메뉴 건너뛰기




Volumn 48, Issue 43, 2009, Pages 8129-8132

Synthesis of chiral tetrasubstituted alkenes by an asymmetric cascade reaction catalyzed cooperatively by cationic rhodium(I) and silver(I) complexes

Author keywords

Alkenes; Asymmetric catalysis; Cascade reactions; Helical chirality; Rhodium

Indexed keywords

ALKENES; ASYMMETRIC CATALYSIS; CASCADE REACTIONS; DIASTEREOSELECTIVE SYNTHESIS; ENANTIO; HELICAL CHIRALITY; HIGH ENANTIOSELECTIVITY; SILVER COMPLEXES;

EID: 70349970829     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200904024     Document Type: Article
Times cited : (54)

References (64)
  • 1
    • 70349969460 scopus 로고    scopus 로고
    • For recent reviews of cascade reactions, see
    • For recent reviews of cascade reactions, see
  • 5
    • 70349954697 scopus 로고    scopus 로고
    • For recent reviews of asymmetric cascade reactions, see
    • For recent reviews of asymmetric cascade reactions, see
  • 11
    • 70349941102 scopus 로고    scopus 로고
    • Recently, a novel domino synthesis of tetrasubstituted helical alkenes through C-H bond functionalization was reported; see
    • Recently, a novel domino synthesis of tetrasubstituted helical alkenes through C-H bond functionalization was reported; see
  • 14
    • 70349937832 scopus 로고    scopus 로고
    • For leading reference, see
    • For leading reference, see
  • 16
    • 70349975635 scopus 로고    scopus 로고
    • for reviews, see
    • for reviews, see
  • 22
    • 70349948772 scopus 로고    scopus 로고
    • For rhodium-catalyzed [4+2] annulations of 2-alkynylbenzalde- hydes with unsaturated compounds, see
    • For rhodium-catalyzed [4+2] annulations of 2-alkynylbenzalde- hydes with unsaturated compounds, see
  • 28
    • 70349956411 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 31
    • 70349948784 scopus 로고    scopus 로고
    • For examples, see
    • For examples, see
  • 38
    • 70349948782 scopus 로고    scopus 로고
    • For examples, see
    • For examples, see
  • 50
    • 70349954690 scopus 로고    scopus 로고
    • For rhodium-catalyzed cyclizations, see
    • For rhodium-catalyzed cyclizations, see
  • 53
    • 70349952029 scopus 로고    scopus 로고
    • I-catalyzed carbonyl alkyne metathesis, see
    • I-catalyzed carbonyl alkyne metathesis, see
  • 55
    • 70349957918 scopus 로고    scopus 로고
    • for RhI- catalyzed carbonyl alkyne metathesis, see
    • for RhI- catalyzed carbonyl alkyne metathesis, see
  • 57
    • 70349928554 scopus 로고    scopus 로고
    • For a rhodium-catalyzed enantioselective intramolecular hydro- acylation of ketones with aldehydes, see
    • For a rhodium-catalyzed enantioselective intramolecular hydro- acylation of ketones with aldehydes, see
  • 59
    • 70349959795 scopus 로고    scopus 로고
    • 3.
    • 3.
  • 61
    • 70349937824 scopus 로고    scopus 로고
    • Acyclic 1 2-dicarbonyl compounds, such as ?-ketoesters and 1 2- diketones, failed to react with 1b.
    • Acyclic 1 2-dicarbonyl compounds, such as ?-ketoesters and 1 2- diketones, failed to react with 1b.
  • 62
    • 70349939398 scopus 로고    scopus 로고
    • The absolute configuration of (-)-(E)-4dd was determined to be S by X-ray crystallographic analysis of the corresponding Z isomer.
    • The absolute configuration of (-)-(E)-4dd was determined to be S by X-ray crystallographic analysis of the corresponding Z isomer.
  • 63
    • 70349943723 scopus 로고    scopus 로고
    • CCDC 738708 (4aa), 738707 ((S)-(-)-(Z)-4dd), 738706 (4ha), and 738705 (4he) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 738708 (4aa), 738707 ((S)-(-)-(Z)-4dd), 738706 (4ha), and 738705 (4he) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 64
    • 70349937811 scopus 로고    scopus 로고
    • 2 solution of (Z)-4he.
    • 2 solution of (Z)-4he.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.