✦ LIBER ✦

A novel Diels-Alder approach to hydroisoquinolines

✍ Scribed by Jack E. Baldwin; David R. Spring; Roger C. Whitehead

Publisher: Elsevier Science
Year: 1998
Tongue: French
Weight: 187 KB
Volume: 39
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(98)01043-0

No coin nor oath required. For personal study only.

✦ Synopsis

A synthetic approach to functionalised hydroisoquinoline rings, using dihydropyridinium ions as dienophiles in the Diels-Alder reaction, is described.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Novel Diels—Alder

ChemInform Abstract: A Novel Diels—Alder Approach to Hydroisoquinolines.

✍ J. E. BALDWIN; D. R. SPRING; R. C. WHITEHEAD 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

A diels-alder approach to functionalised

A diels-alder approach to functionalised cis-hydroisoquinolines

✍ Dennis de Oliveira Imbroisi; Nigel S. Simpkins 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 243 KB

A new substituted 5,6-dihydro-2(lH)-pyridinone participates in highly efficient Diels-Alder reactions to give functional&d cis-hydroisoquinolines suitable for natural product synthesis. The cis-hydroisoquinoline ring system constitutes an important part of natural products such as the indole alkalo

A novel Diels-Alder approach to carbapen

A novel Diels-Alder approach to carbapenems

✍ Richard Bayles; Anthony P. Flynn; Ronald H.B. Galt; Susan Kirby; Ralph W. Turner 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 231 KB

An inverse electron demand heter\*Diels-Alder reaction between 2-acylaminc+ methylen&-oxobutanoic acid derivatives (5land ketene acetals (61yields crystalline dihydropyrans, which are versatile intermediates in the synthesis of carbapenems. Synthetic carbapenem analogues related to thienamycin show

A Diels-Alder, retro-Diels-Alder approac

A Diels-Alder, retro-Diels-Alder approach to arcyriaflavin-A

✍ M.Manuel B. Marques; Ana M. Lobo; Sundaresan Prabhakar; Paula S. Branco 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 112 KB

2,2'-Bi-indolyl-3,3'-dithiete and maleimide participate in a [4 + 2] cycloaddition reaction to provide arcyriaflavin-A.

A Novel Diels—Alder Approach to Heavily

A Novel Diels—Alder Approach to Heavily Substituted Azasugars.

✍ Kamyar Afarinkia; Akmal Bahar; Judi Neuss 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 101 KB 👁 2 views

A Diels–Alder Approach to (−)-Ovalicin

✍ Konrad Tiefenbacher; Vladimir B. Arion; Johann Mulzer 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 126 KB 👁 1 views