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Tetrahedron Letters

Volumn 34, Issue 35, 1993, Pages 5519-5522

A concise synthesis of the novel antibiotic aranorosin

(5) McKillop, Alexander a McLaren, Lee a Watson, Robert J a Taylor, Richard J K a Lewis, Norman b

a UNIVERSITY OF EAST ANGLIA (United Kingdom)

b GLAXOSMITHKLINE (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; ARANOROSIN;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0027225683 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)73870-6 Document Type: Article

Times cited : (37)

References (18)

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2
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- (1988) J. Antibiot. , vol.41 , pp. 1780-1784
- Roy¹ Mukhopadhyay² Reddy³ Desikan⁴ Rupp⁵ Ganguli⁶

3
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- (1988) J. Antibiot. , vol.41 , pp. 1785-1794
- Fehlhaber¹ Kogler² Mukhopadhyay³ Vijayakumar⁴ Roy⁵ Rupp⁶ Ganguli⁷

4
- 0002287868
- Synthetic Studies Towards Aranorosin
- (1992) Synlett , pp. 201-203
- McKillop¹ McLaren² Taylor³ Watson⁴ Lewis⁵

5
- 0026497864
- Organometallic additions to protected quinone bis-epoxides and quinone monoacetals: synthesis of the aranorosin nucleus
- (1992) Journal of the Chemical Society, Chemical Communications , pp. 1589-1591
- McKillop¹ Taylor² Watson³ Lewis⁴

6
- 1842613077
- An Improved Synthesis of the Aranorosin Nucleus
- (1992) Synlett , pp. 1005-1006
- McKillop¹ Taylor² Watson³ Lewis⁴

7
- 0026076709
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- Rama¹ Gurjar² Sharma³

8
- 0027252816
- (1993) J. Org. Chem. , vol.58 , pp. 1649-1650
- Wipf¹ Kim²

9
- 0000179169
- (1991) J. Org. Chem. , vol.56 , pp. 435-438
- Kita¹ Tohma² Kikuchi³ Inagaki⁴ Yakura⁵

10
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- Tamura¹ Yakura² Haruta³ Kita⁴

11
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- (1988) Tetrahedron Lett. , vol.29 , pp. 677-680
- Pelter¹ Elgendy²

12
- 84918712492
- Prepared by DibalH reduction of the corresponding esters [see (9) 〉 (10), Scheme 2].

13
- 84918755760
- All new compounds gave consistent spectral and analytical/mass spectrometric data.

14
- 84918712887
- 2-Pd/C) and acylated (PhCOCl), but the yields were low.

15
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- and references therein
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- Evans¹ Gage²

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17
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- 2)]. The alcohols (6a) and (6b) were shown to be enantiomerically pure by NMR spectroscopy on their Mosher ester derivatives.

18
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- 2-NaOH in methanol gave ca. 17% of the required bis-epoxide (1a).

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.