메뉴 건너뛰기




Volumn 55, Issue 10, 2016, Pages 3455-3458

Catalytic SN2′- and Enantioselective Allylic Substitution with a Diborylmethane Reagent and Application in Synthesis

Author keywords

allylic substitution; boron; copper; enantioselective synthesis; N heterocyclic carbenes

Indexed keywords

ALLYLATION; BORON; CHEMICAL REACTIONS; COPPER; ENANTIOSELECTIVITY; ORGANIC COMPOUNDS; SUBSTITUTION REACTIONS;

EID: 84960812580     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201600309     Document Type: Article
Times cited : (113)

References (62)
  • 3
    • 33748541824 scopus 로고    scopus 로고
    • Angew. Chem. 2005, 117, 4509-4513;
    • (2005) Angew. Chem. , vol.117 , pp. 4509-4513
  • 7
    • 85192424635 scopus 로고    scopus 로고
    • For a recent review regarding applications of catalytic EAS reactions to natural product synthesis, see:, in (Eds.: A. Alexakis, N. Krause, S. Woodward), Wiley-VCH, Weinheim
    • For a recent review regarding applications of catalytic EAS reactions to natural product synthesis, see:, B. C. Calvo, J. Buter A. J. Minnaard, in Copper-Catalyzed Asymmetric Synthesis (Eds.:, A. Alexakis, N. Krause, S. Woodward,), Wiley-VCH, Weinheim, 2014, pp. 373-447.
    • (2014) Copper-Catalyzed Asymmetric Synthesis , pp. 373-447
    • Calvo, B.C.1    Minnaard, J.B.A.J.2
  • 11
    • 84921719817 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 5054-5058.
    • (2014) Angew. Chem. , vol.126 , pp. 5054-5058
  • 14
    • 84859554465 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 8815-8818;
    • (2011) Angew. Chem. , vol.123 , pp. 8815-8818
  • 16
    • 84877707173 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 6717-6721;
    • (2012) Angew. Chem. , vol.124 , pp. 6717-6721
  • 30
    • 17644389731 scopus 로고    scopus 로고
    • Angew. Chem. 2004, 116, 2480-2482;
    • (2004) Angew. Chem. , vol.116 , pp. 2480-2482
  • 32
    • 84957442364 scopus 로고    scopus 로고
    • While this manuscript was being prepared, a report appeared regarding related non-enantioselective processes with allylic chlorides promoted by achiral NHC-Cu complexes; see
    • While this manuscript was being prepared, a report appeared regarding related non-enantioselective processes with allylic chlorides promoted by achiral NHC-Cu complexes; see:, J. Kim, S. Park, J. Park, S. H. Cho, Angew. Chem. Int. Ed. 2016, 55, 1498-1501;
    • (2016) Angew. Chem. Int. Ed. , vol.55 , pp. 1498-1501
    • Kim, J.1    Park, S.2    Park, J.3    Cho, S.H.4
  • 33
    • 84977944547 scopus 로고    scopus 로고
    • Angew. Chem. 2016, 128, 1520-1523.
    • (2016) Angew. Chem. , vol.128 , pp. 1520-1523
  • 45
    • 84977970427 scopus 로고    scopus 로고
    • Angew. Chem. 2015, 127, 14347-14351.
    • (2015) Angew. Chem. , vol.127 , pp. 14347-14351
  • 50
    • 70349267328 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 7468-7472.
    • (2008) Angew. Chem. , vol.120 , pp. 7468-7472
  • 57
    • 0006160669 scopus 로고
    • See the Supporting Information for details
    • Angew. Chem. 1993, 105, 1095-1097). See the Supporting Information for details.
    • (1993) Angew. Chem. , vol.105 , pp. 1095-1097
  • 60
    • 0000397168 scopus 로고    scopus 로고
    • Angew. Chem. 2001, 113, 4676-4701.
    • (2001) Angew. Chem. , vol.113 , pp. 4676-4701
  • 61
    • 79956089533 scopus 로고    scopus 로고
    • for a review on oxa-Michael processes, see
    • K. Lee, H. Kim, J. Hong, Org. Lett. 2011, 13, 2722-2725; for a review on oxa-Michael processes, see:
    • (2011) Org. Lett. , vol.13 , pp. 2722-2725
    • Lee, K.1    Kim, H.2    Hong, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.