✦ LIBER ✦

A stereospecific total synthesis of (3R,5S,9S*)-gephyrotoxin 223AB

✍ Scribed by Nakagawa, Yumi; Stevens, Robert V.

Book ID: 126070103
Publisher: American Chemical Society
Year: 1988
Tongue: English
Weight: 405 KB
Volume: 53
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00244a006

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Stereospecific total synthesis of (.+-.)

Stereospecific total synthesis of (.+-.)-gephyrotoxin 223AB

✍ Iida, Hideo; Watanabe, Yohya; Kibayashi, Chihiro 📂 Article 📅 1985 🏛 American Chemical Society 🌐 English ⚖ 233 KB

A short total synthesis of (.+-.)-gephyr

A short total synthesis of (.+-.)-gephyrotoxin-223AB

✍ Broka, Chris A.; Eng, Kan K. 📂 Article 📅 1986 🏛 American Chemical Society 🌐 English ⚖ 430 KB

The stereoselective total synthesis of (

The stereoselective total synthesis of (3R,5R)-sonnerlactone and (3R,5S)-sonnerlactone

✍ Yadav, J.S.; Shiva Shankar, K.; Srinivas Reddy, A.; Subba Reddy, B.V. 📂 Article 📅 2012 🏛 Elsevier Science 🌐 French ⚖ 471 KB

ChemInform Abstract: Stereospecific Synt

ChemInform Abstract: Stereospecific Synthesis of (2S,4R)-(5,5,5-D3)Leucine.

✍ R. A. AUGUST; J. A. KHAN; C. M. MOODY; D. W. YOUNG 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB

Stereoselective total synthesis of 4-((3

Stereoselective total synthesis of 4-((3S,5R)-3,5-dihydroxynonadecyl)phenol

✍ Yadav, J.S.; Reddy, P. Adi Narayana; Kumar, A. Suman; Prasad, A.R.; Reddy, B.V. 📂 Article 📅 2014 🏛 Elsevier Science 🌐 French ⚖ 511 KB

The first stereoselective total synthesi

The first stereoselective total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-α-pyranone and total synthesis of (2S,3R,5S)-(−)-2,3-dihydroxytetradecan-5-olide

✍ Gowravaram Sabitha; Sambit Nayak; M. Bhikshapathi; J.S. Yadav 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 185 KB

The first total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-a-pyranone 1 and total synthesis of (2S,3R,5S)-(À)-2,3-dihydroxytetradecan-5-olide 2 have been achieved in five steps in a highly stereoselective manner using Maruoka allylation, olefin cross-metathesis, and Sharpless asymmetric dihydroxyla

A stereospecific total synthesis of (3R*,5S*,9S*)-gephyrotoxin 223AB

A stereospecific total synthesis of (3R,5S,9S*)-gephyrotoxin 223AB