๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthesis and absolute stereochemistry of (+)-adociaquinones A and B

โœ Scribed by Nobuyuki Harada; Tatsuo Sugioka; Tomomi Soutome; Norie Hiyoshi; Hisashi Uda; Takeo Kuriki

Book ID
108036236
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
126 KB
Volume
6
Category
Article
ISSN
0957-4166

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Absolute stereochemistry of penaresidins
Absolute stereochemistry of penaresidins A and B
โœ Jun'ichi Kobayashi; Masashi Tsuda; Jie-fei Cheng; Masami Ishibashi; Hirosato Tak ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 124 KB

Absolute stereochemistry at C-15 in penaresidins A (1) and B (2) was established to be S on the basis of I H NMR data of the tri-O-MTPA esters, indicating that the absolute configurations of 1 and 2 are 2S, 3R, 4S, 15S (1 and 2), and 16S (1).

Synthesis and absolute stereochemistry o
Synthesis and absolute stereochemistry of thysanone
โœ Christopher D. Donner; Melvyn Gill ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 172 KB

The structure and absolute stereochemistry of thysanone 3 , a fungal benzoisochromanquinone with potent human rhbzovirus 3C-protease #zhibitoo" activity, is established by the total synthesis of its antipode I from (S)-propylene oxide.