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Volumn 59, Issue 30, 2003, Pages 5623-5634

Biosynthetic inspirations: Cationic approaches to cyclopropane formation

Author keywords

Cation; Cyclopropyl; Homoallyl

Indexed keywords

CATION; CHOLESTEROL ESTER TRANSFER PROTEIN; CONSTALACTONE A; CONSTALACTONE B; CYCLOPROPANE DERIVATIVE; FR 900848; HALICHOLACTONE; LACTONE DERIVATIVE; PROTEIN INHIBITOR; SOLANDELACTONE A; SOLANDELACTONE B; U 106305; UNCLASSIFIED DRUG;

EID: 0038306262     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00880-9     Document Type: Review
Times cited : (65)

References (66)
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    • Sato had previously shown that β -stannyl carbonyl compounds react with Lewis acids to provide cyclopropanols
    • (b). Sato had previously shown that β -stannyl carbonyl compounds react with Lewis acids to provide cyclopropanols Sato T., Watanabe, Murayama E. Tetrahedron Lett. 27:1986;1621.
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  • 42
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    • For a seminal discussion of these intermediates, see: (a). and (b). For an early suggested biosynthesis for cyclopropane fatty acids based on the homoallyl cation see (c)
    • For a seminal discussion of these intermediates, see: (a) Roberts J.D., Mazur R.H. J. Am. Chem. Soc. 73:1951;2509. and (b) Olah G.A., Reddy P., Prakash G.K.S. Chem. Rev. 92:1992;69-95. For an early suggested biosynthesis for cyclopropane fatty acids based on the homoallyl cation see (c) Kosower E.M. Science. 113:1951;605.
    • (1951) Science , vol.113 , pp. 605
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.