✦ LIBER ✦

Total Synthesis of (+)-Grandifloracin by Iron Complexation of a Microbial Arene Oxidation Product

✍ Scribed by Palframan, Matthew J.; Kociok-Köhn, Gabriele; Lewis, Simon E.

Book ID: 125837785
Publisher: American Chemical Society
Year: 2011
Tongue: English
Weight: 799 KB
Volume: 13
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol201057r

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Photooxygenation of a Microbial Arene Ox

Photooxygenation of a Microbial Arene Oxidation Product and Regioselective Kornblum–DeLaMare Rearrangement: Total Synthesis of Zeylenols and Zeylenones

✍ Dr. Matthew J. Palframan; Dr. Gabriele Kociok-Köhn; Dr. Simon E. Lewis 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 507 KB

Valuable New Cyclohexadiene Building Blo

Valuable New Cyclohexadiene Building Blocks from Cationic η5-Iron–Carbonyl Complexes Derived from a Microbial Arene Oxidation Product

✍ Monika Ali Khan; Dr. Mary F. Mahon; Dr. John P. Lowe; Dr. Alan J. W. Stewart; Dr 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 998 KB

The first total synthesis of calbistrin

The first total synthesis of calbistrin A, a microbial product possessing multiple bioactivities

✍ Kuniaki Tatsuta; Manabu Itoh; Ryusuke Hirama; Nobuyuki Araki; Masayuki Kitagawa 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 282 KB

The octahydronaphthopyranone moiety is synthesized from methyl ~t-D-mannopyranoside through the intramolecular Diels-Alder reaction, and the tetmenedicarboxylic acid moiety is from the enzymatically prepared anti-compound. Both moieties were coupled to accomplish the total synthesis of calbistrin A

Hydrogen production by the redox of iron

Hydrogen production by the redox of iron oxide prepared by hydrothermal synthesis

✍ Hui Wang; Xiaojie Liu; Fei Wen 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 996 KB

ChemInform Abstract: The First Total Syn

ChemInform Abstract: The First Total Synthesis of Calbistrin A, a Microbial Product Possessing Multiple Bioactivities.

✍ K. TATSUTA; M. ITOH; R. HIRAMA; N. ARAKI; M. KITAGAWA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

2,6-Cyclolycopene-1,5-diol: Total synthe

2,6-Cyclolycopene-1,5-diol: Total synthesis of a naturally occurring oxidation product of lycopene

✍ Bruno Traber; Hanspeter Pfander 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 624 KB

2,6-Cyclolycopene-l,5-diol (3) was synthesized in 9 steps starting from ¢t-terpinyl acetate (11). This represents the first total synthesis of an oxidative metabolite of lycopene (2). The synthesis was performed according to a C~.s + C~o + Cm5 = C40 strategy using the Wittig olefination to couple th