2000
DOI: 10.1070/rc2000v069n05abeh000561
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Sulfones and sulfoxides in the total synthesis of biologically active natural compounds

Abstract: A graphical treatment of the tone reproduction problem in television systems satisfactorily answered by extensive experimental work, using the techniques of subjective appraisal which have been increasingly developed in recent years. Direct comparison of a reproduction and an original, with all the parameters of the system accurately known, calls, of course, for a considerable experimental effort. Such limited observations as have been made, however, suggest that the shape of the curves at least gives a good i… Show more

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Cited by 185 publications
(109 citation statements)
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References 387 publications
(374 reference statements)
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“…The reaction was not completed within 24 h (Table 1, entry 6). Consequently, it was performed in different molar ratios of the catalyst in the presence of oxidant in order to obtain the optimum reaction conditions (Table 1, entries [1][2][3][4][5].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The reaction was not completed within 24 h (Table 1, entry 6). Consequently, it was performed in different molar ratios of the catalyst in the presence of oxidant in order to obtain the optimum reaction conditions (Table 1, entries [1][2][3][4][5].…”
Section: Resultsmentioning
confidence: 99%
“…Sulfoxides are important intermediates in the synthesis of various natural products [1,2]. Omeprazole and Figpronil pesticides are two typical examples of extensive applications of these important intermediates in pharmaceutical and fine chemical industries [3].…”
mentioning
confidence: 99%
“…中间体, 可用来制备醛、酮、炔烃、烯烃、烷烃、卤代 烷等化合物 [49] . 诸多有机金属试剂对 α,β-不饱和砜的不 对称加成可用来合成这类砜 [50,51] [60,61] (Scheme 2).…”
Section: β-位具有手性中心的砜是有机合成中的一种重要unclassified
“…Accordingly, alkanes bearing two geminal sulfonyl groups (gem-bisA C H T U N G T R E N N U N G (sulfonyl)s) may be regarded as synthetic equivalents of nucleophilic alkyl units with multiple applications in the field of natural product synthesis. [2] For years, realization of this concept has mainly relied on 1) irreversible generation of the sulfonyl a-carbanion by treatment with stoichiometric base in a separate step, 2) subsequent reaction with the corresponding electrophile; and 3) final reductive elimination of the sulfonyl group by action of metallic sodium or magnesium. [1][2][3] Although more advanced, direct methods capable of merging steps (1) and (2) by means of catalytic activation of the substrates still remain challenging.…”
Section: Introductionmentioning
confidence: 99%
“…[2] For years, realization of this concept has mainly relied on 1) irreversible generation of the sulfonyl a-carbanion by treatment with stoichiometric base in a separate step, 2) subsequent reaction with the corresponding electrophile; and 3) final reductive elimination of the sulfonyl group by action of metallic sodium or magnesium. [1][2][3] Although more advanced, direct methods capable of merging steps (1) and (2) by means of catalytic activation of the substrates still remain challenging. To date, sulfone-based direct catalytic C-C bond-forming methods are confined to either a-fluoro bis(phenylsulfonyl)methane [4] or monosulfones bearing an additional carbonyl, ester, or nitrile group at the a-position (Scheme 1).…”
Section: Introductionmentioning
confidence: 99%