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Volumn 13, Issue 10, 2011, Pages 2594-2597

Stereoselective synthesis of β-(hydroxymethylaryl/alkyl)-α- methylene-γ-butyrolactones

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA METHYLENE BUTYROLACTONE; ALPHA-METHYLENE GAMMA-BUTYROLACTONE; CHROMIUM; DRUG DERIVATIVE; FURAN DERIVATIVE; GAMMA BUTYROLACTONE; HYDROXYMATAIRESINOL; LACTONE; LIGNAN; METHYLENOLACTOCIN; ZINC;

EID: 79956094858     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200711f     Document Type: Article
Times cited : (49)

References (38)
  • 9
    • 79956150730 scopus 로고    scopus 로고
    • During the course of our studies, a single example of this process involving zinc with 3 and a complex chiral aldehyde was reported in a patent:; CN 101481367
    • During the course of our studies, a single example of this process involving zinc with 3 and a complex chiral aldehyde was reported in a patent: Xu, X.; Yang, H.; Qiao, X.; Xie, L. CN 101481367, 2009
    • (2009)
    • Xu, X.1    Yang, H.2    Qiao, X.3    Xie, L.4
  • 10
    • 79956143193 scopus 로고    scopus 로고
    • Chem. Abstr., 2009, 151, 245843.
    • (2009) Chem. Abstr. , vol.151 , pp. 245843
  • 11
    • 67650351143 scopus 로고    scopus 로고
    • The reaction of zinc with 3 and formaldehyde has also been recently reported
    • The reaction of zinc with 3 and formaldehyde has also been recently reported: Yang, H. S.; Qiao, X. X.; Cui, Q.; Xu, X. H. Chin. Chem. Lett. 2009, 20, 1023-1024
    • (2009) Chin. Chem. Lett. , vol.20 , pp. 1023-1024
    • Yang, H.S.1    Qiao, X.X.2    Cui, Q.3    Xu, X.H.4
  • 14
    • 66049158938 scopus 로고    scopus 로고
    • Corrigendum.
    • Corrigendum: J. Nat. Prod. 2009, 72, 804.
    • (2009) J. Nat. Prod. , vol.72 , pp. 804
  • 15
    • 79956147328 scopus 로고    scopus 로고
    • The stereochemistries of 1 and 2 are currently not known with certainty.
    • The stereochemistries of 1 and 2 are currently not known with certainty.
  • 24
    • 79956080979 scopus 로고    scopus 로고
    • 4Cl.
    • 4Cl.
  • 26
    • 79956125039 scopus 로고    scopus 로고
    • See the Supporting Information for details.
    • See the Supporting Information for details.
  • 27
    • 79956121062 scopus 로고    scopus 로고
    • For details of aldehyde preparation see the Supporting Information.
    • For details of aldehyde preparation see the Supporting Information.
  • 28
    • 0034295151 scopus 로고    scopus 로고
    • The spectral data were in full accord with the stereochemistry indicated in Table 2, entry 4, and also differed from the previously reported data for the diastereomeric MOM ether
    • The spectral data were in full accord with the stereochemistry indicated in Table 2, entry 4, and also differed from the previously reported data for the diastereomeric MOM ether: Yamauchi, S.; Yamamoto, N.; Kinoshita, Y. Biosci. Biotechnol. Biochem. 2000, 64, 2209-2215
    • (2000) Biosci. Biotechnol. Biochem. , vol.64 , pp. 2209-2215
    • Yamauchi, S.1    Yamamoto, N.2    Kinoshita, Y.3
  • 34
    • 34249336049 scopus 로고    scopus 로고
    • Allylation using the zinc conditions gave 5j in 79% yield (83:17 dr). The minor diastereomer was determined to be that previously reported (see the Supporting Information).
    • Hon, Y.-S.; Hsieh, C.-H.; Chen, H.-F. Synth. Commun. 2007, 37, 1635-1651 Allylation using the zinc conditions gave 5j in 79% yield (83:17 dr). The minor diastereomer was determined to be that previously reported (see the Supporting Information).
    • (2007) Synth. Commun. , vol.37 , pp. 1635-1651
    • Hon, Y.-S.1    Hsieh, C.-H.2    Chen, H.-F.3
  • 37
    • 79956095643 scopus 로고    scopus 로고
    • Submitting primary alcohol 9 to the reaction conditions gave the same 4:96 mixture of 5k: 9 observed when starting with 5k.
    • Submitting primary alcohol 9 to the reaction conditions gave the same 4:96 mixture of 5k: 9 observed when starting with 5k.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.