SCOPUS 정보 검색 플랫폼

Volumn 20, Issue 31, 1979, Pages 2857-2860

Nucleophilic displacement of activated aryl triflates a new synthesis of oxindoles and arylacetic acids

Author keywords

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Indexed keywords

EID: 0002426577 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(01)86434-0 Document Type: Article

Times cited : (21)

References (15)

1
- 0001401197
- (1955) J. Am. Chem. Soc. , vol.77 , pp. 700
- Stein¹ Bronner² Pfister³

3
- 37049053195
- 40. The influence of the nitro-group upon side-chain reactivity. Part II. The inhibition of the influence of the nitro-group upon ?-proton-extraction from 4-nitrobenzyl chloride
- (1961) Journal of the Chemical Society (Resumed) , pp. 221
- Hanna¹ Iskander² Salama³

5
- 33947481591
- 3 group on nucleophilic attack at the sulfur atom. Cf., Further discussion of the mechanistic aspects of the triflate displacement is deferred for a full publication.
- (1964) J. Am. Chem. Soc. , vol.86 , pp. 4645
- Bordwell¹ Brannen²

6
- 84917997870
- All new compounds had satisfactory analytical results and spectral data.

7
- 84917997869
- 3 in acetonitrile at reflux, the reaction requires 24 hr. Yields by the two methods appear to be comparable.

8
- 84917997868
- This experiment was carried out by Drs. J. Rokach and R. Lapalme.

10
- 0001603007
- Recent syntheses of oxindoles:
- (1974) J. Am. Chem. Soc. , vol.96 , pp. 5508
- Gassman¹ van Bergen²

14
- 0342876652
- For attempts to generate aryl cations from aryl triflates see:
- (1976) Tetrahedron Letters , pp. 1435
- Streitwieser¹ Dafforn²

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