SCOPUS 정보 검색 플랫폼

Volumn 29, Issue 12, 1988, Pages 1391-1394

Asymmetric synthesis XIV: A short and efficient synthesis of 3,5-disubstituted pyrrolizidine alkaloids via the CN(R,S) method

a CNRS (France)

Author keywords

[No Author keywords available]

Indexed keywords

PYRROLIDINE DERIVATIVE;

DRUG ANALYSIS; METHODOLOGY; NONHUMAN;

EID: 0023845520 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)80305-6 Document Type: Article

Times cited : (33)

References (13)

5
- 0000882942
- (1980) J. Org. Chem. , vol.45 , pp. 4778
- Jones¹ Blum² Fales³ Thompson⁴

6
- 37049093317
- Enantioselective synthesis of an ant venom alkaloid (?)-[3S-(3?, 5? 8?)]-3-heptyl-5-methylpyrrolizidine
- For the only enantioselective synthesis of 12 see
- (1983) Journal of the Chemical Society, Chemical Communications , pp. 1172
- Takano¹ Otaki² Ogasawara³

7
- 37049073213
- Stereoselective synthesis of pyrrolizidine alkaloids via substituted nitrones
- A stereoselective synthesis of (±) 11 has been recently published
- (1986) Journal of the Chemical Society, Chemical Communications , pp. 1017
- Lathbury¹ Gallagher²

8
- 84918482767
- 13C NMR) and high resolution mass data. We thank Dr. S.K. Kan (Institut d'Electronique Fondamentale, Université de Paris-Sud) for the use of his 400 MHz NMR spectrometer, .

9
- 84918482766
- 3), 50 MHz δ (ppm): 23.7, 30.2, 30.3, 35.6, 64.5, 66.7, 68.4, 73.0, 99.0, 110.1, 126.7, 127.9, 128.4, 143.3.

10
- 84918482765
- S. Arseniyadis, P.Q. Huang, D. Piveteau and H.-P. Husson, Tetrahedron accepted for publication.

11
- 84918482764
- 3, 50 MHz) δ (ppm): 14.0, 22.5, 23.7, 26.9, 27.7, 28.8, 29.1, 29.6, 31.7, 32.9, 36.2, 36.5, 60.8, 60.9, 62.3, 63.3, 64.5, 109.7, 127.4, 128.1, 129.1, 139.8.

12
- 84918482763
- 3, 50 MHz) δ (ppm): 14.2, 22.7, 24.0, 26.8, 29.4, 29.8, 30.0, 31.9, 36.2, 58.2, 62.0, 64.2, 64.7, 65.2, 110.0, 127.9, 128.4, 129.1, 137.4.

13
- 84918482762
- The spectral data of synthetic (+) 11 were identical to those previously reported for the racemic material 7.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.