✦ LIBER ✦

Approach to Geminally Alkylated Azaphthalans via a Consecutive Double Desilylation—Alkylation Reaction: Application to a Synthesis of Cerpegin.

✍ Scribed by Tarun K. Sarkar; Sankar Basak

Book ID: 101964304
Publisher: John Wiley and Sons
Year: 2004
Weight: 18 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200450116

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Application of Seco

ChemInform Abstract: Application of Secondary Alkyl Halides to a Domino Aryl Alkylation Reaction for the Synthesis of Aromatic Heterocycles.

✍ Alena Rudolph; Nils Rackelmann; Marc-Olivier Turcotte-Savard; Mark Lautens 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 48 KB 👁 2 views

ChemInform Abstract: A General Approach

ChemInform Abstract: A General Approach to High-Yielding Asymmetric Synthesis of Chiral 3-Alkyl-4-nitromethylchromans via Cascade Barbas—Michael and Acetalization Reactions.

✍ Dhevalapally B. Ramachary; M. Shiva Prasad; R. Madhavachary 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 49 KB 👁 2 views

ChemInform Abstract: A Stereoselective A

ChemInform Abstract: A Stereoselective Approach to 6-Alkylated Piperidinone & 2-Piperidine via Three-Component Vinylogous Mannich Reactions (VMR) and a Concise Synthesis of (S)-Anabasine.

✍ Yang Yang; Dean P. Phillips; Shifeng Pan 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

A Flexible Approach to (S)-5-Alkyl Tetra

A Flexible Approach to (S)-5-Alkyl Tetramic Acid Derivatives: Application to the Asymmetric Synthesis of (+)-Preussin and Protected (3S,4S)-AHPPA.

✍ Pei-Qiang Huang; Tian-Jun Wu; Yuan-Ping Ruan 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 142 KB 👁 2 views

Nitroalkanes as Alkyl Anion Synthons — A

Nitroalkanes as Alkyl Anion Synthons — A New Approach to the Synthesis of 2-SubstitutedN-Ethyl Succinimides and 2-Substituted Succinate Diesters via Nitroalkanes

✍ Ballini, Roberto ;Bosica, Giovanna 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 256 KB

## Abstract 2‐Substituted __N__‐ethyl succinimide and 2‐substituted succinate diesters were obtained by two key steps: (i) Michael addition of a nitroalkane to the appropriate enedione derivative under basic conditions (DBU), with the concomitant elimination of nitrous acid, and (ii) selective redu

Enantioselective synthesis of 2-benzylox

Enantioselective synthesis of 2-benzyloxy alcohols and 1,2-diols via alkylation of chiral glycolate imides. A convenient approach to optically active glycerol derivatives

✍ Giuliana Cardillo; Mario Oren; Marta Romero; Sergio Sandri 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 460 KB