✦ LIBER ✦

Revision of the absolute stereochemistry of ilimaquinone

✍ Scribed by Capon, Robert J.; MacLeod, John K.

Book ID: 127091826
Publisher: American Chemical Society
Year: 1987
Tongue: English
Weight: 278 KB
Volume: 52
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00231a051

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Revised Relative and Absolute Stereochem

Revised Relative and Absolute Stereochemistry of (+)-Purpurin

✍ Pirrung, Michael C.; Lee, Yong Rok; Morehead, Andrew T.; McPhail, Andrew T. 📂 Article 📅 1998 🏛 American Chemical Society 🌐 English ⚖ 59 KB

(-)-Cryptaustoline: its synthesis, revis

(-)-Cryptaustoline: its synthesis, revision of absolute stereochemistry, and mechanism of inversion of stereochemistry

✍ Meyers, A. I.; Sielecki, Thais M.; Crans, Debbie C.; Marshman, Robert W.; Nguyen 📂 Article 📅 1992 🏛 American Chemical Society 🌐 English ⚖ 937 KB

Revised Structure of Tetrapetalone A and

Revised Structure of Tetrapetalone A and Its Absolute Stereochemistry.

✍ Toshikazu Komoda; Yasumasa Sugiyama; Naoki Abe; Misako Imachi; Hiroshi Hirota; H 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 85 KB 👁 1 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

On the stereochemistry of coronatine : r

On the stereochemistry of coronatine : revised absolute configuration of (+)-coronamic acid

✍ Akitami Ichihara; Kunio Shiraishi; Sadao Sakamura; Ako Furusaki; Nobuhiro Hashib 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 195 KB

In the previous paper, we reported the stereochemistry of coronatine 1) , in which amino acid part, (+) -coronamic acid, was described as the enantiomer ofA on the basis of application of sector rule. 3) In this communication, we would like to describe further investigation on the stereochemistry of

Synthesis of detoxininolactone derivativ

Synthesis of detoxininolactone derivatives and the revised absolute stereochemistry of detoxinine

✍ Katsumi Kakinuma; Noboru Ōtake; Hiroshi Yonehara 📂 Article 📅 1980 🏛 Elsevier Science 🌐 French ⚖ 132 KB

First stereoselective synthesis of synar

First stereoselective synthesis of synargentolide A and revision of absolute stereochemistry

✍ Gowravaram Sabitha; Peddabuddi Gopal; C. Nagendra Reddy; J.S. Yadav 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 337 KB

The first stereoselective total synthesis of synargentolide A isolated from Syncolostemon argenteus has been achieved from commercially available (R)-benzyl glycidyl ether using Sharpless asymmetric epoxidation and cross-metathesis reactions as the key steps. Comparing the spectral data of the synth