Sophisticated commercial products and product assemblies can greatly benefit from novel IT-based approaches to the conditioning of these products and of „product knowledge‟, leading to what we call Smart Products. The paper motivates the need for such novel approaches, introduces important relevant challenges and research domains, and provides an early definition of Smart Products.

An enantioselective ring-expanding cycloisomerization of 1,5-enynes bearing a cyclopropylidene moiety has been developed. This methodology provides a new approach to bicyclo[4.2.0]octanes, a structural motif present in many biologically active natural products.

Utilizing a late-stage enamine bromofunctionalization strategy, the twelve-step total synthesis of (-)-huperzine Q was accomplished. Furthermore, the first total syntheses of (+)-lycopladines B and C are described. An unprecedented X-ray crystal structure of an unusual epoxyamine intermediate is also reported, and the synthetic application of this intermediate in natural product synthesis is de...

A variation of the Almost Ideal Demand System (AIDS) model of Deaton and Muellbauer (1980) has been employed to determine the impacts of per capita total expenditure, food prices and demographic variables on household demand for dairy products in Bangladesh. The budget shares are generally more responsive to per capita total expenditure than to prices. With respect to demographic effects, it is...

The synthesis of (-)-epibatidine has been accomplished utilizing a highly exo-selective asymmetric hetero Diels-Alder reaction. The key steps employed to transform the resulting bicycle into the natural product include a fluoride-promoted fragmentation and a Hofmann rearrangement. Reaction: see text.

In the last decades, marine natural products (MNPs), have attracted extensive interest from both chemists and pharmacologists due to their chemical and bioactive diversities. This special issue, collecting total synthesis and structural modification of six different type of bioactive MNPs, is expected to inspire and attract more research effects invested into MNP research.

A concise and scalable synthesis of a cis-fused bicyclo[5.3.0]decane ring system has been developed for the total synthesis of echinopines. The core of the natural products was constructed efficiently through an intramolecular 1,3-dipolar cycloaddition and ring contraction strategy.

This is a segment of the Literature Review chapter of a working paper titled, “Introducing Sugar Cane Juice in the Foreign MarketA Thorough Market Potential”. The paper entails a detailed analysis of the market segment strategy for the betterment of unders tanding and ensuring essentials in considering the right customer class to push the natural product to. The report is still in field level a...

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