메뉴 건너뛰기




Volumn 131, Issue 43, 2009, Pages 15624-15626

Enantioselective synthesis of 1,2,3-trisubstituted cyclopropanes using gem-dizinc reagents

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLIC ALCOHOL; CARBENOIDS; CHEMICAL EQUATIONS; CHIRAL LIGAND; CYCLOPROPANATION; CYCLOPROPANE DERIVATIVE; CYCLOPROPYL; DIASTEREOSELECTIVITIES; ENANTIO; ENANTIOSELECTIVE SYNTHESIS; HIGH YIELD; IN-SITU; SUZUKI-MIYAURA CROSS-COUPLING REACTION;

EID: 70350635633     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja906033g     Document Type: Article
Times cited : (54)

References (54)
  • 7
    • 0035828834 scopus 로고    scopus 로고
    • and references cited therein
    • (g) Donaldson, W. A. Tetrahedron 2001, 57, 8589, and references cited therein.
    • (2001) Tetrahedron , vol.57 , pp. 8589
    • Donaldson, W.A.1
  • 19
    • 25444443951 scopus 로고    scopus 로고
    • Another method leading to cis-substituted iodocyclopropanes was developed by Walsh and co-workers. See: (a)
    • Another method leading to cis-substituted iodocyclopropanes was developed by Walsh and co-workers. See: (a) Kim, H. Y.; Lurain, A. E.; García- García, P.; Carroll, P. J.; Walsh, P. J. J. Am. Chem. Soc. 2005, 127, 13138.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 13138
    • Kim, H.Y.1    Lurain, A.E.2    García- García, P.3    Carroll, P.J.4    Walsh, P.J.5
  • 28
    • 33845274756 scopus 로고    scopus 로고
    • For use of a chiral zinc carbenoid, see: (g)
    • For use of a chiral zinc carbenoid, see: (g) Voituriez, A.; Charette, A. B. Adv. Synth. Catal. 2006, 348, 2363.
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 2363
    • Voituriez, A.1    Charette, A.B.2
  • 31
    • 53549091021 scopus 로고    scopus 로고
    • For use of a catalytic ligand, see: (i)
    • For use of a catalytic ligand, see: (i) Shitama, H.; Katsuki, T. Angew. Chem., Int. Ed. 2008, 47, 2450.
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 2450
    • Shitama, H.1    Katsuki, T.2
  • 37
    • 70350645841 scopus 로고    scopus 로고
    • note
    • See the Supporting Information.
  • 41
  • 42
    • 70350634476 scopus 로고    scopus 로고
    • note
    • 2O) for 11a: δ 53.0.
  • 43
    • 34547444477 scopus 로고    scopus 로고
    • For recent examples of the utility of cyclopropyl boronic acids and esters, see: (a)
    • For recent examples of the utility of cyclopropyl boronic acids and esters, see: (a) Rubin, M.; Rubina, M.; Gevorgyan, V. Chem. Rev. 2007, 107, 3117.
    • (2007) Chem. Rev. , vol.107 , pp. 3117
    • Rubin, M.1    Rubina, M.2    Gevorgyan, V.3
  • 53
    • 33746190548 scopus 로고
    • For interactions between iodine and π systems, see
    • For interactions between iodine and π systems, see: Benesi, H. A.; Hildebrand, J. H. J. Am. Chem. Soc. 1949, 71, 2703.
    • (1949) J. Am. Chem. Soc. , vol.71 , pp. 2703
    • Benesi, H.A.1    Hildebrand, J.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.