✦ LIBER ✦

ChemInform Abstract: Boulton—Katritzky Rearrangement

✍ Scribed by Michael T. Corbett; Richard J. Mullins

Book ID: 112044091
Publisher: John Wiley and Sons
Year: 2012
Weight: 18 KB
Volume: 43
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201219232

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Boulton-Katritzky R

ChemInform Abstract: Boulton-Katritzky Rearrangement of 5-(Cyanoimino)-1,2,4-thiadiazolines.

✍ H. SONNENSCHEIN; E. SCHMITZ; E. GRUENDEMANN; E. SCHROEDER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

ChemInform Abstract: The Boulton—Katritz

ChemInform Abstract: The Boulton—Katritzky Rearrangement of Isocarboxazid.

✍ Susan D. Van Arnum; Henry J. Niemczyk 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 KB

ChemInform Abstract: Synthetic Studies T

ChemInform Abstract: Synthetic Studies Toward 3-(Acylamino)-1H-indazoles and Development of a One-Pot, Microwave-Assisted, Oxadiazole Condensation/Boulton—Katritzky Rearrangement.

✍ Gregory R. Ott; Andrew V. Anzalone 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 34 KB

The Boulton–Katritzky rearrangement of i

The Boulton–Katritzky rearrangement of isocarboxazid

✍ Susan D. Van Arnum; Henry J. Niemczyk 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 78 KB

## Abstract magnified image Isocarboxazid rearranges on heating to 5‐acetonyl‐2‐benzyl‐4‐hydroxy‐1,2,3‐triazole in DMF at 150°C, in the ionic liquid, [bmin]HSO at 100°C or as a melt at 105°C. This is the first reported example of the Boulton–Katritzky rearrangement of an acyl hydrazide. J. Heteroc

Comprehensive Organic Name Reactions and

Comprehensive Organic Name Reactions and Reagents || Boulton-Katritzky Rearrangement

✍ Wang, Zerong 📂 Article 📅 2010 🏛 John Wiley & Sons, Inc. ⚖ 128 KB

Boulton-Katritzky Rearrangement of 5-(cy

Boulton-Katritzky Rearrangement of 5-(cyanoimino)-1,2,4-Thiadiazolines

✍ Sonnenschein, Helmut ;Schmitz, Ernst ;Gründemann, Egon ;Schröder, Edith 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 376 KB

## Abstract The products of the addition of nucleophiles (alcohols, amines) to the cyano group of 5‐(cyanoimino)thiadiazolines 1 undergo a Boulton‐Katritzky rearrangement. The thiadiazoles 4 are formed by subsequent nitrile elimination. In the case of bicyclic thiadiazoloazepine 5 an equilibrium mi