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Volumn 11, Issue 20, 2009, Pages 4576-4579

Readily prepared 3-Chloro-1 -(phenylthio)propene, a versatile three-carbon annulating agent

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EID: 70349925292     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901818j     Document Type: Article
Times cited : (15)

References (27)
  • 11
    • 0036499897 scopus 로고    scopus 로고
    • Terminal alkenes readily undergo cyclization by intramolecular carbolthiation to generated cyclopenylmethyllithiums. Reviews
    • Terminal alkenes readily undergo cyclization by intramolecular carbolthiation to generated cyclopenylmethyllithiums. Reviews: (a) Mealy, M. J.; Bailey, W. F. J. Organomet. Chem. 2002, 646, 59-67.
    • (2002) J. Organomet. Chem. , vol.646 , pp. 59-67
    • Mealy, M.J.1    Bailey, W.F.2
  • 18
    • 70349925443 scopus 로고    scopus 로고
    • Crystallographic data of 10 (CCDC 278769) can be obtained free of charge from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk.
    • Crystallographic data of 10 (CCDC 278769) can be obtained free of charge from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk.
  • 21
    • 70349921142 scopus 로고    scopus 로고
    • Crystallographic data of 21 (CCDC 739965) can be obtained free of charge via from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk
    • Crystallographic data of 21 (CCDC 739965) can be obtained free of charge via from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk.
  • 22
    • 0343016503 scopus 로고
    • The potassium salts of several phenols were reported to undergo ortho-allylation in the presence of various allylic halides and catalytic amounts of zinc chloride but neither other products nor a mechanism were discussed
    • The potassium salts of several phenols were reported to undergo ortho-allylation in the presence of various allylic halides and catalytic amounts of zinc chloride but neither other products nor a mechanism were discussed: Bigi, F.; Casiraghi, G.; Casnati, G.; Sartori, G. Synthesis 1981, 310-312.
    • (1981) Synthesis , pp. 310-312
    • Bigi, F.1    Casiraghi, G.2    Casnati, G.3    Sartori, G.4
  • 23
    • 0020851963 scopus 로고
    • However, a 6-member ring transition state can be surmised from a subsequent review by some of the same authors
    • However, a 6-member ring transition state can be surmised from a subsequent review by some of the same authors: Casnati, G.; Casiraghi, G.; Pochini, A.; Sartori, G.; Ungaro, R. Pure Appl. Chem. 1983, 55, 1677-1688.
    • (1983) Pure Appl. Chem. , vol.55 , pp. 1677-1688
    • Casnati, G.1    Casiraghi, G.2    Pochini, A.3    Sartori, G.4    Ungaro, R.5
  • 24
    • 37049106180 scopus 로고
    • The replacement of the phenylthio group of 23 by allyl, Cl, and F as well as its oxidation to a sulfoxide is recorded in the literature but curiously no synthesis of 23 appears.
    • The replacement of the phenylthio group of 23 by allyl, Cl, and F as well as its oxidation to a sulfoxide is recorded in the literature but curiously no synthesis of 23 appears. Nishiyama, H.; Narimatsu, S.; Sakuta, K.; Itoh, K. J. Chem. Soc., Chem. Commun. 1982, 459-460.
    • (1982) J. Chem. Soc., Chem. Commun. , pp. 459-460
    • Nishiyama, H.1    Narimatsu, S.2    Sakuta, K.3    Itoh, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.