✦ LIBER ✦

Chiral Bornadiene: Its Synthesis and Rearrangement

✍ Scribed by Prof. Dr. M. R. Willcott III; Dr. C. J. Boriack

Book ID: 101546193
Publisher: John Wiley and Sons
Year: 1971
Tongue: English
Weight: 125 KB
Volume: 10
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.197100781

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chiral bornadiene. Its synthesis and cha

Chiral bornadiene. Its synthesis and characterization

✍ Willcott, M. Robert; Boriack, Clinton J. 📂 Article 📅 1971 🏛 American Chemical Society 🌐 English ⚖ 326 KB

Synthesis and biomimetic rearrangement o

Synthesis and biomimetic rearrangement of a chiral diterpene dioxide

✍ Thomas Lindel; Burchard Franck 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 257 KB

Synthesis of chiral crownophanes via tan

Synthesis of chiral crownophanes via tandem Claisen rearrangement

✍ Hideo Tokuhisa; Yoshinobu Nagawa; Hirotaka Uzawa; Kazuhisa Hiratani 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 245 KB

A synthetic route for crownophanes containing a chiral binaphthyl unit using tandem Claisen rearrangement is described to demonstrate the versatility of this approach. Molecular recognition by the resulting crownophane for butylurea is also investigated.

ChemInform Abstract: Synthesis of Chiral

ChemInform Abstract: Synthesis of Chiral Crownophanes via Tandem Claisen Rearrangement.

✍ Hideo Tokuhisa; Yoshinobu Nagawa; Hirotaka Uzawa; Kazuhisa Hiratani 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views

ChemInform Abstract: Development of Epox

ChemInform Abstract: Development of Epoxysilane Rearrangement and Its Application to Chirality Transfer

✍ Michiko Sasaki; Hidaka Ikemoto; Kei Takeda 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 15 KB 👁 1 views

A synthesis of 7-methoxycephalosporin an

A synthesis of 7-methoxycephalosporin and its novel rearrangement

✍ Yukio Sugimura; Yuji Iwano; Kimio Iino; Tokio Saito; Tetsuo Hiraoka 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 238 KB

Recently much effort has been directed towards the synthesis of 7-methoxycephalosporins because of the finding of the cephamycin group and their enhanced activity towards gram negative bacteria1'2'3). We also have studied and reported 4) some novel reactions for introducing a methoxy group at C7 po