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Volumn 47, Issue 36, 2008, Pages 6877-6880

Dynamic stereochemistry transfer in a transannular aldol reaction: Total synthesis of hypocrellin A

Author keywords

Biaryls; Cyclization; Dynamic stereochemical transfer; Natural products; Total synthesis

Indexed keywords

BIOMIMETICS; CHEMICAL REACTIONS; STEREOCHEMISTRY;

EID: 52449083568     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200800734     Document Type: Article
Times cited : (56)

References (62)
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    • hypocrellin A is called shiraiachrome B here, see Ref, 9
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    • Here , we employ the names and structural assignments suggested by: S. Mazzini, L. Merlini, R. Mondelli, L. Scagloni, J. Chem. Soc. Perkin Trans. 2 2001, 409-416. Note: SciFinder indexes hypocrellin and hypocrellin A as identical compounds with the absolute configuration of hypocrellin.
    • Here , we employ the names and structural assignments suggested by: S. Mazzini, L. Merlini, R. Mondelli, L. Scagloni, J. Chem. Soc. Perkin Trans. 2 2001, 409-416. Note: SciFinder indexes hypocrellin and hypocrellin A as identical compounds with the absolute configuration of hypocrellin.
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    • For related examples involving axial to central chirality transfer, see: a
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    • There is one report of an acyclic intramolecular aldol to yield the seven-membered ring through a reductive aldol reaction of the enone aldehyde: T. G. Baik, A. L. Luis, L. C. Wang, M. J. Krische, J. Am. Chem. Soc. 2001, 123, 5112-5113
    • There is one report of an acyclic intramolecular aldol to yield the seven-membered ring through a reductive aldol reaction of the enone aldehyde: T. G. Baik, A. L. Luis, L. C. Wang, M. J. Krische, J. Am. Chem. Soc. 2001, 123, 5112-5113.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.