✦ LIBER ✦

Formation and Cleavage of Bisnoradamantane Derivatives Through SmI2 Reductions.

✍ Scribed by Pelayo Camps; Andres E. Lukach; Santiago Vazquez

Publisher: John Wiley and Sons
Year: 2010
Weight: 29 KB
Volume: 32
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200129089

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Preparation of 2-Aminobenzophenones and

Preparation of 2-Aminobenzophenones and Polysubstituted Quinolines Through SmI2 Promoted Reductive Cleavage of 3-Aryl-2,1-benzisoxazoles.

✍ Xuesen Fan; Xinying Zhang; Yongmin Zhang 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 23 KB 👁 1 views

Preparation of 2-aminobenzophenones and

Preparation of 2-aminobenzophenones and polysubstituted quinolines through SmI2 promoted reductive cleavage of 3-aryl-2,1-benzisoxazoles

✍ Xuesen Fan; Xinying Zhang; Yongmin Zhang 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 108 KB

## Abstract Promoted by SmI~2~, 3‐aryl‐2,1‐benzi‐ soxazoles underwent reductive cleavage of the NO bond leading to 2‐aminobenzophenones in high yields upon protonation. Otherwise, if ketones with active methylene group were added to the reaction mixture prior to protonation, the desired polysubsti

Reductive cleavage of NO bonds in hydro

Reductive cleavage of NO bonds in hydroxylamine and hydroxamic acid derivatives using SmI2/THF

✍ Gary E. Keck; Stanton F. McHardy; Travis T. Wager 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 227 KB

Formation and Cleavage of Dihydroxydiary

Formation and Cleavage of Dihydroxydiarylmethane Derivatives

✍ Dr. H. Schnell; Dr. H. Krimm 📂 Article 📅 1963 🏛 John Wiley and Sons 🌐 English ⚖ 814 KB

Diastereoselective reduction and carbon

Diastereoselective reduction and carboncarbon bond formation of α-keto esters/amides with SmI2

✍ Shin-ichi Fukuzawa; Manabu Miura; Hiroshi Matsuzawa 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 70 KB

The stereoselective reduction of a-keto esters/a-keto amides, which have various chiral auxiliaries using SmI 2 , is examined. 2(S)-Methoxymethylpyrrolidine, 1,1,2(S)-and 1,1,2(R)-triphenylethanediol were found to be suitable chiral auxiliaries that produced the corresponding a-hydroxy ester and ami

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Reduction and Carbon—Carbon Bond Formation of α-Keto Esters/Amides with SmI2.

✍ Shin-ichi Fukuzawa; Manabu Miura; Hiroshi Matsuzawa 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v