SCOPUS 정보 검색 플랫폼

Volumn 35, Issue 40, 1994, Pages 7451-7454

Dispiroketals in synthesis (Part 13): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective diels-alder reactions using a bifunctional, C2- symmetrical chiral auxiliary

(4) Bezuidenhoudt, Barend C B a Castle, Grant H a Geden, Joanna V a Ley, Steven V a

a UNIVERSITY OF CAMBRIDGE (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL; SPIRO COMPOUND;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY;

BETULACEAE;

EID: 0028129923 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/0040-4039(94)85339-8 Document Type: Article

Times cited : (16)

References (5)

1
- 84912953795
- C, 50 [[Truncated]]

2
- 33845280186
- Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinones
- (1988) Journal of the American Chemical Society , vol.110 , pp. 1238
- Evans¹ Chapman² Bisaha³

3
- 84912968191
- 2 (1 M in DCM, 1 mmol). The deep red solution was stirred for 15 minutes and treated with the diene (50 mmol). The reaction was allowed to come to room temperature and stirred for between 1–16 hours. After diluting with DCM (50 ml), 1N HCl (10 ml) was added and the aqueous phase extracted with DCM (2 × 50 ml). The combined organic layers were washed with brine (2 × 30 ml), dried (MgSO4), concentrated in vacuo and the products obtained by flash column chromatography.

4
- 0000188220
- .alpha.,.beta.-Unsaturated oxazolines, a powerful tool in asymmetric Diels-Alder cycloadditions
- Literature data for hydrolysis products of (3), (6a) and (6b)
- (1990) Journal of the American Chemical Society , vol.112 , pp. 6672
- Kouklovsky¹ Pouilhès² Langlois³

5
- 0039788741
- Syntheses and chiroptical properties of (+)-2-brendanone and its analogs
- (6c) and (6d), See also reference 3
- (1979) The Journal of Organic Chemistry , vol.44 , pp. 16
- Nakazaki¹ Naemura² Kondo³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.