✦ LIBER ✦

Stereoselective syntheses of trans- and cis-cinnamic acid esters from the phenylalanine derivatives.

✍ Scribed by Norio Takamura; Tomishige Mizoguchi; Shun-ichi Yamada

Publisher: Elsevier Science
Year: 1973
Tongue: French
Weight: 165 KB
Volume: 14
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)87166-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of β-Glycosyl Esters of cis-Cinnamic Acid and Its Derivatives Using Unprotected Glycosyl Donors.

✍ Kazumasa Matsuo; Keisuke Nishikawa; Mitsuru Shindo 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

Steric course and regioselectivity in th

Steric course and regioselectivity in the cycloadditions of diazoacetic ester to trans- and cis-cinnamic ester

✍ Peter Eberhard; Rolf Huisgen 📂 Article 📅 1971 🏛 Elsevier Science 🌐 French ⚖ 264 KB

Enzymatic production of the lignin precu

Enzymatic production of the lignin precursor trans-[U-14C]cinnamic acid from l-[U-14C]phenylalanine using l-phenylalanine ammonia-lyase

✍ Anthony L. Pometto III; Don L. Crawford 📂 Article 📅 1981 🏛 Elsevier Science 🌐 English ⚖ 229 KB

ChemInform Abstract: A Mild Procedure fo

ChemInform Abstract: A Mild Procedure for the Stereospecific Transformation of trans Cinnamic Acid Derivatives to cis β-Bromostyrenes.

✍ Sun Hee Kim; Han-Xun Wei; Steven Willis; Guigen Li 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

cis- and trans-2-methoxycyclopropyllithi

cis- and trans-2-methoxycyclopropyllithium: novel reagents for the stereoselective syntheses of trans-βγ-unsaturated aldehydes

✍ E.J. Corey; Peter Ulrich 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 251 KB

In connection with other projects we have been seeking a general route to m-(or 3 j3, Yunsaturated aldehydes, in both free and protected form, via a three carbon chain extension which is equivalent to a hypothetical Wittig process from the unknown reagent R3P=CHCH2CH0. We report here the successful

The highly diastereoselective palladium-

The highly diastereoselective palladium-catalyzed cyclizations. Stereoselective syntheses of cis and trans-disubstituted hydroxycyclopentanes

✍ Young-Ger Suh; Jae-Kyung Jung; Soon-Ai Kim; Dong-Yun Shin; Kyung-Hoon Min 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 215 KB

A new variant of palladium-catalyzed stereoselective cyclization has been developed. This process provides an excellent 1,2-diastereocontrol of two new stereogenic centers as well as 1,3asymmetric induction. In addition, desulfonylation of the cyclization product with retention of the initial stereo