✦ LIBER ✦

Synthesis of chiral disubstituted 18-crown-6-ethers with C2symmetry from D-sorbitol

✍ Scribed by É. P. Serebryakov; R. I. Abylgaziev; E. A. Él'perina; M. I. Struchkova

Book ID: 112544368
Publisher: Springer
Year: 1986
Tongue: English
Weight: 47 KB
Volume: 35
Category: Article
ISSN: 1573-9171
DOI: 10.1007/bf01474244

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chiral complexing agents and phase-trans

Chiral complexing agents and phase-transfer agents Communication 2. Synthesis of disubstituted 18-crown-6 ethers with C2symmetry starting from D-sorbitol

✍ É. P. Serebryakov; R. I. Abylgaziev; E. A. Él'perina; M. I. Struchkova 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 482 KB

Synthesis of New Chiral Diaza 18-Crown-6

Synthesis of New Chiral Diaza 18-Crown-6 Ethers from Chiral Amines.

✍ N. Demirel; Y. Turgut; H. Hosgoeren 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 71 KB 👁 2 views

ChemInform Abstract: Synthesis of New Ch

ChemInform Abstract: Synthesis of New Chiral 18-Crown-6 Ethers from D-Xylose.

✍ G. V. M. Sharma; V. Goverdhan Reddy; Palakodety Radha Krishna 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

Chiral recognition properties of chiral

Chiral recognition properties of chiral 18-crown-6 ethers with aromatic substituents

✍ Junzo Yamashita; Hideaki Takahashi; Harukichi Hashimoto; Keiichi Kitahara; Hisao 📂 Article 📅 1984 🏛 Springer Netherlands 🌐 English ⚖ 399 KB

Chiral complex formers and agents for tr

Chiral complex formers and agents for transphase transfer. Communication 3. Synthesis of podands with C2symmetry and 24-crown-8-ether with D2symmetry derived from from 1,4; 3,6-dianhydro-D-mannitol

✍ E. A. Él'perina; R. I. Abylgaziev; M. I. Struchkova; É. P. Serebryakov 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 518 KB

Synthesis of Substituted Crown-Ethers by

Synthesis of Substituted Crown-Ethers by radical addition of 18-crown-6

✍ Ju. B. Zeleconok; V. V. Orlovskij; Prof. Dr. S. S. Zlotskij; Prof. Dr. D. L. Rac 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 238 KB

## Abstract An example of the synthesis of substituted crown‐ethers by radical addition reaction of 18‐crown‐6 (1) to several α‐olefins (2a‐e), cyclohexene (2f), vinyl butyl ether (2g), allyl alcohol (2h), trimethylvinylsilane (2i), diethylmaleate (2j) and formaldehyde (2k) in the presence of a per