✦ LIBER ✦

Reaction of γ-Sultines with Electrophilic Reagents. Part 1. Bromination of 3,5-Diaryl-1,2-oxathiolane 2-Oxides.

✍ Scribed by E. V. Grigor'ev; L. G. Saginova

Publisher: John Wiley and Sons
Year: 2003
Weight: 95 KB
Volume: 34
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200339082

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reactions of γ-Sultines with Electrophil

Reactions of γ-Sultines with Electrophilic Reagents. Part 2. Bromination of 3,5-Diaryl-1,2-oxathiolane 2-Oxides in the Presence of Lewis Acids.

✍ E. V. Grigor'ev; L. G. Saginova 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 106 KB 👁 1 views

Reactions of γ-Sultines with Electrophil

Reactions of γ-Sultines with Electrophilic Reagents. Part 3. Chlorination of 3,5-Diaryl-1,2-oxathiolane 2-Oxides.

✍ E. V. Grigor'ev; L. G. Saginova; I. Yu. Kleimenova 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 127 KB 👁 1 views

Reactions of γ-Sultines with Electrophil

Reactions of γ-Sultines with Electrophilic Reagents. Part 4. Chlorination of 5-(4-Methoxyphenyl)-3-phenyl-1,2-oxathiolane 2-Oxide.

✍ E. V. Grigor'ev; L. G. Saginova; I. Yu. Kleimenova 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 145 KB 👁 1 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Reactions of 2,3-Diaryl-1-methyl-4,5-dih

Reactions of 2,3-Diaryl-1-methyl-4,5-dihydroimidazolium Iodides with Nucleophilic Reagents.

✍ Chizhong Xia; Junsheng Hao; Yiqing Tang; Yanping Ni; Peiwen Zhou 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: Reaction of 3,5-Bis

ChemInform Abstract: Reaction of 3,5-Bis(4-methoxyphenyl)-1,2-oxathiolane-2-oxide with Phosphorus Trichloride

✍ E. V. Grigor'ev; L. G. Saginova 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

Reaction of 1,3-Thiazole-5(4H)-thiones w

Reaction of 1,3-Thiazole-5(4H)-thiones with 1,2-Epoxycycloalkanes: Formation of Spirocyclic 1,3-Oxathiolanes

✍ Milen Blagoev; Anthony Linden; Heinz Heimgartner 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 German ⚖ 168 KB 👁 1 views

Treatment of solutions of 1,3-thiazole-5(4H)-thiones 1 in CH 2 Cl 2 at room temperature with BF 3 ´Et 2 O and 1,2-epoxycyclohexane (7-oxabicyclo[4.1.0]heptane; 2a) or 1,2-epoxycyclopentane (6-oxabicyclo[3.1.0]hexane; 2b) yielded mixtures of diastereoisomeric spirocyclic 1,3-oxathiolanes (3/4 and 8/9