𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

✍ Scribed by Yadav, J.S.; Reddy, P. Adi Narayana; Kumar, A. Suman; Prasad, A.R.; Reddy, B.V. Subba; Al Ghamdi, Ahmad Alkhazim

Book ID
122091228
Publisher
Elsevier Science
Year
2014
Tongue
French
Weight
511 KB
Volume
55
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Stereoselective synthesis of (2S,3S,4R,5
Stereoselective synthesis of (2S,3S,4R,5S)-proline-3,4,5-d3
✍ Makoto Oba; Tsutomu Terauchi; Jun Hashimoto; Tomohiro Tanaka; Kozaburo Nishiyama πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 French βš– 227 KB

A catalytic deuteration of protected 3,4-dehydro-L-proline using RuCI2(PPh3) 3 followed by RuO~-oxidation gave a 3,4-dideuterated L-pyroglutamic acid derivative which is considered to be a promising precursor for various deuterated amino acids. The present study demonstrates a stereoselective reduct

The first stereoselective total synthesi
The first stereoselective total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-Ξ±-pyranone and total synthesis of (2S,3R,5S)-(βˆ’)-2,3-dihydroxytetradecan-5-olide
✍ Gowravaram Sabitha; Sambit Nayak; M. Bhikshapathi; J.S. Yadav πŸ“‚ Article πŸ“… 2009 πŸ› Elsevier Science 🌐 French βš– 185 KB

The first total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-a-pyranone 1 and total synthesis of (2S,3R,5S)-(Γ€)-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