𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Synthesis and Biological Evaluation of 6,6-Spiroketal Natural Products: Reveromycin A, B and Spirofungin A, B

✍ Scribed by Takeshi Shimizu

Publisher
John Wiley and Sons
Year
2009
Weight
15 KB
Volume
40
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Enantioselective Sy
ChemInform Abstract: Enantioselective Synthesis of the [6,6] Spiroketal Core (I) of Reveromycin A (II).
✍ Keith E. Drouet; Taotao Ling; Hung V. Tran; Emmanuel A. Theodorakis πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 26 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: Synthesis of the Sp
ChemInform Abstract: Synthesis of the Spiroacetal Parts of Spirofungin A and B.
✍ Yuko Shimizu; Hiromasa Kiyota; Takayuki Oritani πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 32 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: Enantioselective To
ChemInform Abstract: Enantioselective Total Synthesis of Reveromycin B.
✍ Keith E. Drouet; Emmanuel A. Theodorakis πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 1 views

Enantioselective Total Synthesis of Reveromycin B. -The crucial steps to synthesize the title compound (VIII) include a modified Negishi coupling of alkyne (I) with iodide (II) and the Kishi-Nozaki coupling of aldehyde (IV) with iodide (V). The former coupling is more efficient and superior as compa