Results 291 to 300 of about 12,937,378 (338)

Total Synthesis of Neooxazolomycin [PDF]

Angewandte Chemie, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Hatakeyama, S, Ishihara, J,, Takahashi, K,, Imai, N,, Tsurumoto, J,, Onyango, EO   +5 more
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Time Economy in Total Synthesis.

Journal of Organic Chemistry, 2020
It is often said that "time is money". This is certainly true in a multistep synthesis when a high-valued product or set of products is needed urgently. Fulfilling this need requires the sensible balancing of atom economy, step economy, and redox economy
Y. Hayashi
semanticscholar   +1 more source

Total Synthesis of Paecilomycine A.

ChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Sun-Joon Min, Samuel J. Danishefsky, Samuel J. Danishefsky   +2 more
openaire   +5 more sources

Total Synthesis of Auripyrone A [PDF]

Angewandte Chemie, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Lister, Troy, Perkins, Michael Victor
openaire   +4 more sources

Toward Total Synthesis of Thiolate-Protected Metal Nanoclusters.

Accounts of Chemical Research, 2018
Total synthesis, where desired organic- and/or biomolecules could be produced from simple precursors at atomic precision and with known step-by-step reactions, has prompted centuries-lasting bloom of organic chemistry since its conceptualization in 1828 (
Qiaofeng Yao, Tiankai Chen, Xun Yuan, Jianping Xie   +3 more
semanticscholar   +1 more source

Total Synthesis of Siomycin A: Completion of the Total Synthesis

Chemistry – An Asian Journal, 2008
AbstractThe total synthesis of siomycin A (1), a representative compound of the thiostrepton family of peptide antibiotics, was achieved by incorporating the five synthetic segments A (2), B (3), C (4), D (5), and E (6). The dehydropiperidine segment A (2) was esterified with the dihydroquinoline segment C (4), and the subsequent coupling with the β ...
Taiji Goto, Tomonori Mori, Shuhei Higashibayashi, Masaya Nakata, Yukiko Satouchi, Mitsunori Kohno, Shunya Suzuki, Kengo Suzuki, Kazuyuki Shinko, Hiraku Tohmiya, Kimiko Hashimoto, Kimiko Hashimoto   +11 more
openaire   +3 more sources

Divergent Strategy in Natural Product Total Synthesis.

Chemical Reviews, 2018
The divergent total syntheses of complex natural products from a common intermediate have attracted enormous attention in the chemical community in the past few years because it can improve the efficiency of chemical synthesis.
Lei Li, Zhuang Chen, Xiwu Zhang, Yanxing Jia   +3 more
semanticscholar   +1 more source

Total Synthesis of (+)‐Alstonlarsine A

Angewandte Chemie, 2022
AbstractAn enantioselective total synthesis of (+)‐alstonlarsine A (1), a monoterpenoid indole alkaloid possessing a unique pentacyclic skeleton as well as a rare biological activity, is achieved. The key step is an efficient domino sequence, comprising enamine formation followed by an inverse‐electron‐demand intramolecular dearomative Diels–Alder ...
Zorana Ferjancic, Andrej Kukuruzar, Filip Bihelovic   +2 more
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Recent advances in the application of Diels-Alder reactions involving o-quinodimethanes, aza-o-quinone methides and o-quinone methides in natural product total synthesis.

Chemical Society Reviews, 2018
In recent decades, transient and highly reactive ortho-quinodimethanes (o-QDMs), ortho-quinone methides (o-QMs) and aza-ortho-quinone methides (aza-o-QMs) have attracted much attention and have been extensively studied and applied in organic synthesis ...
Baochao Yang, Shuanhu Gao
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Furan Oxidation Reactions in the Total Synthesis of Natural Products

Synthesis, 2018
Recent developments on the transformations of furans under oxidative conditions toward the total synthesis of complex natural compounds are discussed. Reactions and methods are classified according to the type of oxidant used.
A. Makarov, M. Uchuskin, I. Trushkov
semanticscholar   +1 more source