SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Tetrahedron Letters

Volumn 19, Issue 4, 1978, Pages 315-318

Vinylogous amide anions. Application to the synthesis of 2,3-dihydro-4-pyrones

(2) Vinick, Fredric J a Gschwend, Heinz W a

a NOVARTIS PHARMA AG (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 49349135918 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(01)85113-3 Document Type: Article

Times cited : (13)

References (19)

1
- 0009610565
- (1974) Tetrahedron Lett. , pp. 3963
- Bryson¹ Gammill²

2
- 85012429065
- Alkylations of Vinylogous Amides, Vinylogous Esters and Vinylogous Thioesters with Potassium Hydride
- (1976) Synthesis , pp. 401
- Gammill¹ Bryson²

3
- 0343248950
- (1973) Tetrahedron Lett. , pp. 39
- Yoshimoto¹ Ishida² Hiraoka³

4
- 0017263499
- (1976) J. Am. Chem. Soc. , vol.98 , pp. 224
- Ganem¹

5
- 0342931115
- The following references represent a selection of recent syntheses of 2,3-dihydro-4-pyrones
- (1973) Tetrahedron Lett. , pp. 577
- Sher¹ Isidor² Taneja³ Carlson⁴

6
- 0042868628
- (1966) Tetrahedron Lett. , pp. 233
- Casnati¹ Quilico² Ricca³ Finza⁴

7
- 84980302113
- Nouvelle voie d'accès aux 1H-dihydro-2,3 pyridones-4
- (1976) Journal of Heterocyclic Chemistry , vol.13 , pp. 253
- Eskenazi¹ Lhommet² Richaud³ Maitte⁴

8
- 84914338235
- (1968) J. Pharm. Soc. Jap. , vol.88 , pp. 1044
- Nakanishi¹ Nagao² Okada³

9
- 0002501053
- (1968) Bull. Soc. Chim. Fr. , pp. 288
- Gelin¹ Gelin²

10
- 84918262000
- (1969) Bull. Soc. Chim. Fr. , pp. 1383
- Gelin¹ Gelin²

11
- 84914389267
- (1975) Bull. Soc. Chim. Fr. , pp. 305
- Gelin¹ Henry²

12
- 84914389266
- (1972) Bull. Soc. Chim. Fr. , pp. 2069
- Garry¹ Vessiere²

13
- 84914389265
- (1974) Bull. Soc. Chim. Fr. , pp. 933
- Garry¹ Nyffenegger² Vessiere³

14
- 84913077481
- (1968) Bull. Soc. Chim. Fr. , pp. 2926
- Bertrand¹ Rouvier²

15
- 8744294408
- (1965) J. Am. Chem. Soc. , vol.87 , pp. 3186
- Harris¹ Boatman² Hauser³

16
- 84914389264
- 2 followed by treatment of the product with dimethylamine/methanol at reflux.

17
- 84914389263
- 2 = H) was converted to its lithium salt and reacted with benzophenone, a crystalline condensation product of type 4 was obtained in 66% yield. However, this adduct was unchanged upon treatment with dilute HCl/methanol. Exposure to concentrated HCl afforded the dehydration product shown below.

18
- 84987311678
- Novel two step synthesis of pyrazoles and isoxazoles from aryl methyl ketones
- (1977) Journal of Heterocyclic Chemistry , vol.14 , pp. 345
- Lin¹ Lang²

19
- 84914389262
- When 3a was heated at reflux for 2 hr in 1:1 methanol/3N NaOH and the solution then acidified, phenylacetone was obtained in 89% yield.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.