Chapters authored
Anti-Corrosive Properties of Alkaloids on Metals
Numerous organic inhibitors have been reported to be used for the corrosion inhibition of various metals, especially, the heterogeneous ring compounds bearing larger electronegativity atoms (i.e., N, O, S, and P), polar functional groups, and conjugated double bonds are the most effective inhibitors. Based on the concept of green chemistry, in recent years, the research of corrosion inhibitor has gradually extracted new environment-friendly corrosion inhibitor from natural animals and plants, because of its advantages in wide source, low cost, low toxicity and subsequent treatment. Alkaloids such as papaverine, strychnine, quinine, nicotine, etc., have been studied as inhibitors for metals corrosion in corrosive media. This chapter aims to review the application of alkaloids for the corrosion inhibition of metals in corrosive media, and the development trend in this field is prospected.
Part of the book: Alkaloids
Approaches to the Total Synthesis of Puupehenone-Type Marine Natural Products
Puupehenones have been isolated from the marine sponge Chondrosia chucalla, which belong to a growing family of natural products with more than 100 members. These marine natural products have attracted increasing attention mainly due to their wide variety of biological activities such as antitumor, antiviral, and anti-HIV, and thus offer promising opportunities for new drug development. This chapter covers the approaches to the total synthesis of puupehenone-type marine natural products including puupehenol, puupehenone, puupehedione, and halopuupehenones. The routes begin with the construction of their basic skeletons, followed by the modification of their C- and D-rings. The contents are divided into two sections in terms of the key strategies employed to construct the basic skeleton. One is the convergent synthesis route with two synthons coupled by nucleophilic or electrophilic reaction, and the other is the linear synthesis route with polyene series cyclization as a key reaction.
Part of the book: Organic Synthesis