메뉴 건너뛰기




Volumn 41, Issue 1, 2008, Pages 3-11

Practical organocatalysis with (S)- and (r)-5-pyrrolidin-2-yl-1H-tetrazoles

Author keywords

[No Author keywords available]

Indexed keywords


EID: 45349090522     PISSN: 00025100     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (56)

References (177)
  • 8
  • 19
    • 4143094833 scopus 로고    scopus 로고
    • See also the following special issues on organocatalysis: (s) Asymmetric Organocatalysis. Houk, K. N., List, B., Eds.; Acc. Chem. Res. 2004, 37, Issue 8 (August 2004); pp 487-631.
    • See also the following special issues on organocatalysis: (s) Asymmetric Organocatalysis. Houk, K. N., List, B., Eds.; Acc. Chem. Res. 2004, 37, Issue 8 (August 2004); pp 487-631.
  • 20
    • 45349103017 scopus 로고    scopus 로고
    • Organic Catalysis. Adv. Synth. Catal. 2004, 346, Issues 9-10 (August 2004); pp 1007-1249.
    • (t) Organic Catalysis. Adv. Synth. Catal. 2004, 346, Issues 9-10 (August 2004); pp 1007-1249.
  • 34
    • 45349099597 scopus 로고    scopus 로고
    • For an alternative method to form the tetrazole ring system, see: h, Intl. Patent WO /014602 A1, February 17, 2005
    • For an alternative method to form the tetrazole ring system, see: (h) Sedelmeier, G. Intl. Patent WO 2005/014602 A1, February 17, 2005.
    • (2005)
    • Sedelmeier, G.1
  • 35
    • 45349097606 scopus 로고    scopus 로고
    • Intl. Patent WO 2007/009716, January 25
    • (i) Sedelmeier, G.; Aurreggi, V. Intl. Patent WO 2007/009716, January 25, 2007.
    • (2007)
    • Sedelmeier, G.1    Aurreggi, V.2
  • 40
    • 45349104513 scopus 로고    scopus 로고
    • German Patent DE 2014757.3, October 7, 1971
    • (a) Eder, U.; Wiechert, R.; Sauer, G. German Patent DE 2014757.3, October 7, 1971.
    • Eder, U.1    Wiechert, R.2    Sauer, G.3
  • 41
    • 45349101110 scopus 로고
    • German Patent DE 2102623 C2, July 29
    • (b) Hajos, Z. G.; Parrish, D. R. German Patent DE 2102623 C2, July 29, 1971.
    • (1971)
    • Hajos, Z.G.1    Parrish, D.R.2
  • 51
    • 33646056099 scopus 로고    scopus 로고
    • For the reaction of 1,2-diketones and ketones, see
    • (h) For the reaction of 1,2-diketones and ketones, see Samanta, S.; Zhao, C.-G. Tetrahedron Lett. 2006, 47, 3383.
    • (2006) Tetrahedron Lett , vol.47 , pp. 3383
    • Samanta, S.1    Zhao, C.-G.2
  • 52
    • 33745893522 scopus 로고    scopus 로고
    • Other amino acid tetrazole derivatives have also been examined and found to compare favourably with their unmodified amino acid counterparts in the intermolecular aldol reaction process: Córdova, A, Zou, W, Dziedzic, P, Ibrahem, I, Reyes, E, Xu, Y. Chem, Eur. J. 2006, 12, 5383
    • (i) Other amino acid tetrazole derivatives have also been examined and found to compare favourably with their unmodified amino acid counterparts in the intermolecular aldol reaction process: Córdova, A.; Zou, W.; Dziedzic, P.; Ibrahem, I.; Reyes, E.; Xu, Y. Chem. - Eur. J. 2006, 12, 5383.
  • 59
    • 24044462953 scopus 로고    scopus 로고
    • A Density Functional Theory (DFT) study has since supported these findings
    • A Density Functional Theory (DFT) study has since supported these findings: Arnó, M.; Zaragozá, R. J.; Domingo, L. R. Tetrahedron: Asymmetry 2005, 16, 2764.
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 2764
    • Arnó, M.1    Zaragozá, R.J.2    Domingo, L.R.3
  • 91
    • 45349109238 scopus 로고    scopus 로고
    • Loadings of 5% were generally used for operational simplicity
    • Loadings of 5% were generally used for operational simplicity.
  • 102
    • 5144224358 scopus 로고    scopus 로고
    • For recent related publications demonstrating the utility of alternative catalytic species, see: a
    • For recent related publications demonstrating the utility of alternative catalytic species, see: (a) Andrey, O.; Alexakis, A.; Tomassini, A.; Bernardinelli, G. Adv. Synth. Catal. 2004, 346, 1147.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 1147
    • Andrey, O.1    Alexakis, A.2    Tomassini, A.3    Bernardinelli, G.4
  • 116
    • 24944514433 scopus 로고    scopus 로고
    • For the latest improvements to this organocatalytic process, see: e
    • For the latest improvements to this organocatalytic process, see: (e) Prieto, A.; Halland, N.; Jørgensen, K. A. Org. Lett. 2005, 7, 3897.
    • (2005) Org. Lett , vol.7 , pp. 3897
    • Prieto, A.1    Halland, N.2    Jørgensen, K.A.3
  • 118
    • 0027943133 scopus 로고
    • For use of other catalytic systems in this reaction, see: a
    • For use of other catalytic systems in this reaction, see: (a) Kawara, A.; Taguchi, T. Tetrahedron Lett. 1994, 35, 8805.
    • (1994) Tetrahedron Lett , vol.35 , pp. 8805
    • Kawara, A.1    Taguchi, T.2
  • 125
    • 45349104254 scopus 로고    scopus 로고
    • Wascholowski, V.; Rahbek Knudsen, K.; Mitchell, C. E. T.; Ley, S. V. University of Cambridge, Cambridge, U.K. Unpublished work, 2007.
    • Wascholowski, V.; Rahbek Knudsen, K.; Mitchell, C. E. T.; Ley, S. V. University of Cambridge, Cambridge, U.K. Unpublished work, 2007.
  • 145
    • 84980161144 scopus 로고
    • For a selection of publications in this area, see: a
    • For a selection of publications in this area, see: (a) Kocór, M.; Kroszczyński, W. Synthesis 1976, 813.
    • (1976) Synthesis , pp. 813
    • Kocór, M.1    Kroszczyński, W.2
  • 159
    • 0041733541 scopus 로고    scopus 로고
    • For prior work in this area using L-proline (1) as catalyst, see: (a) Brown, S. P.; Brochu, M. P.; Sinz, C. J.; MacMillan, D. W. C. J. Am. Chem. Soc. 2003, 125, 10808.
    • For prior work in this area using L-proline (1) as catalyst, see: (a) Brown, S. P.; Brochu, M. P.; Sinz, C. J.; MacMillan, D. W. C. J. Am. Chem. Soc. 2003, 125, 10808.
  • 166
    • 33947198541 scopus 로고    scopus 로고
    • For a recent minireview on asymmetric organocatalytic domino reactions, see
    • For a recent minireview on asymmetric organocatalytic domino reactions, see Enders, D.; Grondal, C.; Hüttl, M. R. M. Angew. Chem., Int. Ed. 2007, 46, 1570.
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 1570
    • Enders, D.1    Grondal, C.2    Hüttl, M.R.M.3
  • 167
  • 169
    • 0001436716 scopus 로고    scopus 로고
    • (c) Katz, L. Chem. Rev. 1997, 97, 2557.
    • (1997) Chem. Rev , vol.97 , pp. 2557
    • Katz, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.