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Volumn 13, Issue 4, 2011, Pages 740-743

Cyclopropenium-activated cyclodehydration of diols

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[No Author keywords available]

Indexed keywords


EID: 79951599208     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol102980t     Document Type: Article
Times cited : (58)

References (14)
  • 6
    • 0038640173 scopus 로고    scopus 로고
    • For a review on cyclopropenium ions, see
    • For a review on cyclopropenium ions, see: Komatsu, K.; Kitagawa, T. Chem. Rev. 2003, 103, 1371
    • (2003) Chem. Rev. , vol.103 , pp. 1371
    • Komatsu, K.1    Kitagawa, T.2
  • 8
    • 11844292026 scopus 로고    scopus 로고
    • See the following selected papers for diol cyclodehydrations using: Platinium:,. Triphenylphosphine
    • See the following selected papers for diol cyclodehydrations using: Platinium: Shibata, T.; Fujiwara, R.; Ueno, Y. Synlett, 2005, 152. Triphenylphosphine
    • (2005) Synlett , vol.152
    • Shibata, T.1    Fujiwara, R.2    Ueno, Y.3
  • 12
    • 0037625717 scopus 로고    scopus 로고
    • For a review on cyclopropenone acetals, see
    • For a review on cyclopropenone acetals, see: Nakamura, M.; Isobe, H.; Nakamura, E. Chem. Rev. 2003, 103, 1295
    • (2003) Chem. Rev. , vol.103 , pp. 1295
    • Nakamura, M.1    Isobe, H.2    Nakamura, E.3
  • 14
    • 79951625150 scopus 로고    scopus 로고
    • Efforts to extend the current protocol to the formation of ring sizes smaller than 5 or greater than 6 have not yet been successful.
    • Efforts to extend the current protocol to the formation of ring sizes smaller than 5 or greater than 6 have not yet been successful.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.