메뉴 건너뛰기




Volumn 38, Issue 1-2, 1999, Pages 110-113

Palladium-mediated dynamic kinetic resolution: Stereoselective synthesis of vicinal diamines

Author keywords

Allyl complexes; Aminations; Diamines; Palladium; Stereoselective synthesis

Indexed keywords

DIAMINE; PALLADIUM;

EID: 0033555202     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19990115)38:1/2<110::AID-ANIE110>3.0.CO;2-L     Document Type: Article
Times cited : (32)

References (34)
  • 1
    • 0000276556 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming, M. F. Semmelhock), Pergamon, Oxford
    • For recent reviews, see a) S. A. Godleski in Comprehensive Organic Synthesis, Vol. 4 (Eds.: B. M. Trost, I. Fleming, M. F. Semmelhock), Pergamon, Oxford, 1991, p. 585;
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 585
    • Godleski, S.A.1
  • 2
    • 0003872342 scopus 로고
    • (Ed.: M. Schlosser), Wiley, New York
    • b) L. Hegedus in Organometallics in Synthesis (Ed.: M. Schlosser), Wiley, New York, 1994; pp. 385-459;
    • (1994) Organometallics in Synthesis , pp. 385-459
    • Hegedus, L.1
  • 4
    • 0001064399 scopus 로고
    • For reviews on asymmetric palladium-catalyzed allylic substitutions, see a) O. Reiser, Angew. Chem. 1993, 105, 576; Angew. Chem. Int. Ed. Engl. 1993, 32, 547;
    • (1993) Angew. Chem. , vol.105 , pp. 576
    • Reiser, O.1
  • 5
    • 33748245787 scopus 로고
    • For reviews on asymmetric palladium-catalyzed allylic substitutions, see a) O. Reiser, Angew. Chem. 1993, 105, 576; Angew. Chem. Int. Ed. Engl. 1993, 32, 547;
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 547
  • 11
    • 0010242966 scopus 로고    scopus 로고
    • Asymmetry in the allylic substrate adjacent to the π-allyl complex has only been investigated in the context of intramolecular cyclizations or intermolecular reactions with cyclic substrates. For recent examples, see a) J. Pohlmann, C. Sabater, H. M. R. Hoffmann, Angew. Chem. 1998, 110, 656; Angew. Chem. Int. Ed. 1998, 37, 633;
    • (1998) Angew. Chem. , vol.110 , pp. 656
    • Pohlmann, J.1    Sabater, C.2    Hoffmann, H.M.R.3
  • 12
    • 0031949287 scopus 로고    scopus 로고
    • Asymmetry in the allylic substrate adjacent to the π-allyl complex has only been investigated in the context of intramolecular cyclizations or intermolecular reactions with cyclic substrates. For recent examples, see a) J. Pohlmann, C. Sabater, H. M. R. Hoffmann, Angew. Chem. 1998, 110, 656; Angew. Chem. Int. Ed. 1998, 37, 633;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 633
  • 15
    • 0026418434 scopus 로고
    • d) B. M. Trost, Science 1991, 254, 1471;
    • (1991) Science , vol.254 , pp. 1471
    • Trost, B.M.1
  • 17
    • 0000467795 scopus 로고
    • f) B. M. Trost, Angew. Chem. 1989, 101, 1199; Angew. Chem. Int. Ed. Engl. 1989, 28, 1173.
    • (1989) Angew. Chem. , vol.101 , pp. 1199
    • Trost, B.M.1
  • 18
    • 84990085666 scopus 로고
    • f) B. M. Trost, Angew. Chem. 1989, 101, 1199; Angew. Chem. Int. Ed. Engl. 1989, 28, 1173.
    • (1989) Angew. Chem. Int. Ed. Engl. , vol.28 , pp. 1173
  • 22
    • 0001651521 scopus 로고    scopus 로고
    • for recent examples, see b) R. Prétȯt, A. Pfaltz, Angew. Chem. 1998, 110, 337; Angew. Chem. Int. Ed. 1998, 37, 323;
    • (1998) Angew. Chem. , vol.110 , pp. 337
    • Prétot, R.1    Pfaltz, A.2
  • 23
    • 0032536559 scopus 로고    scopus 로고
    • for recent examples, see b) R. Prétȯt, A. Pfaltz, Angew. Chem. 1998, 110, 337; Angew. Chem. Int. Ed. 1998, 37, 323;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 323
  • 28
    • 0345143377 scopus 로고    scopus 로고
    • note
    • 6] followed by a Mitsunobu reaction with phthalimide afforded a diamine derviative which correlated spectroscopically to the minor isomer 8b.
  • 31
  • 32
    • 33748222603 scopus 로고
    • c) A. Togni, L. M. Venanzi, Angew. Chem. 1994, 106, 517; Angew. Chem. Int. Ed. Engl. 1994, 33, 497.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 497


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.