✦ LIBER ✦

Oxidative dehydrogenation of 3-Methyl-2-buten-1-ol in microreactors

✍ Scribed by Enhong Cao; Asterios Gavriilidis; William B. Motherwell

Book ID: 108085949
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 199 KB
Volume: 59
Category: Article
ISSN: 0009-2509
DOI: 10.1016/j.ces.2004.08.020

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Cyclization of 3-methyl-3-buten-1-ol

✍ U. G. Ibatullin; T. F. Petrushina 📂 Article 📅 1993 🏛 Springer US 🌐 English ⚖ 82 KB

Isobaric vapor–liquid equilibria of the

Isobaric vapor–liquid equilibria of the binary mixtures 2-methyl-3-buten-2-ol + ethanol and 2-methyl-3-buten-2-ol + 1-butanol

✍ Yi Lei; Haoran Li; Longhua Zhu; Shijun Han 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 156 KB

Uptake kinetics of 3-buten-1-ol, 4-pente

Uptake kinetics of 3-buten-1-ol, 4-penten-1-ol and 3-methyl-3-buten-1-ol into sulfuric acid solutions

✍ ZhiFang Xu; Ze Liu; MaoFa Ge; WeiGang Wang 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 635 KB

Kinetics of the reactions of Cl atoms wi

Kinetics of the reactions of Cl atoms with 2-buten-1-ol, 2-methyl-2-propen-1-ol, and 3-methyl-2-buten-1-ol as a function of temperature

✍ Diana Rodriguez; Ana Rodriguez; Amparo Soto; Alfonso Aranda; Yolanda Diaz-de-Mer 📂 Article 📅 2008 🏛 Springer Netherlands 🌐 English ⚖ 194 KB

Synthese von 1-(6-Isopropyliden-3-methyl

Synthese von 1-(6-Isopropyliden-3-methyl-3-cyclohexen-1-yl)-2-methyl-3-buten-2-ol („Humbertiol”)

✍ Hoppmann, Angela ;Weyerstahl, Peter 📂 Article 📅 1974 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 336 KB 👁 1 views

## Abstract Umsetzung von 4‐Methyl‐1,4‐cyclohexadien‐1‐carbonsäure‐methylester (**(2)** mit Methyllithium führt zum tertiären Alkohol **3**, der zum Vinyläther **4** umgesetzt wird. __Claisen__‐Umlagerung von **4** gibt den Aldehyd **5**, der mit CH~3~MgJ zum sekundären Alkohol **6** reagiert. Oxid

A convenient preparation of 3-[2H3]methy

A convenient preparation of 3-[2H3]methyl-3-buten-1-ol

✍ Rudolph Ernst K. Winter; Zhigang Jian 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 French ⚖ 267 KB 👁 1 views

## Abstract A procedure for the conversion of 3‐hydroxy‐3‐methylglutaric anhydride to methyl 3‐methyl‐3‐butenoate forms the basis for a convenient synthesis of 3‐[^2^H~3~]methyl‐3‐buten‐1‐ol.