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Volumn 73, Issue 9, 2008, Pages 3384-3391

Stereocontrolled photocyclization of 1,2-diketones: Application of a 1,3-acetyl group transfer methodology to carbohydrates

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATES; CONFORMATIONS; CYCLIZATION; FUNCTIONAL GROUPS; PHOTOCHEMICAL REACTIONS;

EID: 43449125629     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702663w     Document Type: Article
Times cited : (84)

References (65)
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    • Three different light sources were used: Sunlight: Direct sunlight: a bright sunny day, on cloudy days the reaction was considerably slower; UV lamp: 450 W ACE-Hanovia medium-pressure mercury lamp in an immersion well with 4.8 mm Pyrex walls; Daylight lamp: Philips lamp (master PL electronic, 23 W/865).
    • Three different light sources were used: Sunlight: Direct sunlight: a bright sunny day, on cloudy days the reaction was considerably slower; UV lamp: 450 W ACE-Hanovia medium-pressure mercury lamp in an immersion well with 4.8 mm Pyrex walls; Daylight lamp: Philips lamp (master PL electronic, 23 W/865).
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    • Complete details of the synthesis of all the 1,2-diketone precursors are provided in the Supporting Information.
    • Complete details of the synthesis of all the 1,2-diketone precursors are provided in the Supporting Information.
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    • 2S for this selective oxidation does not have precedents in the literature and resulted in an improved reagent for various models.
    • 2S for this selective oxidation does not have precedents in the literature and resulted in an improved reagent for various models.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.