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Volumn , Issue 4, 2003, Pages 505-508

A facile asymmetric synthesis of tetrahydroisoquinoline and tryptoline derivatives with a quaternary carbon center at C(3)

Author keywords

Amino acids; Asymmetric synthesis; Axial chirality; Heterocycles; Pictet Spengler reaction

Indexed keywords

CARBON; DERIVATIVES; SYNTHESIS (CHEMICAL);

EID: 0037243455     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-37648     Document Type: Article
Times cited : (20)

References (21)
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    • 0034927038 scopus 로고    scopus 로고
    • For recent examples see: (a) Spengler, J.; Schedel, H.; Sieler, J.; Quaedflieg, P. J. L. M.; Broxterman, Q. B.; Duchateau, A. L. L.; Barger, K. Synthesis 2001, 1513. (b) Meziane, M. A. A.; Royer, S.; Bazureau, J. P. Tetrahedron Lett. 2001, 42, 1017. (c) Davis, F. A.; Mohanty, P. K.; Burns, D. M.; Andemichael, Y. W.; Yemane, W. Org. Lett. 2000, 2, 3901. (d) Jullian, V.; Quirion, J.-C.; Husson, H.-P. Eur. J. Org. Chem. 2000, 1319. (e) Taniyama, D.: Hasegawa, M.; Tomioka, K. Tetrahedron: Asymmetry 1999, 10, 221. (f) Huber, I. M. P.; Seebach, D. Helv. Chim. Acta 1987, 70, 1944.
    • (2001) Synthesis , pp. 1513
    • Spengler, J.1    Schedel, H.2    Sieler, J.3    Quaedflieg, P.J.L.M.4    Broxterman, Q.B.5    Duchateau, A.L.L.6    Barger, K.7
  • 6
    • 0035808876 scopus 로고    scopus 로고
    • For recent examples see: (a) Spengler, J.; Schedel, H.; Sieler, J.; Quaedflieg, P. J. L. M.; Broxterman, Q. B.; Duchateau, A. L. L.; Barger, K. Synthesis 2001, 1513. (b) Meziane, M. A. A.; Royer, S.; Bazureau, J. P. Tetrahedron Lett. 2001, 42, 1017. (c) Davis, F. A.; Mohanty, P. K.; Burns, D. M.; Andemichael, Y. W.; Yemane, W. Org. Lett. 2000, 2, 3901. (d) Jullian, V.; Quirion, J.-C.; Husson, H.-P. Eur. J. Org. Chem. 2000, 1319. (e) Taniyama, D.: Hasegawa, M.; Tomioka, K. Tetrahedron: Asymmetry 1999, 10, 221. (f) Huber, I. M. P.; Seebach, D. Helv. Chim. Acta 1987, 70, 1944.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 1017
    • Meziane, M.A.A.1    Royer, S.2    Bazureau, J.P.3
  • 7
    • 0034736354 scopus 로고    scopus 로고
    • For recent examples see: (a) Spengler, J.; Schedel, H.; Sieler, J.; Quaedflieg, P. J. L. M.; Broxterman, Q. B.; Duchateau, A. L. L.; Barger, K. Synthesis 2001, 1513. (b) Meziane, M. A. A.; Royer, S.; Bazureau, J. P. Tetrahedron Lett. 2001, 42, 1017. (c) Davis, F. A.; Mohanty, P. K.; Burns, D. M.; Andemichael, Y. W.; Yemane, W. Org. Lett. 2000, 2, 3901. (d) Jullian, V.; Quirion, J.-C.; Husson, H.-P. Eur. J. Org. Chem. 2000, 1319. (e) Taniyama, D.: Hasegawa, M.; Tomioka, K. Tetrahedron: Asymmetry 1999, 10, 221. (f) Huber, I. M. P.; Seebach, D. Helv. Chim. Acta 1987, 70, 1944.
    • (2000) Org. Lett. , vol.2 , pp. 3901
    • Davis, F.A.1    Mohanty, P.K.2    Burns, D.M.3    Andemichael, Y.W.4    Yemane, W.5
  • 8
    • 0034009842 scopus 로고    scopus 로고
