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Volumn , Issue 10, 2009, Pages 1477-1489

Stereocontrolled preparation of fully substituted cyclopentanes: Relevance to total synthesis

Author keywords

Asymmetric synthesis; Carbocycles; Cyclopentane; Diels Alder reaction; Natural products; Palau'amine; Total synthesis

Indexed keywords


EID: 64149121169     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200801229     Document Type: Article
Times cited : (95)

References (53)
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    • In the interest of brevity, those synthetic approaches to the aminocyclopentitol substructure of 6 that rely on fragmentation and refunctionalization of carbohydrate starting materials will not be addressed here. For representative examples, see
    • In the interest of brevity, those synthetic approaches to the aminocyclopentitol substructure of 6 that rely on fragmentation and refunctionalization of carbohydrate starting materials will not be addressed here. For representative examples, see:
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    • For a review of the chemistry and biology of aniinocyclopentitol glycosidase inhibitors covering literature through, see
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    • This Microreview focuses only on three natural product classes and is not intended to be a comprehensive treatment of the topic. For example, the cyclopentanes viridenomycin and hirsutellone B have also been compelling objectives for chemical synthesis; preparation of the tricyclic core of the hirsutellones has very recently been described wherein the central penta-substituted cyclopentane ring is formed in the course of a tandem acyl ketene-trapping/intramolecular Diels-Alder reaction: S. Tilley, K. Reber, E. J. Sorensen, Org. Lett, 2009, 11, 701-703
    • This Microreview focuses only on three natural product classes and is not intended to be a comprehensive treatment of the topic. For example, the cyclopentanes viridenomycin and hirsutellone B have also been compelling objectives for chemical synthesis; preparation of the tricyclic core of the hirsutellones has very recently been described wherein the central penta-substituted cyclopentane ring is formed in the course of a tandem acyl ketene-trapping/intramolecular Diels-Alder reaction: S. Tilley, K. Reber, E. J. Sorensen, Org. Lett, 2009, 11, 701-703.
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    • Total syntheses of (±)-axinellamines A and B
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    • D. O'Malley, J. Yamaguchi, I. Young, I. Seiple, P. S. Baran, Angew. Chem. Int. Ed. 2008, 47, 3581-3583; total syntheses of (±)-massadine and massadine chloride (5):
    • b) D. O'Malley, J. Yamaguchi, I. Young, I. Seiple, P. S. Baran, Angew. Chem. Int. Ed. 2008, 47, 3581-3583; total syntheses of (±)-massadine and massadine chloride (5):
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.