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Tetrahedron Letters

Volumn 36, Issue 7, 1995, Pages 1039-1042

Ortho-metalated aromatic tertiary amides: New synthetic applications

(3) Casas, Ramon a Cavé, Christian a d'Angelo, Jean a

a CNRS (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; AROMATIC COMPOUND;

ARTICLE; CATALYSIS; COMPLEX FORMATION; DRUG SYNTHESIS; REACTION ANALYSIS;

EID: 0028873350 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/0040-4039(94)02436-F Document Type: Article

Times cited : (19)

References (20)

1
- 0002914069
- Reviews
- (1988) Bull. Soc. Chim. Fr. , pp. 67-78
- Snieckus¹

2
- 0012397313
- (1990) Chem. Rev. , vol.90 , pp. 879-933
- Snieckus¹

3
- 33845553899
- (1982) J. Org. Chem. , vol.47 , pp. 34-46
- Beak¹ Brown²

4
- 84915393233
- +).

5
- 84915393232
- +).

6
- 84915393231
- +).

7
- 84915393230
- 3) δ 7.12 (m, 10H), 2.85 (s, 4H).

8
- 0026625831
- (1992) Tetrahedron , vol.48 , pp. 4863-4878
- de Silva¹ Reed² Billedeau³ Wang⁴ Norris⁵ Snieckus⁶

9
- 0021238272
- 2:, (in that case, the condensation with allyl bromide led to the allylated derivatives with good yields)
- (1984) J. Org. Chem. , vol.49 , pp. 737-742
- Sibi¹ Miah² Snieckus³

10
- 0000897931
- 2
- (1986) J. Org. Chem. , vol.51 , pp. 271-273
- Sibi¹ Dankwardt² Snieckus³

11
- 0001497441
- Transmetalation of o-lithio aryloxazolines with CuBr:
- (1979) J. Org. Chem. , vol.44 , pp. 1533-1536
- Ellefson¹

12
- 0001606689
- 2O solution (30 min). The electrophiles were then added at this temperature
- (1984) Tetrahedron , vol.40 , pp. 5005-5038
- Lipshutz¹ Wilhelm² Kozlowski³

13
- 84915393229
- 3) δ 7.24 (dd, J = 8.2, 7.8 Hz, 1H), 6.84 (d, J = 7.8 Hz, 1H), 6.75 (d, J = 8.2 Hz, 1H), 5.94 (m, 1H), 5.04 (m, 2H), 3.79 (s, 3H), 3.79 (dq, J = 7.2, 14.1 Hz, 1H), 3.25 (m, 3H), 3.09 (dq, J = 7.2, 2.1 Hz, 2H), 1.25 (t, J = 7.2 Hz, 3H), 1.01 (t, J = 7.2 Hz, 3H).

14
- 84915393228
- 3) δ 7.21 (m, 4H), 5.89 (m, 1H), 5.04 (m, 2H), 3,68 (m, 1H), 3.34 (d, J = 6.7 Hz, 2H), 3.32 (m, 1H), 2.94 (q, J = 7.2 Hz, 2H), 1.21 (t, J = 7.2 Hz, 3H), 0.99 (t, J = 7.2 Hz, 3H).

15
- 84915393227
- 3) δ 7.15 (m, 9H), 3,94 (m, 2H), 3.54 (m, 1H), 3.22 (m, 1H), 2.73 (m, 2H), 1.12 (t, J = 7.2 Hz, 3H), 0.88 (t, J = 7.2 Hz, 3H).

16
- 84915393226
- +).

17
- 84915393225
- 3) δ 7.39 (m, 6H), 6.92 (m, 2H), 3.65 (s, 3H), 3.45 (q, J = 7.2 Hz, 2H), 3.14 (q, J = 7.2 Hz, 2H), 1.16 (t, J = 7.2 Hz, 3H), 1.01 (t, J = 7.2 Hz, 3H).

18
- 84915393224
- +).

19
- 84915393223
- +).

20
- 84915393222
- 3) δ 7.24 (m, 4H), 3.69 (m, 1H), 3.26 (m, 1H), 3.02 (q, J = 7.2 Hz, 2H), 2.91 (m, 1H), 2.73-2.00 (m, 6H), 1.75 (m, 2H), 1.14 (t, J = 7.2 Hz, 3H), 0.98 (t, J = 7.2 Hz, 3H).

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.