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Volumn 70, Issue 27-28, 2014, Pages 4089-4093

Synthetic studies toward the citrinadins: Enantioselective preparation of an advanced spirooxindole intermediate

Author keywords

Citrinadin; Heck reaction; Natural product; Spirooxindole; synthesis

Indexed keywords

ACID; ALCOHOL; AMIDE; BROMINE DERIVATIVE; CITRINADIN A; CITRINADIN B; DIBROMIDE; ENONE; ESTER; INDOLE DERIVATIVE; NATURAL PRODUCT; SILANE DERIVATIVE; SPIROOXINDOLE; UNCLASSIFIED DRUG;

EID: 84901351708     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.02.046     Document Type: Article
Times cited : (14)

References (11)
  • 5
    • 40949124014 scopus 로고    scopus 로고
    • This structural revision brings the structures of citrinadins A and B in closer alignment to those assigned crystallographically to the similar oxindole-containing alkaloids PF1270A-C, see
    • This structural revision brings the structures of citrinadins A and B in closer alignment to those assigned crystallographically to the similar oxindole-containing alkaloids PF1270A-C, see N. Kushida, N. Watanabe, T. Okuda, F. Yokoyama, Y. Gyobu, and T. Yaguchi J. Antibiot. 60 2007 667 673
    • (2007) J. Antibiot. , vol.60 , pp. 667-673
    • Kushida, N.1    Watanabe, N.2    Okuda, T.3    Yokoyama, F.4    Gyobu, Y.5    Yaguchi, T.6
  • 11
    • 33947085552 scopus 로고
    • The stereochemical outcome of this reaction was assigned as illustrated based on the model developed by Corey. This assignment was supported by reduction of 19 employing the (R)-oxazaborolidine and comparison of the derived enantiomers via their corresponding Mosher esters, see
    • The stereochemical outcome of this reaction was assigned as illustrated based on the model developed by Corey. This assignment was supported by reduction of 19 employing the (R)-oxazaborolidine and comparison of the derived enantiomers via their corresponding Mosher esters, see: J.A. Dale, and H.S. Mosher J. Am. Chem. Soc. 95 1973 512 519
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 512-519
    • Dale, J.A.1    Mosher, H.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.