SCOPUS 정보 검색 플랫폼

Volumn 1990, Issue 1, 1990, Pages 15-21

Synthesis of a protected C‐11/C‐17 segment of mycinolide‐V

Author keywords

Alkoxyalkylation; Enolate alkylation; Mycinolide V

Indexed keywords

EID: 84986642230 PISSN: 01702041 EISSN: 10990690 Source Type: Journal
DOI: 10.1002/jlac.199019900103 Document Type: Article

Times cited : (10)

References (15)

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- Stereoselektive Synthese von Alkoholen, XII. Synthese der C-9/C-13-Teilstruktur des Methynolids
- (1983) Chemische Berichte , vol.116 , pp. 1631
- Hoffmann, R.W.¹ Ladner, W.²

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- Stereoselektive Synthese von Alkoholen, XV. Stereoselektive Synthese von α-Alkyl-α,β-dihydroxy-carbonsäureester-Derivaten: Synthese der ( + )-Viridiflorsäure
- (1983) Chemische Berichte , vol.116 , pp. 3413
- Ladner, W.¹

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- Totalsynthese von Mycinolid V, dem Aglycon eines Makrolid-Antibioticums der Mycinamycin-Reihe
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- Ditrich, K.¹ Bube, T.² Stürmer, R.³ Hoffmann, R.W.⁴

13
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- 0. 6. However, this highly selective transformation could not be incorporated into our mycinolide synthesis, since later cleavage of pinacolone‐derived dioxolanes requires even more harsh conditions than that of acetonides.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.