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Synthesis, Spectroscopic, and in Vitro Photosensitizing Efficacy of Ketobacteriochlorins Derived from Ring-B and Ring-D Reduced Chlorins via Pinacol–Pinacolone Rearrangement

机译：通过皮卡酚 - 针醇重排衍生自环-B和RONG-D减少氯的酮氯氯硫磷的合成，光谱和体外光敏效果

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Penny Joshi; Manivannan Ethirajan; Lalit N. Goswami; Avinash Srivatsan; Joseph R. Missert; Ravindra K. Pandey;
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年度 2011
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1. Synthesis, spectroscopic, and in vitro photosensitizing efficacy of ketobacteriochlorins derived from ring-B and ring-D reduced chlorins via pinacol-pinacolone rearrangement [J] . Joshi P., Ethirajan M., Goswami L.N., The Journal of Organic Chemistry . 2011,第21期

机译：经由频哪醇-频哪酮重排衍生自环B和环D还原二氢卟酚的酮氯霉素的合成，光谱和体外光敏功效
2. Scandium(III)‐Triflate‐Catalyzed Pinacol‐Pinacolone Rearrangement and Cyclization of 1,2‐Diaryl‐1,2‐Ethanediol: A Versatile Synthesis of 1‐Aryl‐2,3‐Dihydro‐1H‐3‐Benzazepines [J] . Ieawsuwan Winai, Pingaew Ratchanok, Kunkaewom Sukanya, Asian Journal of Organic Chemistry . 2019,第8期

机译：钪（III） - 催化催化的Pinacol-pinacolone重排和1,2-二芳基-1,2-乙二醇的环化：1-芳基-2,3-二氢-1H-Benzazines的通用合成
3. Highly Selective Synthesis Of The Ring-b Reduced Chlorins Byrnferric Chloride-mediated Oxidation Of Bacteriochlorins:rneffects Of The Fused Imide Vs Isocyclic Ring On Photophysicalrnand Electrochemical Properties [J] . Chao Liu, Mahabeer P, Dobhal, Journal of the American Chemical Society . 2008,第43期

机译：氯化亚铁介导的细菌氯霉素的氧化选择性选择性合成环b还原的氯霉素：融合酰亚胺对等环对光物理性质和电化学性质的影响
4. Synthesis Spectroscopic and In-vitro Photosensitizing Efficacy of Ketobacteriochlorins Derived from Ring-B and Ring-D Reduced Chlorins via Pinacol-Pinacolone Rearrangement [O] . Penny Joshi, Manivannan Ethirajan, Lalit N. Goswami, -1

机译：合成光谱及Ketobacteriochlorins从环B和环d衍生的体外功效光敏化通过频哪醇 - 频哪酮重排减少二氢卟酚
5. Comparative in Vitro and in Vivo Studies on Long-Wavelength Photosensitizers Derived from Bacteriopurpurinimide and Bacteriochlorin p6: Fused Imide Ring Enhances the in Vivo PDT Efficacy [O] . -1

机译：对比较的体外和体内研究，源自菌嘌呤酰亚胺和菌硫脲的长波长光敏剂，P6：熔融酰亚胺环增强了体内PDT功效

Synthesis, Spectroscopic, and in Vitro Photosensitizing Efficacy of Ketobacteriochlorins Derived from Ring-B and Ring-D Reduced Chlorins via Pinacol–Pinacolone Rearrangement

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