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Volumn 75, Issue 8, 2010, Pages 2681-2701

Ladder polyether synthesis via epoxide-opening cascades directed by a disappearing trimethylsilyl group

Author keywords

[No Author keywords available]

Indexed keywords

BASIC CONDITIONS; GENERAL METHOD; NATURAL PRODUCTS; TRIMETHYLSILYL; TRIMETHYLSILYL GROUPS;

EID: 77950969628     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1002455     Document Type: Article
Times cited : (20)

References (102)
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    • Our laboratory has also reported another approach to this problem, one in which no directing groups are attached to the epoxides and in which the cascades were conducted in aqueous environments: Vilotijevic, I.; Jamison, T. F. Science 2007, 317, 1189-1192 This work and other recent related investigations are described at the end of the Results and Discussion section of this manuscript
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    • 2, (2-thiophene)Cu(CN)Li) proved either unreactive or served to scramble the E / Z geometry of the alkenyl product.
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    • See Supporting Information for details for details of the preparation of 36
    • See Supporting Information for details for details of the preparation of 36.
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    • This compound was produced in analogous fashion as polyepoxides 35, 24, 28. For details see Supporting Information
    • This compound was produced in analogous fashion as polyepoxides 35, 24, 28. For details see Supporting Information.
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    • See Supporting Information for the details of the preparation of 43.
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    • tBu/DMF, CsF, CsOH in THF, DMF, and MeOH) gave no desired product, with decomposition and elimination predominating.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.