Dissertation Writing Chapter 1 - YouTube

I have messed up on one of the chapters in my final year dissertation and now I have to write 3 chapters 6,000 words in one week, plus complete 2 assignments for other subjects. I have no idea what I should type about that will not only be interesting but also could make it long enough to type a 20 page paper about. But I need to set myself some sort of limit as it's a broad topic. Where can I get information on how to structure the paper, how many chapters, what goes into the dissertation chapter 1? Just give me ideas and I will see if it’s in one of these chapters.

How to write dissertation chapter 1? - Current Affairs

The dissertation chapter 1 is one that requires extra consideration. It's important to keep in mind that the first impression the reader gets, is from this section. It is truly key in outlining the concept of your dissertation as this is where that first impression you want to convey continues to the end. Be careful that you include enough information to motivate readers but not too many details so that the reader wouldn’t get bored and bothered. This is where the information regarding subject matter is found being the very first thing that is read.

How to write dissertation chapter 1

Dissertation Chapter 1 Length - .xyz

This dissertation comprises the design, synthesis, and biological evaluation of nine new jasplakinolide analogs and studies toward a total synthesis of neopeltolide. ^ Dissertation Chapter 1 explains the rationale for analog design, synthetic strategy, and biological results for new jasplakinolide derivatives. Jasplakinolide is an F-actin-inducer and potent cytotoxic agent, which has the potential to treat cancer. The general synthesis path which allowed access to these analogs was based on a previous route designed by our group for the synthesis of jasplakinolide. Key reactions include a Yamaguchi macrolactonization step, an Evans' syn-aldol reaction, and an efficient o-ester Claisen rearrangement. Structural changes to the non-peptide portion of jasplakinolide produced analogs which maintained potent anticancer activity. One compound, which has shown similar activity to jasplakinolide, was accessed via a simplified synthetic scheme and was less structurally complex than the parent molecule. This simplified analog presents an advantageous platform for further derivative studies. Chapter 2 of this dissertation details research toward a total synthesis of the marine natural product (+)-neopeltolide. Neopeltolide has shown impressive biological activity, including selectivity for certain cancer cell lines. Our synthetic strategy allowed for the construction of the macrocyclic core by utilizing a hetero Diels-Alder reaction catalyzed by Jacobsen's chromium tridentate complex. Additional key reactions include a Horner-Wadsworth-Emmons reaction, a Yamaguchi macrolactonization, and two Brown asymmetric allylations. Also described in this chapter is the recent progress toward a novel synthesis of the oxazole side chain of neopeltolide. The key reactions for the synthesis of the oxazole side chain are a copper-zinc coupling and a Wipf-type cyclodehydration reaction to form the oxazole ring. This approach to the oxazole side chain and the macrolactone should allow for access to novel derivatives.^