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Volumn 65, Issue 2, 2009, Pages 456-460

Triphenylphosphine dibromide: a simple one-pot esterification reagent

Author keywords

[No Author keywords available]

Indexed keywords

ACYLOXYALKOXYPHOSPHORANE; ALCOHOL; ALIPHATIC CARBOXYLIC ACID; BASE; CARBOXYLIC ACID; ESTER; PHOSPHORANE DERIVATIVE; TRIPHENYLPHOSPHINE; TRIPHENYLPHOSPHINE DIBROMIDE; UNCLASSIFIED DRUG;

EID: 56949094909     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.10.062     Document Type: Article
Times cited : (25)

References (67)
  • 12
    • 56949102440 scopus 로고    scopus 로고
    • Deng, L.; Hang, J.; Tang, L. US patent 2003/0166963 A1, 2003.
    • Deng, L.; Hang, J.; Tang, L. US patent 2003/0166963 A1, 2003.
  • 14
    • 56949092555 scopus 로고    scopus 로고
    • note
    • 3 instead of 5 led to no detectable loss in the optical purity of 7.
  • 41
    • 0000414496 scopus 로고
    • Beak P., et al. (Ed), John Wiley & Sons,, New York, NY
    • Hughes D.L. In: Beak P., et al. (Ed). Organic Reactions Vol. 42 (1992), John Wiley & Sons,, New York, NY 335-656
    • (1992) Organic Reactions , vol.42 , pp. 335-656
    • Hughes, D.L.1
  • 43
    • 56949089240 scopus 로고    scopus 로고
    • For other examples of Mitsunobu reactions proceeding with retention of the alcohol stereogenic center, see:
    • For other examples of Mitsunobu reactions proceeding with retention of the alcohol stereogenic center, see:
  • 53
    • 56949090758 scopus 로고    scopus 로고
    • Kelly, J. W. Ph.D. Dissertation; University of North Carolina at Chapel Hill: Chapel Hill, NC, 1986.
    • Kelly, J. W. Ph.D. Dissertation; University of North Carolina at Chapel Hill: Chapel Hill, NC, 1986.
  • 61
    • 56949099650 scopus 로고    scopus 로고
    • note
    • A similar adverse steric interaction may exist after Berry psuedorotation of 14 to 14′ prior to intramolecular attack to give the esterified product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.