SCOPUS 정보 검색 플랫폼

Volumn 220, Issue 4600, 1983, Pages 949-951

Total synthesis of the L-hexoses

Author keywords

[No Author keywords available]

Indexed keywords

HEXOSE;

METHODOLOGY; NONHUMAN;

EID: 0020645466 PISSN: 00368075 EISSN: None Source Type: Journal
DOI: 10.1126/science.220.4600.949 Document Type: Article

Times cited : (186)

References (10)

1
- 84889288508
- This report is part 5 in a series on the synthesis of saccharides and polyhydroxylated natural products. For part 4, see in press
- J. Am. Chem. Soc.
- Reed, L.A.¹ Ito, Y.² Masamune, S.³ Sharpless, Κ.B.⁴

10
- 84913735041
- Attempts to deprotect the L-altrose derivative with trifluoroacetic acid, followed by catalytic hydrogenation, invariably gave 1,6-anhydro-β - L-altropyranose, which is known to exist in acid solutions in equilibrium with the free sugar W. W. Pigman and M. L. Wolfram, Eds. Academic Press, New York Exposure of commercially obtained d-altrose to acid also produced the 1,6-anhydro-β -D-altropyranose, which upon acetylation proved identical to the synthetic peracetylated β-L-l,6-anhydro derivative
- (1946) Advances in Carbohydrate Chemistry , vol.2 , pp. 38
- Peat, S.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.