SCOPUS 정보 검색 플랫폼

Volumn 29, Issue 22, 1988, Pages 2711-2714

Oxidative ring contraction of benzeneselenenate adducts of glycal ethers. synthesis of showdomycin analogues

Author keywords

[No Author keywords available]

Indexed keywords

SHOWDOMYCIN DERIVATIVE; UNCLASSIFIED DRUG;

DRUG SYNTHESIS; NONHUMAN;

EID: 0023920629 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/0040-4039(88)85267-5 Document Type: Article

Times cited : (40)

References (12)

1
- 85069096476
- A. Kaye, S. Neidle, and C.B. Reese, Tetrahedron Lett., in the press.

4
- 37049111829
- Glycosyloxyselenation?deselenation of glycals: a new approach to 2?-deoxy-disaccharides
- (1981) Journal of the Chemical Society, Chemical Communications , pp. 572
- Jaurand¹ Beau² Sinaÿ³

6
- 85069098398
- 3: δ24.26, 27.37, 44.17, 55.60, 62.78, 103.17, 127.73, 129.06, 129.13, 134.92], it is clear that (8a) is diastereoisomerically pure.

7
- 84971061986
- Studies on unsaturated sugars with particular reference to the synthesis of 6-Deoxy-6-fluoro derivatives
- (1976) Australian Journal of Chemistry , vol.29 , pp. 381
- Blackburne¹ Fredericks² Guthrie³

8
- 85069099535
- 2O, may be assigned to H-l. The signal at δ3.28 (1H, dd, J 3.2, 11.0 Hz), which collapses to a sharp doublet (J 11.0 Hz) on irradiation at δ5.35, may be assigned to H-2. From the size of the coupling constants, it appears that H-1 is equatorially disposed and that H-2 and H-3 are both axially disposed.

9
- 85069108328
- 2SO] into 3,4,6-tri-O-benzyl-d-galactal (14), m.p. 57–58°C, in 51% overall yield.

10
- 0004111991
- R.L. Whistler, M.L. Wolfrom, Academic, New York and London
- (1963) Methods in Carbohydrate Chemistry , vol.2 , pp. 405-408
- Roth¹ Pigman²

12
- 85069104730
- 2O]. The resonance signals at δ5.34 (1H, d, J 4 Hz) and 3.60 (1H, dd, J 4, 11 Hz) have tentatively been assigned to H-1 and H-2, respectively.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.