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Volumn 131, Issue 20, 2009, Pages 6916-6917

Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor

Author keywords

[No Author keywords available]

Indexed keywords

2-PROPANOL; [CARBONYL; ALCOHOL OXIDATION; ALIPHATIC ALDEHYDES; ALLENES; ALLYL ACETATE; ALLYL COMPLEXES; ALLYLMETALS; C-C BONDS; CARBONYL ADDITION; DIMETHYLALLENE; ENANTIOSELECTIVE; HYDRIDE ELIMINATION; HYDROMETALATION; ISOLATED YIELD; ISOTOPIC LABELING; NITROBENZOIC ACIDS; OXIDATION LEVEL; PRENYLATION; SEGPHOS; TRANSFER HYDROGENATIONS;

EID: 70149095459     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja902437k     Document Type: Article
Times cited : (128)

References (33)
  • 1
    • 33846995439 scopus 로고    scopus 로고
    • For selected reviews of C-C bond-forming hydrogenation and transfer hydrogenation, see: (a) Ngai, M.-Y.; Kong, J. R.; Krische, M. J. J. Org. Chem 2007, 72, 1063.
    • (2007) J. Org. Chem , vol.72 , pp. 1063
    • Ngai, M.-Y.1    Kong, J.R.2    Krische, M.J.3
  • 4
    • 33845585619 scopus 로고    scopus 로고
    • For selected examples of carbonyl and imine vinylation employing alkynes as vinyl donors under hydrogenation conditions, see: (a) Kong, J.-R.; Krische, M. J. J. Am. Chem. Soc. 2006, 128, 16040.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 16040
    • Kong, J.-R.1    Krische, M.J.2
  • 9
    • 35548993714 scopus 로고    scopus 로고
    • For carbonyl allylation via iridium-catalyzed hydrogenative and transfer hydrogenative coupling of dienes, alienes, and allyl acetates, see: (a) Skucas, E.; Bower, J. F.; Krische, M. J. J. Am. Chem. Soc. 2007, 129, 12678.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12678
    • Skucas, E.1    Bower, J.F.2    Krische, M.J.3
  • 15
    • 43949117421 scopus 로고    scopus 로고
    • For carbonyl allylation via ruthenium-catalyzed transfer hydrogenative coupling of dienes and alienes, see: (a) Shibahara, F.; Bower, J. F.; Krische, M. J. J. Am Chem. Soc. 2008, 130, 6338.
    • (2008) J. Am Chem. Soc. , vol.130 , pp. 6338
    • Shibahara, F.1    Bower, J.F.2    Krische, M.J.3
  • 19
    • 60949105307 scopus 로고    scopus 로고
    • For a recent review covering intermolecular aldol and Mannich addition via rhodium-catalyzed hydrogenative coupling of enones, see: Han, S. B.; Hassan, A.; Krische, M. J. Synthesis 2008, 2669.
    • (2008) Synthesis , pp. 2669
    • Han, S.B.1    Hassan, A.2    Krische, M.J.3
  • 20
    • 0034597504 scopus 로고    scopus 로고
    • Palladium-catalyzed reductive coupling of 1,1-dimethylallene to carbonyl compounds mediated by SnCl2 provides racemic products of reverse prenylation. See: Chang, H.-M.; Cheng, C.-H. Org. Lett. 2000, 2, 3439.
    • (2000) Org. Lett. , vol.2 , pp. 3439
    • Chang, H.-M.1    Cheng, C.-H.2
  • 21
    • 0001665126 scopus 로고
    • For enantioselective carbonyl reverse prenylation employing allylboron reagents, see: (a) Brown, H. C.; Jadhav, P. K Tetrahedron Lett. 1984, 25, 1215.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 1215
    • Brown, H.C.1    Jadhav, P.K.2
  • 23
    • 0033601395 scopus 로고    scopus 로고
    • For enantioselective carbonyl reverse prenylation employing allylindium reagents, see: (a) Loh, T.-P.; Zhou, J. R.; Li, X.-R. Tetrahedron Lett. 1999, 40, 9333.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 9333
    • Loh, T.-P.1    Zhou, J.R.2    Li, X.-R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.