✦ LIBER ✦

Diastereofacial control in the Lewis acid catalyzed cyclocondensation reaction of aldehydes with activated dienes: a synthesis of the Mus musculus pheromone

✍ Scribed by Danishefsky, Samuel J.; Pearson, William H.; Harvey, Daniel F.

Book ID: 126117874
Publisher: American Chemical Society
Year: 1984
Tongue: English
Weight: 263 KB
Volume: 106
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00320a050

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

On the relationship of topological and d

On the relationship of topological and diastereofacial control in the Lewis acid catalyzed cyclocondensation reaction of alkoxyaldehydes with activated dienes: metal tunable asymmetric induction

✍ Danishefsky, Samuel J.; Pearson, William H.; Harvey, Daniel 📂 Article 📅 1984 🏛 American Chemical Society 🌐 English ⚖ 360 KB

Stereochemical consequences of the Lewis

Stereochemical consequences of the Lewis acid catalyzed cyclocondensation of oxygenated dienes with aldehydes. A rapid and stereoselective entry to various natural products derived from propionate

✍ Danishefsky, Samuel; Kato, Nobuo; Askin, David; Kerwin, James F. 📂 Article 📅 1982 🏛 American Chemical Society 🌐 English ⚖ 394 KB

Reaction of Optically Active α-Aminoalle

Reaction of Optically Active α-Aminoallenylstannanes with Aldehydes Formed in situ from the Lewis Acid Catalyzed Rearrangement of Epoxides.

✍ Cristobal de los Rios; Louis S. Hegedus 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

Reaction of Optically Active α-Aminoalle

Reaction of Optically Active α-Aminoallenylstannanes with Aldehydes Formed in Situ from the Lewis-Acid-Catalyzed Rearrangement of Epoxides

✍ de los Ríos, Cristóbal; Hegedus, Louis S. 📂 Article 📅 2005 🏛 American Chemical Society 🌐 English ⚖ 90 KB

Lewis acid catalysis in micellar systems

Lewis acid catalysis in micellar systems. Sc(OTf)3-Catalyzed aqueous aldol reactions of silyl enol ethers with aldehydes in the presence of a surfactant

✍ Shū Kobayashi; Takeshi Wakabayashi; Satoshi Nagayama; Hidekazu Oyamada 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 183 KB

Scandium triflate (Sc(OTf)3)-catalyzed aldol reactions of silyl enol ethers with aldehydes were successfully carried out in micellar systems. While the reactions proceeded sluggishly in water, remarkable enhancement of the reactivity was observed in the presence of a small amount of a surfactant. In

ChemInform Abstract: Lewis Acid Catalysi

ChemInform Abstract: Lewis Acid Catalysis in Micellar Systems. Sc(OTf)3-Catalyzed Aqueous Aldol Reactions of Silyl Enol Ethers with Aldehydes in the Presence of a Surfactant.

✍ S. KOBAYASHI; T. WAKABAYASHI; S. NAGAYAMA; H. OYAMADA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views