✦ LIBER ✦

Pictet-Spengler reactions of epinephrine with formaldehyde and acetaldehyde

✍ Scribed by Bates, Hans Aaron

Book ID: 115456764
Publisher: American Chemical Society
Year: 1981
Tongue: English
Weight: 727 KB
Volume: 46
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00337a022

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Characterization of tetrahydroisoquinoli

Characterization of tetrahydroisoquinolines produced by Pictet-Spengler reactions of norepinephrine with formaldehyde and acetaldehyde

✍ Bates, Hans Aaron 📂 Article 📅 1983 🏛 American Chemical Society 🌐 English ⚖ 504 KB

Effect of pH on the regioselectivity of

Effect of pH on the regioselectivity of Pictet-Spengler reactions of 3-hydroxyphenethylamines with formaldehyde and acetaldehyde

✍ Bates, Hans A.; Bagheri, Kourosh; Vertino, Paula M. 📂 Article 📅 1986 🏛 American Chemical Society 🌐 English ⚖ 441 KB

Identification of 4-methylspinaceamine -

Identification of 4-methylspinaceamine - a Pictet – Spengler condensation reaction product of histamine with acetaldehyde - in human urine

✍ Takeshi Ohya; Masaru Niitsu 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 254 KB

Stereoselectivity of Superacid-Catalyzed

Stereoselectivity of Superacid-Catalyzed Pictet—Spengler Cyclization Reactions.

✍ Satoshi Nakamura; Masaru Tanaka; Tooru Taniguchi; Masanobu Uchiyama; Tomohiko Oh 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 128 KB 👁 2 views

Pictet–Spengler reactions of oxetan-3-on

Pictet–Spengler reactions of oxetan-3-ones and related heterocycles

✍ Beasley, Benjamin O.; Alli-Balogun, Abimbola; Clarkson, Guy J.; Shipman, Michael 📂 Article 📅 2014 🏛 Elsevier Science 🌐 French ⚖ 377 KB

Synthesis of optically pure pyrroloquino

Synthesis of optically pure pyrroloquinolones via Pictet–Spengler and Winterfeldt reactions

✍ Weiqin Jiang; Zhihua Sui; Xin Chen 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 256 KB

Diastereomers of substituted 2,3,4,9-tetrahydro-1H-b-carbolines were synthesized via asymmetric Pictet-Spengler reaction of the chiral tryptamine derived from R-1-naphthalen-1-yl-ethylamine with 67% of d.e. The S,R-b-carboline can be converted to the R,R form by treating with TFA. Optically pure pyr