✦ LIBER ✦

Studies in aza-Claisen rearrangement: synthesis of dimedone-annelated unusual heterocycles

✍ Scribed by K.C. Majumdar; S.K. Samanta

Book ID: 108371215
Publisher: Elsevier Science
Year: 2001
Tongue: French
Weight: 96 KB
Volume: 57
Category: Article
ISSN: 0040-4020
DOI: 10.1016/s0040-4020(01)00405-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Studies in Aza-Clai

ChemInform Abstract: Studies in Aza-Claisen Rearrangement: Synthesis of Dimedone-Anellated Unusual Heterocycles.

✍ K. C. Majumdar; S. K. Samanta 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

Studies on Sulfoxide Rearrangement: Synt

Studies on Sulfoxide Rearrangement: Synthesis of Dimedone-Anellated Heterocycles.

✍ K. C. Majumdar; S. K. Samanta 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Studies on Pyrimidine-Annelated Heterocy

Studies on Pyrimidine-Annelated Heterocycles: Synthesis of Pyrrolo[3,2- d ]pyrimidines by Amine Oxide Rearrangement

✍ Majumdar, K. C.; Das, U.; Jana, N. K. 📂 Article 📅 1998 🏛 American Chemical Society 🌐 English ⚖ 127 KB

Synthetic and Mechanistic Studies of the

Synthetic and Mechanistic Studies of the Aza-Retro-Claisen Rearrangement. A Facile Route to Medium Ring Nitrogen Heterocycles

✍ Boeckman, Robert K.; Genung, Nathan E.; Chen, Ke; Ryder, Todd R. 📂 Article 📅 2010 🏛 American Chemical Society 🌐 English ⚖ 231 KB

ChemInform Abstract: Synthesis of Azepin

ChemInform Abstract: Synthesis of Azepine- and Azocine-Annulated Heterocycles by Aromatic Aza-Claisen Rearrangement and Ring-Closing Metathesis.

✍ K. C. Majumdar; Srikanta Samanta; Buddhadeb Chattopadhyay; Raj Kumar Nandi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Synthesis of spiro-sesquiterpenes in the

Synthesis of spiro-sesquiterpenes in the vetivane series via an aza-claisen rearrangement

✍ Patrick M. McCurry Jr.; Rajendra K. Singh 📂 Article 📅 1973 🏛 Elsevier Science 🌐 French ⚖ 181 KB

We wish to report a version of the aae&Xaisen rearrangement1 whioh should prove useful in the preparation of dlastereomerio apiro oompounds. Speoifioally, we have applied this method in the total syntheeis of Spiro-sesquiterpenee (i-) S-vet&one (Ia)? (+) 10-epi-0-vetivone2b( Ib), and (k) R-vetiapire