✦ LIBER ✦

Highly Diastereoselective Conjugate Addition of Lithium Dialkylamides to α,β-Unsaturated Esters Having a Chiral Center at the γ-Position

✍ Scribed by Asao, Naoki; Shimada, Takashi; Sudo, Tomoko; Tsukada, Naofumi; Yazawa, Kazuhiko; Gyoung, Young Soo; Uyehara, Tadao; Yamamoto, Yoshinori

Book ID: 120481985
Publisher: American Chemical Society
Year: 1997
Tongue: English
Weight: 572 KB
Volume: 62
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo970435d

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Highly Diastereosel

ChemInform Abstract: Highly Diastereoselective Conjugate Addition of Lithium Dialkylamides to α,β-Unsaturated Esters Having a Chiral Center at the γ-Position.

✍ N. ASAO; T. SHIMADA; T. SUDO; N. TSUKADA; K. YAZAWA; Y. S. GYOUNG; T. UYEHARA; Y 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 42 KB 👁 1 views

Diastereoface Selectivity During Pthalim

Diastereoface Selectivity During Pthalimidonitrene Additions to (E)-and (Z)-configurated α, β-unsaturated esters, induced by a chiral center in the γ-position

✍ Zdzislaw Chilmonczyk; Markus Egli; Christoph Behringcr; AndréS. Dreiding 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 German ⚖ 755 KB

On leave of absence from Pharmaceutical Institute, Warszawa-Poland. Partially from the diploma thesis of C. B., University of

Highly Selective Addition of Chiral, Sul

Highly Selective Addition of Chiral, Sulfonimidoyl Substituted Bis(allyl)titanium Complexes to N -Sulfonyl α-Imino Esters: Asymmetric Synthesis of γ,δ-Unsaturated α-Amino Acids Bearing a Chiral, Electron-Withdrawing Nucleofuge at the δ-Position

✍ Schleusner, Marcel; Gais, Hans-Joachim; Koep, Stefan; Raabe, Gerhard 📂 Article 📅 2002 🏛 American Chemical Society 🌐 English ⚖ 185 KB

Conjugate addition of lithium ester enol

Conjugate addition of lithium ester enolates to 1-chlorovinyl p-tolyl sulfoxides: a novel synthesis of functionalized esters and lactones having a tertiary or a quaternary carbon at the β-position

✍ Tsuyoshi Satoh; Shimpei Sugiyama; Yuhki Kamide; Hiroyuki Ota 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 258 KB

Addition of the lithium ester enolates to 1-chlorovinyl p-tolyl sulfoxides, which were synthesized from chloromethyl p-tolyl sulfoxide and ketones or aldehydes, gave esters having a tertiary or a quaternary carbon at the 3-position, and chlorine and sulfinyl groups at the 4-position in high to quant

Conjugate Addition of Lithium Ester Enol

Conjugate Addition of Lithium Ester Enolates to 1-Chlorovinyl p-Tolyl Sulfoxides: A Novel Synthesis of Functionalized Esters and Lactones Having a Tertiary or a Quaternary Carbon at the β-Position.

✍ Tsuyoshi Satoh; Shimpei Sugiyama; Yuhki Kamide; Hiroyuki Ota 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 168 KB 👁 2 views