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Volumn 15, Issue 8, 2013, Pages 1934-1937

A chemoenzymatic total synthesis of the protoilludane aryl ester (+)-armillarivin

Author keywords

[No Author keywords available]

Indexed keywords

ARMILLARIVIN; BIOLOGICAL PRODUCT; CYCLOPENTANE DERIVATIVE; CYCLOPENTENONE; ESTER; PROTOILLUDANE; SESQUITERPENE;

EID: 84876520284     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol400583c     Document Type: Article
Times cited : (37)

References (24)
  • 14
    • 0000290698 scopus 로고
    • This protocol is based on one first described by Ma and Bobbitt
    • This protocol is based on one first described by Ma and Bobbitt: Ma, Z.; Bobbitt, J. M. J. Org. Chem. 1991, 56, 6110
    • (1991) J. Org. Chem. , vol.56 , pp. 6110
    • Ma, Z.1    Bobbitt, J.M.2
  • 21
    • 84871796862 scopus 로고    scopus 로고
    • For a very recent review of the oxa-di-π-methane rearrangement, see: Rao, V. J.; Srinivas, K. In CRC Handbook of Organic Photochemistry and Photobiology, 3 rd ed; Griesbeck, A. G.; Oelgemöller, M.; Ghetti, F., Eds.; CRC Press: Boca Raton, FL, 2012; Chapter 22, pp 527-548.
    • (2012) CRC Handbook of Organic Photochemistry and Photobiology , pp. 527-548
    • Rao, V.J.1    Srinivas, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.