✦ LIBER ✦

A Facile Route to Acyclic Substituted α,β-Unsaturated Aldehydes: The Allene Claisen Rearrangement

✍ Scribed by Parsons, Philip J.; Thomson, Peter; Taylor, Andrew; Sparks, Timothy

Book ID: 120809101
Publisher: American Chemical Society
Year: 2000
Tongue: English
Weight: 58 KB
Volume: 2
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol990305m

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Facile Route to A

ChemInform Abstract: A Facile Route to Acyclic Substituted α,β-Unsaturated Aldehydes: The Allene Claisen Rearrangement.

✍ Philip J. Parsons; Peter Thomson; Andrew Taylor; Timothy Sparks 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

A Facile Route to Glyoxal Mono(diethyl A

A Facile Route to Glyoxal Mono(diethyl Acetal): A Versatile Synthon for Preparation of α,β-Unsaturated Aldehydes

✍ Babler, James H. 📂 Article 📅 1987 🏛 Taylor and Francis Group 🌐 English ⚖ 280 KB

Selenosulfonation of allenes and subsequ

Selenosulfonation of allenes and subsequent rearrangement of the adducts: A facile synthetic route to β-arylsulfonyl-substituted allylic alcohols

✍ Young-Hee Kang; John L. Kice 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 94 KB

A new method for the bishomologation of

A new method for the bishomologation of carbonyl compounds to α,β-unsaturated aldehydes via the [3,3]sigmatropic rearrangement of allylic thionocarbamates

✍ Takeshi Nakai; Tetsuya Mimura; Akira Ari-Izumi 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 220 KB

The aldol condensation continues to play a fundamental role in organic synthesis and many methods have recently been developed for directing the aldol condensation of nonidentical carbonyl partners.2) A novel approach to the directed aldol condensation involves a two-carbon

A facile route to N-acetyl α,β-unsaturat

A facile route to N-acetyl α,β-unsaturated γ-lactam derivatives using ethyl acetamidocyanoacetate and dialkyl acetylenedicarboxylate in the presence of triphenylphosphine

✍ Sakineh Asghari; Mahmood Tajbakhsh; Vali Taghipour 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 118 KB

Michael addition of ethyl acetoacetate t

Michael addition of ethyl acetoacetate to α,β-unsaturated oximes in the presence of FeCl3: a novel synthetic route to substituted nicotinic acid derivatives

✍ Andrey M Chibiryaev; Norbert De Kimpe; Alexey V Tkachev 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 69 KB

The FeCl 3 -catalyzed reaction of a,b-unsaturated oximes with ethyl acetoacetate resulted in Michael addition followed by ring closure to produce substituted nicotinic acid derivatives in a very efficient way.