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Volumn 17, Issue 9, 2011, Pages 2633-2641

Total synthesis of cyclo-mumbaistatin analogues through anionic homo-fries rearrangement

Author keywords

natural products; phosphatase inhibitor; polyketides; spirolactones; total synthesis

Indexed keywords

NATURAL PRODUCTS; PHOSPHATASE INHIBITOR; POLYKETIDES; SPIROLACTONES; TOTAL SYNTHESIS;

EID: 79951775575     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201003166     Document Type: Article
Times cited : (38)

References (122)
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    • The anionic homo-Fries rearrangement has been successfully applied as a particular powerful method for the preparation of tetra-ortho-substituted benzophenones, such as the prominent PKC inhibitor balanol
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    • For preparative purposes the photolysis of 1-alkylanthraquinones has found miscellaneous application in their benzylic oxidation. For examples see
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    • note
    • The TIPS-protecting group has been proved to be the most base-resistant silyl protecting group. Therefore, we anticipated a triisopropylsilylalkyl ether to stay untouched under the strong basic conditions (pH ⥠12) of the planned reductive methylation of rac-44.
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    • 8]toluene, supported by the calculation of selected spin systems with DNMR.
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    • CCDC799897 (11), 799901 (rac-22), 799898 (30), 799899 (31), and 799900 (35) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.