    • For recent examples see: (a) Spengler, J.; Schedel, H.; Sieler, J.; Quaedflieg, P. J. L. M.; Broxterman, Q. B.; Duchateau, A. L. L.; Barger, K. Synthesis 2001, 1513. (b) Meziane, M. A. A.; Royer, S.; Bazureau, J. P. Tetrahedron Lett. 2001, 42, 1017. (c) Davis, F. A.; Mohanty, P. K.; Burns, D. M.; Andemichael, Y. W.; Yemane, W. Org. Lett. 2000, 2, 3901. (d) Jullian, V.; Quirion, J.-C.; Husson, H.-P. Eur. J. Org. Chem. 2000, 1319. (e) Taniyama, D.: Hasegawa, M.; Tomioka, K. Tetrahedron: Asymmetry 1999, 10, 221. (f) Huber, I. M. P.; Seebach, D. Helv. Chim. Acta 1987, 70, 1944.
    • (2000) Eur. J. Org. Chem. , pp. 1319
    • Jullian, V.1    Quirion, J.-C.2    Husson, H.-P.3
  • 9
    • 0033613892 scopus 로고    scopus 로고
    • For recent examples see: (a) Spengler, J.; Schedel, H.; Sieler, J.; Quaedflieg, P. J. L. M.; Broxterman, Q. B.; Duchateau, A. L. L.; Barger, K. Synthesis 2001, 1513. (b) Meziane, M. A. A.; Royer, S.; Bazureau, J. P. Tetrahedron Lett. 2001, 42, 1017. (c) Davis, F. A.; Mohanty, P. K.; Burns, D. M.; Andemichael, Y. W.; Yemane, W. Org. Lett. 2000, 2, 3901. (d) Jullian, V.; Quirion, J.-C.; Husson, H.-P. Eur. J. Org. Chem. 2000, 1319. (e) Taniyama, D.: Hasegawa, M.; Tomioka, K. Tetrahedron: Asymmetry 1999, 10, 221. (f) Huber, I. M. P.; Seebach, D. Helv. Chim. Acta 1987, 70, 1944.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 221
    • Taniyama, D.1    Hasegawa, M.2    Tomioka, K.3
  • 10
    • 0023610480 scopus 로고
    • For recent examples see: (a) Spengler, J.; Schedel, H.; Sieler, J.; Quaedflieg, P. J. L. M.; Broxterman, Q. B.; Duchateau, A. L. L.; Barger, K. Synthesis 2001, 1513. (b) Meziane, M. A. A.; Royer, S.; Bazureau, J. P. Tetrahedron Lett. 2001, 42, 1017. (c) Davis, F. A.; Mohanty, P. K.; Burns, D. M.; Andemichael, Y. W.; Yemane, W. Org. Lett. 2000, 2, 3901. (d) Jullian, V.; Quirion, J.-C.; Husson, H.-P. Eur. J. Org. Chem. 2000, 1319. (e) Taniyama, D.: Hasegawa, M.; Tomioka, K. Tetrahedron: Asymmetry 1999, 10, 221. (f) Huber, I. M. P.; Seebach, D. Helv. Chim. Acta 1987, 70, 1944.
    • (1987) Helv. Chim. Acta , vol.70 , pp. 1944
    • Huber, I.M.P.1    Seebach, D.2
  • 11
    • 0035843415 scopus 로고    scopus 로고
    • For recent examples of excellent methods for preparation of quaternary tetrahydroisoquinoline-3-carboxylic acid derivatives see: (a) Alezra, V.; Bonin, M.; Micouin, L.; Husson, H.-P. Tetrahedron Lett. 2001, 42, 2111. (b) Ooi, T.; Takeuti, M.; Moruoka, K. Synthesis 2001, 1716.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 2111
    • Alezra, V.1    Bonin, M.2    Micouin, L.3    Husson, H.-P.4
  • 12
    • 0035843415 scopus 로고    scopus 로고
    • For recent examples of excellent methods for preparation of quaternary tetrahydroisoquinoline-3-carboxylic acid derivatives see: (a) Alezra, V.; Bonin, M.; Micouin, L.; Husson, H.-P. Tetrahedron Lett. 2001, 42, 2111. (b) Ooi, T.; Takeuti, M.; Moruoka, K. Synthesis 2001, 1716.
    • (2001) Synthesis , pp. 1716
    • Ooi, T.1    Takeuti, M.2    Moruoka, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.