    • 33750593724 scopus 로고    scopus 로고
    • Catalytic oxidative processes in steroid chemistry: Allylic oxidation, β-Selective expoxidation, alcohol oxidation and remote functionalization reactions
    • DOI 10.2174/138527206778742641
    • Salvador, J. A. R.; Silvestre, S. M.; Moreira, V. M. Curr. Org. Chem. 2006, 10, 2227-2257. doi:10.2174/138527206778742641 (Pubitemid 44679300)
    • (2006) Current Organic Chemistry , vol.10 , Issue.17 , pp. 2227-2257
    • Salvador, J.A.R.1    Silvestre, S.M.2    Moreira, V.M.3
  • 18
    • 1542642335 scopus 로고
    • doi:10.1021/cr00009a005
    • Muzart, J. Chem. Rev. 1992, 92, 113-140. doi:10.1021/cr00009a005
    • (1992) Chem. Rev. , vol.92 , pp. 113-140
    • Muzart, J.1
  • 19
    • 70049096071 scopus 로고    scopus 로고
    • doi:10.2174/157019309787316120
    • Muzart, J. Mini-Rev. Org. Chem. 2009, 6, 9-20. doi:10.2174/ 157019309787316120
    • (2009) Mini-Rev. Org. Chem. , vol.6 , pp. 9-20
    • Muzart, J.1
  • 20
    • 24144496039 scopus 로고    scopus 로고
    • Efficient terpene hydroxylation catalysts based upon P450 enzymes derived from actinomycetes
    • DOI 10.1039/b506159h
    • Çelik, A.; Flitsch, S. L.; Turner, N. J. Org. Biomol. Chem. 2005, 3, 2930-2934. doi:10.1039/b506159h (Pubitemid 41239069)
    • (2005) Organic and Biomolecular Chemistry , vol.3 , Issue.16 , pp. 2930-2934
    • Celik, A.1    Flitsch, S.L.2    Turner, N.J.3
  • 21
  • 22
    • 0036900263 scopus 로고    scopus 로고
    • The production of fine chemicals by biotransformations
    • DOI 10.1016/S0958-1669(02)00360-9
    • Straathof, A. J. J.; Panke, S.; Schmid, A. Curr. Opin. Biotechnol. 2002, 13, 548-556. doi:10.1016/S0958-1669(02)00360-9 (Pubitemid 35448055)
    • (2002) Current Opinion in Biotechnology , vol.13 , Issue.6 , pp. 548-556
    • Straathof, A.J.J.1    Panke, S.2    Schmid, A.3
  • 23
    • 65249128025 scopus 로고    scopus 로고
    • doi:10.1016/j.cbpa.2009.01.018
    • Tao, J.; Xu, J.-H. Curr. Opin. Chem. Biol. 2009, 13, 43-50. doi:10.1016/j.cbpa.2009.01.018
    • (2009) Curr. Opin. Chem. Biol. , vol.13 , pp. 43-50
    • Tao, J.1    Xu, J.-H.2
  • 27
    • 0032965706 scopus 로고    scopus 로고
    • Effects of R-(+)-limonene on submerged cultures of the terpene transforming basidiomycete Pleurotus sapidus
    • DOI 10.1016/S0168-1656(99)00040-1, PII S0168165699000401
    • Onken, J.; Berger, R. G. J. Biotechnol. 1999, 69, 163-168. doi:10.1016/S0168-1656(99)00040-1 (Pubitemid 29206497)
    • (1999) Journal of Biotechnology , vol.69 , Issue.2-3 , pp. 163-168
    • Onken, J.1    Berger, R.G.2
  • 33
    • 0000696372 scopus 로고
    • doi:10.1021/jo01034a055
    • Wiberg, K. B.; Nielsen, S. D. J. Org. Chem. 1964, 29, 3353-3361. doi:10.1021/jo01034a055
    • (1964) J. Org. Chem. , vol.29 , pp. 3353-3361
    • Wiberg, K.B.1    Nielsen, S.D.2
  • 35
    • 0032516292 scopus 로고    scopus 로고
    • Cyclic vs. Acyclic allylic hydrogen abstraction: An entropy motivated process?
    • DOI 10.1016/S0040-4020(98)00215-4, PII S0040402098002154
    • Rothenberg, G.; Sasson, Y. Tetrahedron 1998, 54, 5417-5422. doi:10.1016/S0040-4020(98)00215-4 (Pubitemid 28204499)
    • (1998) Tetrahedron , vol.54 , Issue.20 , pp. 5417-5422
    • Rothenberg, G.1    Sasson, Y.2
  • 39
    • 77954697532 scopus 로고    scopus 로고
    • doi:10.1039/c0cc00481b
    • Huang, C.; Liu, B. Chem. Commun. 2010, 46, 5280-5282. doi:10.1039/c0cc00481b
    • (2010) Chem. Commun. , vol.46 , pp. 5280-5282
    • Huang, C.1    Liu, B.2
  • 42
    • 13344284853 scopus 로고
    • doi:10.1246/bcsj.54.1573
    • Kato, T.; Kondo, H. Bull. Chem. Soc. Jpn. 1981, 54, 1573-1574. doi:10.1246/bcsj.54.1573
    • (1981) Bull. Chem. Soc. Jpn. , vol.54 , pp. 1573-1574
    • Kato, T.1    Kondo, H.2
  • 46
    • 0017876331 scopus 로고
    • Vitispiranes, important constituents of vanilla aroma
    • DOI 10.1002/hlca.19780610326
    • Schulte-Elte, K. H.; Gautschi, F.; Renold, W.; Hauser, A.; Frankhauser, P.; Limacher, J.; Ohloff, G. Helv. Chim. Acta 1978, 61, 1125-1133. doi:10.1002/hlca.19780610326 (Pubitemid 8319889)
    • (1978) Helvetica Chimica Acta , vol.61 , Issue.3 , pp. 1125-1133
    • Schulte Elte, K.H.1    Gautschi, F.2    Renold, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.