메뉴 건너뛰기




Volumn 358, Issue 4, 2016, Pages 555-560

Planar-Chiral Cyclopentadienyl-Ruthenium-Catalyzed Regio- and Enantioselective Asymmetric Allylic Alkylation of Silyl Enolates under Unusually Mild Conditions

Author keywords

asymmetric allylic substitution; cyclopentadienyl ruthenium; enantioselective catalysis; planar chirality; silyl enolates

Indexed keywords


EID: 84958742245     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201500970     Document Type: Article
Times cited : (26)

References (92)
  • 8
    • 33746302230 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 2466-2469;
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2466-2469
  • 12
    • 0038249086 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 2054-2056;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2054-2056
  • 17
    • 0037014083 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 1929-1932;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1929-1932
  • 22
    • 0034596811 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3494-3497;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3494-3497
  • 27
    • 84937738181 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2015, 54, 9120-9123;
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 9120-9123
  • 32
    • 0037119732 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 3492-3495.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3492-3495
  • 35
    • 53549086402 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1741-1744;
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1741-1744
  • 49
    • 8544252475 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 5590-5614;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5590-5614
  • 51
    • 84882837030 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 9086-9096;
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 9086-9096
  • 53
    • 84882976844 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 9109-9118.
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 9109-9118
  • 57
    • 84905822679 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2014, 53, 8691-8695;
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 8691-8695
  • 59
    • 84911489586 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2014, 53, 12172-12176;
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 12172-12176
  • 62
    • 0037087753 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 1059-1061;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1059-1061
  • 69
    • 34250868476 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 2082-2085;
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 2082-2085
  • 73
    • 79955672250 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 4649-4653;
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 4649-4653
  • 81
    • 39849107380 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1454-1457;
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1454-1457
  • 84
    • 79956123740 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 5197-5199;
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5197-5199
  • 86
    • 84876566746 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 4897-4901;
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 4897-4901
  • 88
    • 84958797974 scopus 로고    scopus 로고
    • 3=Me) as nucleophiles were carried out in the reaction systems, both of the nucleophiles showed lower reactivity (yields <10%) than 3a
    • 3=Me) as nucleophiles were carried out in the reaction systems, both of the nucleophiles showed lower reactivity (yields <10%) than 3a.
  • 92
    • 84958797975 scopus 로고    scopus 로고
    • The enantioselectivity of 4aa is 87% ee, which is in agreement with our proposed reaction mechanism
    • The enantioselectivity of 4aa is 87% ee, which is in agreement with our proposed reaction mechanism.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.