✦ LIBER ✦

Efficient Method for Synthesis of Angucyclinone Antibiotics via Gold-Catalyzed Intramolecular [4 + 2] Benzannulation: Enantioselective Total Synthesis of (+)-Ochromycinone and (+)-Rubiginone B 2

✍ Scribed by Sato, Kenichiro; Asao, Naoki; Yamamoto, Yoshinori

Book ID: 126079472
Publisher: American Chemical Society
Year: 2005
Tongue: English
Weight: 140 KB
Volume: 70
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo051444m

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Efficient Method for Synthesis of Angucy

Efficient Method for Synthesis of Angucyclinone Antibiotics via Gold-Catalyzed Intramolecular [4 + 2] Benzannulation: Enantioselective Total Synthesis of (+)-Ochromycinone (Ia) and (+)-Rubiginone B2 (Ib).

✍ Kenichiro Sato; Naoki Asao; Yoshinori Yamamoto 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 11 KB 👁 2 views

ChemInform Abstract: Short and Efficient

ChemInform Abstract: Short and Efficient Enantioselective Total Synthesis of Angucyclinone Type Antibiotics (+)-Rubiginone B2 and (+)-Ochromycinone.

✍ M. Carmen Carreno; Antonio Urbano; Claudio Di Vitta 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

An Efficient Domino Approach for the Syn

An Efficient Domino Approach for the Synthesis of Multisubstituted Pyrroles via Gold/Silver-Catalyzed Amination/Cycloisomerization of (Z)-2-En-4-yn-1-ols

✍ Yuhua Lu; Xiaoping Fu; Haoyi Chen; Xiangwei Du; Xueshun Jia; Yuanhong Liu 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 183 KB 👁 2 views

ChemInform Abstract: An Efficient Domino

ChemInform Abstract: An Efficient Domino Approach for the Synthesis of Multisubstituted Pyrroles via Gold/Silver-Catalyzed Amination/Cycloisomerization of (Z)-2-En-4-yn-1-ols.

✍ Yuhua Lu; Xiaoping Fu; Haoyi Chen; Xiangwei Du; Xueshun Jia; Yuanhong Liu 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 49 KB 👁 2 views

ChemInform Abstract: Highly Enantioselec

ChemInform Abstract: Highly Enantioselective Construction of the Key Azetidin-2-ones for the Synthesis of Carbapenem Antibiotics via Intramolecular C—H Insertion Reactions of α-Methoxycarbonyl-α-diazoacetamides Catalyzed by Chiral Dirhodium(II) Carboxylates.

✍ M. ANADA; N. WATANABE; S. HASHIMOTO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 42 KB 👁 2 views

Highly Enantioselective Construction of the Key Azetidin-2-ones for the Synthesis of Carbapenem Antibiotics via Intramolecular C-H Insertion Reactions of α-Methoxycarbonyl-α-diazoacetamides Catalyzed by Chiral Dirhodium(II) Carboxylates. -The title reaction of compounds (I) and (III) to afford bicy

Palladium-Catalyzed Heteroannulation Lea

Palladium-Catalyzed Heteroannulation Leading to Heterocyclic Structures with Two Heteroatoms: A Highly Convenient and Facile Method for a Totally Regio- and Stereoselective Synthesis of ( Z )-2,3-Dihydro-2-(ylidene)-1,4-benzo- and -naphtho[2,3- b ]dioxins †

✍ Chowdhury, Chinmay; Chaudhuri, Gopeswar; Guha, Subhadra; Mukherjee, Alok k.; Kun 📂 Article 📅 1998 🏛 American Chemical Society 🌐 English ⚖ 123 KB