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Volumn 62, Issue 23, 1997, Pages 7926-7936

Lewis Acid Catalysis in the Oxidative Cycloaddition of Thiophenes

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EID: 0000314020     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961985z     Document Type: Article
Times cited : (68)

References (68)
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    • note
    • The X-ray analysis of 3 has been performed before; see ref 12. In the case, however, 3 was formed in the uncatalyzed reaction.
  • 40
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    • note
    • Although in most Diels-Alder reactions of cyclic dienes the cycloadducts are formed predominantly by endo-addition, there have been many reports of mixtures of endo/exo-products.
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    • This has been discussed in: (a) Houk, K. N.; Strozier, R. W. J. Am. Chem. Soc. 1973, 95, 4904-4096. (b) Alston, P. V.; Ottenbrite, R. M. J. Org. Chem. 1975, 40, 1111-1116. (c) Birney, D. M.; Houk, K. N. J. Am. Chem. Soc. 1990, 112, 4127-4133.
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    • This has been discussed in: (a) Houk, K. N.; Strozier, R. W. J. Am. Chem. Soc. 1973, 95, 4904-4096. (b) Alston, P. V.; Ottenbrite, R. M. J. Org. Chem. 1975, 40, 1111-1116. (c) Birney, D. M.; Houk, K. N. J. Am. Chem. Soc. 1990, 112, 4127-4133.
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    • University of Göttingen
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    • note
    • The author has deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystal- lographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.