𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Facile Synthesis of 2,3-Diiodonaphthalene and 2-Bromo-3-iodonaphthalene.

✍ Scribed by Jonas Hellberg; Fredrik Allared; Margit Pelcam

Publisher
John Wiley and Sons
Year
2003
Weight
82 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

📜 SIMILAR VOLUMES

ChemInform Abstract: 2-Bromo-3,3,3-trifl
ChemInform Abstract: 2-Bromo-3,3,3-trifluoropropene: A Facile Trifluoromethylacetylene Anion Synthon.
✍ A. R. KATRITZKY; M. QI; A. P. WELLS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB

2-Bromo-3,3,3-trifluoropropene: A Facile Trifluoromethylacetylene Anion Synthon. -Use of 2-bromo-3,3,3-trifluoropropene (I) provides a convenient and high yielding method to introduce a trifluoromethylethynyl moiety into a wide range of organic substrates (→ (III); 8 examples). -

Facile Synthesis of 2′-Deoxyisoguanosine
Facile Synthesis of 2′-Deoxyisoguanosine and Related 2′,3′-Dideoxyribonucleosides
✍ Frank Seela; Bert Gabler 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 German ⚖ 519 KB

## Abstract The 2′‐deoxyisoguanosine (1) was synthesized by a two‐step procedure from 2′‐deoxyguanosine (5). Amination of silylated 2′‐deoxyguanosine yielded 2‐amino‐2′‐deoxyadenosine (6) which was subjected to selective deamination of the 2‐NH~2~ group resulting in compound 1. Also 2′,3′‐dideoxyis

A facile synthesis of 2,3-azaisoindoline
A facile synthesis of 2,3-azaisoindoline
✍ Subas M. Sakya; Michel Van Den Berg; Kees Pouwer; John M. Humphrey; Christopher 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 358 KB

a b s t r a c t 2,3-Azaisoindoline (4) was prepared via reaction of dichloride 11 with 2,4-dimethoxybenzyl amine followed by deprotection with trifluoroacetic acid and triethylsilane. Isolation of the unstable 2,3-azaisoindoline 4 was facilitated by conversion to the bis-HCl salt.

A facile synthesis of 2,3-disubstituted
A facile synthesis of 2,3-disubstituted furo[2,3-b]pyridines
✍ Gregory L. Beutner; Jeffrey T. Kuethe; Nobuyoshi Yasuda 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 174 KB

In a three-step sequence starting from readily available starting materials, 2,3-carbon disubstituted furo[2,3-b]pyridines can be accessed in good yields and purity. Furo[2,3-b]pyridines bearing ester, amide and ketone groups at the 2-position can be prepared with a variety of aryl and alkyl groups