第一部份 中文摘要
在室溫下，利用碘(iodine)催化indole和pyrrol對nitroolefins進行Michael加成進而得到indolyl nitroalkane 5 和 pyrrolyl nitroalkane 7。相較於已知的路易士酸或貴重金屬當催化劑來說，此方法具有反應時間短及高產率的優點。

第二部份 中文摘要
在無溶劑的條件之下，利用碘 (iodine) 及2,4,6-trichloro﹝1,3,5﹞triazine (TCT) 加速醛 (aldehyde) 或酮 (ketone)、苯胺(aniline) 和亞磷酸三乙酯 (triethylphosphite)合成-胺基磷酸鹽類(-amino phosphonate)，此反應可在室溫或是60 oC條件下，以一鍋的方式進行反應得到高產率的產物。

第三部份 中文摘要
在室溫下，利用碘(iodine)催化醛、苯胺和acetylcyclohenxene以具有選擇性的特性，一鍋合成trans-endo-decahydroquinolin-4-one；此方法具有易操作、反應時間短、高產率、單一產物已及溫和的反應條件的優點。

第四部份 中文摘要
利用碘(iodine)催化醛和2-hydroxyacetophenone一鍋合成flavanone，此方法具有易操作、高產率、單一產物以及適用於各種官能基的優點。

第五部份 中文摘要
3-Amino chromans的衍生物在神經生物學及藥物學上，扮演極重要的腳色，因此發展有效率的合成方法為當務之急。我們利用salicylaldehyde 1 和nitromethane 經由 Knovenagel 反應路徑，接著走Michael 加成及aldol 的反應機構，在一鍋的條件下，合成出3-amino chromans的衍生物。

part 1 Reference

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