SCOPUS 정보 검색 플랫폼

Volumn 31, Issue 50, 1990, Pages 7315-7318

Synthesis of hydroisoindoles via intramolecular Diels-Alder reactions

a CNRS (France)

Author keywords

[No Author keywords available]

Indexed keywords

ISOINDOLE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL;

BETULACEAE;

EID: 0025678429 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)88553-6 Document Type: Article

Times cited : (2)

References (15)

1
- 0003360065
- The intramolecular Diels–Alder reaction: recent advances and synthetic applications
- For recent reviews see:
- (1984) Canadian Journal of Chemistry , vol.62 , pp. 183
- Fallis¹

5
- 0000498745
- Synthetic control by internal interaction. The intramolecular Diels-Alder reactions of furan derivatives and .ALPHA.,.BETA.-unsaturated amides.
- (1983) Bulletin of the Chemical Society of Japan , vol.56 , pp. 1107
- Takebayashi¹ Iwasawa² Mukaiyama³

6
- 33845551047
- (1983) J. Org. Chem. , vol.48 , pp. 5170
- Martin¹ Williamson² Gist³ Smith⁴

8
- 37049077598
- Synthesis of hydroisoindoles via intramolecular Diels?Alder reactions of functionalised amido trienes
- (1989) Journal of the Chemical Society, Perkin Transactions 1 , pp. 997
- Mellor¹ Wagland²

10
- 33845553504
- (1982) J. Amer. Chem. Soc. , vol.104 , pp. 5719
- Pyne¹ Hensel² Fuchs³

12
- 33845470159
- (1984) J. Amer. Chem. Soc. , vol.106 , pp. 1133
- Yoshioka¹ Nakai² Ohno³

14
- 0000449208
- Chlorocyanation of barrelenes as a route to 1-cyanosemibullvalenes. Convenient introduction of an efficient .pi.-electron acceptor substituent and its influence on the Cope equilibrium
- (1976) Journal of the American Chemical Society , vol.98 , pp. 2910
- Overman¹

15
- 84918597319
- 3, δ ppm)3 ct 1.78 (m, 2H), 2.18 (m, 2H), 2.3 (m, 1H), 2.95 (m, 1H), 4.18 (m, 2H), 5.84 (d, 1H), 5.62 (m, 1H), 5.84 (m, 1H), 7.26 (m, 5H)3 tc 1.5–2.25 (m, 5H), 2.64–2.85 (m, 1H), 3.45–3.8 (m, 1H), 4.5–4.65 (m, 1H), 5.25 (d, 1H), 5.65–5.9 (m, 2H), 7.1–7.4 (m, 5H)3 tt 1.62 (m, 1H), 1.75 (m, 1H), 1.92 (m, 1H), 2.26 (m, 2H), 2.44 (m, 1H), 3.51 (m, 1H), 4.54 (m, 1H), 4.63 (m, 1H), 5.78 (m, 2H), 7.29 (m, 5H)3 cc 1.5–2.2 (m, 4H), 2.5–2.65 (m, 1H), 2.75–2.9 (m, 1H), 4.55–4.7 (m, 2H), 5.4 (d, 1H), 5.55–5.8 (m, 1H), 5.8–5.95 (m, 1H), 7.1–7.4 (m, 5H)5 a 1.4–1.75 (m, 2H), 1.85–2.25 (m, 3H), 2.25–2.5 (m, 1H), 2.85–3.45 (m, 5H), [[Truncated]]

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