Synthesis of spiro carbon linked deoxy disaccharides

Sharma, G. V. M.; Reddy, J. Janardhan; Rao, M. H. V. Ramana; Gallois, Nicolas

doi:10.1016/s0957-4166(02)00466-4

Cited by 6 publications

(2 citation statements)

References 15 publications

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“…[102] Both 1,4-and 1,5-diols can be converted into lactols by selective oxidation with IBX and subsequent cyclization of the hydroxy carbonyl compound thus formed (Scheme 11). [105,106] Further oxidation of lactols to lactones is Scheme 8. Selected examples of chemoselective alcohol oxidation.…”

Section: Simple Oxidation Of Alcohols and Diolsmentioning

confidence: 99%

“…Besides the selective oxidation of 1,4-and 1,5-diols to the respective lactols initally described by Corey and Palani, [105,106] there are numerous examples of the analogous formation of cyclic hemiaminals in the total synthesis of complex natural products. [109][110][111][112][113][114][115] For example, Eggleston and co-workers employed an oxidative ring closure of this type in the final step of the total synthesis of the potent chitinase inhibitor argadin (72,Scheme 25).…”

Section: Selected Applications In Total Synthesismentioning

confidence: 99%

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2‐Iodoxybenzoic Acid—A Simple Oxidant with a Dazzling Array of Potential Applications

2011

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Since its discovery by Christoph Hartmann and Victor Meyer in 1893, 2-iodoxybenzoic acid (IBX) has emerged as a rather ubiquitous oxidant for organic synthesis. The past decade has seen the development of a large variety of applications that go far beyond the simple oxidation of alcohols. This Review is concerned with the synthetic potential of IBX, with particular emphasis on uncommon reactivity patterns and novel fields of application.

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Section: Simple Oxidation Of Alcohols and Diolsmentioning

confidence: 99%

Section: Selected Applications In Total Synthesismentioning

confidence: 99%

2‐Iodoxybenzoic Acid—A Simple Oxidant with a Dazzling Array of Potential Applications

2011

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2‐Iodoxybenzoesäure – ein einfaches Oxidationsmittel mit einer Vielfalt an Anwendungsmöglichkeiten

Duschek

Kirsch

2011

Angewandte Chemie

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Seit seiner Entdeckung durch Christoph Hartmann und Victor Meyer im Jahr 1893 hat sich 2‐Iodoxybenzoesäure (IBX) zu einem geradezu ubiquitär einsetzbaren Oxidationsmittel entwickelt. Insbesondere in den vergangenen zehn Jahren wurde eine Vielzahl von Anwendungsmöglichkeiten beschrieben, die weit über die einfache Oxidation von Alkoholen hinausgehen. Dieser Aufsatz behandelt das Potenzial von IBX in der Synthese, wobei insbesondere unerwartete Reaktivitäten und moderne Anwendungen im Mittelpunkt der Diskussion stehen.

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The influence of electronic factors on palladium-mediated cycloisomerization: a systematic investigation of competitive 5-exo-dig versus 6-endo-dig cyclizations of sugar alkynols

et al. 2008

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Synthesis of spiro carbon linked deoxy disaccharides

Cited by 6 publications

References 15 publications

2‐Iodoxybenzoic Acid—A Simple Oxidant with a Dazzling Array of Potential Applications

2‐Iodoxybenzoic Acid—A Simple Oxidant with a Dazzling Array of Potential Applications

2‐Iodoxybenzoesäure – ein einfaches Oxidationsmittel mit einer Vielfalt an Anwendungsmöglichkeiten

The influence of electronic factors on palladium-mediated cycloisomerization: a systematic investigation of competitive 5-exo-dig versus 6-endo-dig cyclizations of sugar alkynols

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