메뉴 건너뛰기




Volumn 9, Issue , 2013, Pages 1111-1118

C-C bond formation catalyzed by natural gelatin and collagen proteins

Author keywords

Biocatalysis; Carbon carbon bond formation; Gelatin; Henry reaction; Protein

Indexed keywords


EID: 84878898895     PISSN: None     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.9.123     Document Type: Article
Times cited : (27)

References (32)
  • 2
    • 77956884943 scopus 로고    scopus 로고
    • doi:10.1016/j.colsurfa.2010.08.029
    • Kang, S.-Z.; Wu, T.; Li, X.; Mu, J. Colloids Surf., A 2010, 369, 268-271. doi:10.1016/j.colsurfa.2010.08.029
    • (2010) Colloids Surf., A , vol.369 , pp. 268-271
    • Kang, S.-Z.1    Wu, T.2    Li, X.3    Mu, J.4
  • 5
    • 0035804426 scopus 로고    scopus 로고
    • The Henry reaction: Recent examples
    • DOI 10.1016/S0040-4020(00)00965-0, PII S0040402000009650
    • Luzzio, F. A. Tetrahedron 2001, 57, 915-945. doi:10.1016/S0040-4020(00) 00965-0 (Pubitemid 32121979)
    • (2001) Tetrahedron , vol.57 , Issue.6 , pp. 915-945
    • Luzzio, F.A.1
  • 7
    • 33846593979 scopus 로고    scopus 로고
    • Catalytic asymmetric Henry reaction
    • DOI 10.1016/j.tetasy.2006.12.005, PII S0957416606009074
    • Boruwa, J.; Gogoi, N.; Saikia, P. P.; Barua, N. C. Tetrahedron: Asymmetry 2006, 17, 3315-3326. doi:10.1016/j.tetasy.2006.12.005 (Pubitemid 46185987)
    • (2006) Tetrahedron Asymmetry , vol.17 , Issue.24 , pp. 3315-3326
    • Boruwa, J.1    Gogoi, N.2    Saikia, P.P.3    Barua, N.C.4
  • 14
    • 77958009739 scopus 로고    scopus 로고
    • doi:10.2174/138527210792927591
    • Wu, Q.; Liu, B.-K.; Lin, X.-F. Curr. Org. Chem. 2010, 14, 1966-1988. doi:10.2174/138527210792927591
    • (2010) Curr. Org. Chem. , vol.14 , pp. 1966-1988
    • Wu, Q.1    Liu, B.-K.2    Lin, X.-F.3
  • 17
    • 33749474246 scopus 로고
    • See for gelatin-catalyzed hydrolysis of 4-nitrophenyl acetate and references therein
    • Sergeev, B. M.; Konstantinova, N. R.; Sergeev, G. B. Kinet. Catal. 1991, 32, 1060-1066. See for gelatin-catalyzed hydrolysis of 4-nitrophenyl acetate and references therein.
    • (1991) Kinet. Catal. , vol.32 , pp. 1060-1066
    • Sergeev, B.M.1    Konstantinova, N.R.2    Sergeev, G.B.3
  • 19
    • 23544432250 scopus 로고
    • doi:10.1016/0006-3002(56)90325-0
    • Bello, L. J. Biochim. Biophys. Acta 1956, 20, 426-427. doi:10.1016/0006-3002(56)90325-0
    • (1956) Biochim. Biophys. Acta , vol.20 , pp. 426-427
    • Bello, L.J.1
  • 22
    • 33847638971 scopus 로고    scopus 로고
    • Aqua-organocatalyzed direct asymmetric aldol reaction with acyclic amino acids and organic bases with control of diastereo- and enantioselectivity
    • DOI 10.1016/j.tetasy.2007.01.025, PII S0957416607000833
    • Amedjkouh, M. Tetrahedron: Asymmetry 2007, 18, 390-395. doi:10.1016/j.tetasy.2007.01.025 (Pubitemid 46367639)
    • (2007) Tetrahedron Asymmetry , vol.18 , Issue.3 , pp. 390-395
    • Amedjkouh, M.1
  • 23
    • 33846567129 scopus 로고    scopus 로고
    • Stereoselective aldol reactions catalyzed by acyclic amino acids in aqueous micelles
    • DOI 10.1002/hlca.200790003
    • Deng, D.-S.; Cai,J. Helv. Chim. Acta 2007, 90, 114-120. doi:10.1002/hlca.200790003 (Pubitemid 46184121)
    • (2007) Helvetica Chimica Acta , vol.90 , Issue.1 , pp. 114-120
    • Deng, D.-S.1    Cai, J.2
  • 24
    • 33846039446 scopus 로고    scopus 로고
    • Amino acid mediated intramolecular asymmetric aldol reaction to construct a new chiral bicyclic enedione containing a seven-membered ring: Remarkable inversion of enantioselectivity compared to the six-membered ring example
    • DOI 10.1021/jo061824n
    • Nagamine, T.; Inomata, K.; Endo, Y.; Paquette, L. A. J. Org. Chem. 2007, 72, 123-131. doi:10.1021/jo061824n (Pubitemid 46068211)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.1 , pp. 123-131
    • Nagamine, T.1    Inomata, K.2    Endo, Y.3    Paquette, L.A.4
  • 25
    • 77956394854 scopus 로고    scopus 로고
    • doi:10.1007/s10562-010-0351-y
    • Deng, D.; Liu, P.; Ji, B.; Fu, W.; Li, L. Catal. Lett. 2010, 137, 163-170. doi:10.1007/s10562-010-0351-y
    • (2010) Catal. Lett. , vol.137 , pp. 163-170
    • Deng, D.1    Liu, P.2    Ji, B.3    Fu, W.4    Li, L.5
  • 27
    • 84860195253 scopus 로고    scopus 로고
    • doi:10.1021/ol300754n
    • Rohr, K.; Mahrwald, R. Org. Lett. 2012, 14, 2180-2183. doi:10.1021/ol300754n
    • (2012) Org. Lett. , vol.14 , pp. 2180-2183
    • Rohr, K.1    Mahrwald, R.2
  • 32
    • 0031380647 scopus 로고    scopus 로고
    • doi:10.1088/0957-4484/8/4/004
    • Jeong, S. W.; Shinkai, S. Nanotechnology 1997, 8, 179-183. doi:10.1088/0957-4484/8/4/004
    • (1997) Nanotechnology , vol.8 , pp. 179-183
    • Jeong, S.W.1    Shinkai, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.