✦ LIBER ✦

A stereocontrolled synthesis of (2R,3R,5R,13S,14R)- (+)-Aplidiasphingosine, a marine terpenoid

✍ Scribed by Kenji Mori; Takeaki Umemura

Publisher: Elsevier Science
Year: 1982
Tongue: French
Weight: 246 KB
Volume: 23
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)87623-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: First Stereocontrol

ChemInform Abstract: First Stereocontrolled Synthesis of the (3S,5R,7R,10R,11R)-C1—C13 Fragment of Nystatin A1.

✍ Guy Solladie; Nicole Wilb; Claude Bauder; Carlo Bonini; Licia Viggiani; Lucia Ch 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Cyclic dipeptides. A stereocontrolled sy

Cyclic dipeptides. A stereocontrolled synthesis of (2S,3R,6R)- and (2R,3R,6R)-6-tert-butoxycarbonylamino-3-methoxycarbonyl-2-methyl-5-oxoperhydro-1,4-thiazepine

✍ Federico Corelli; Angela Crescenza; Donata Dei; Maurizio Taddei; Maurizio Botta 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 228 KB

Synthesis of a Prenylated and Immunosupp

Synthesis of a Prenylated and Immunosuppressive Marine Galactosphingolipid with Cyclopropane-Containing Alkyl Chains: (2S,3R,11S,12R,2′′′R,5′′′Z,11′′′S,12′′′R)-Plakoside A and Its (2S,3R,11R,12S,2′′′R,5′′′Z,11′′′R,12′′′S) Isomer

✍ Masanori Seki; Kenji Mori 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 536 KB

The synthesis of polyhydroxylated amino

The synthesis of polyhydroxylated amino acids from glucuronolactone: enantiospecific syntheses of 2s, 3r, 4r, 5s-trihydroxypipecolic acid, 2r, 3r, 4r, 5s-trihydroxypipecolic acid and 2r, 3r, 4r-dihydroxyproline

✍ Bharat P. Bashyal; Hak-Fun Chow; Linda E. Fellows; George W.J. Fleet 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 643 KB

Synthesis of (2S,3R,11S,12R,2‴R,11‴S,12‴

Synthesis of (2S,3R,11S,12R,2‴R,11‴S,12‴R)-plakoside A, a prenylated and immunosuppressive marine galactosphingolipid with cyclopropane-containing alkyl chains

✍ Masanori Seki; Akihiro Kayo; Kenji Mori 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 92 KB

Plakoside A (1) is a prenylated galactosphingolipid isolated from the marine sponge Plakortis simplex and is strongly immunosuppressive without cytotoxicity. (2S,3R,11S,12R,2 §R,11 §S,12 §R)-plakoside A (1) was synthesized by combining sphingosine part 16, a-hydroxy acid part 24 and prenylated sugar

Synthesis of [2-13C, 4-13C]-(2R,3S)-cate

Synthesis of [2-13C, 4-13C]-(2R,3S)-catechin and [2-13C, 4-13C]-(2R,3R)-epicatechin

✍ Pradeep K. Sharma; Min He; Leo J. Romanczyk Jr; Hagen Schroeter 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 French ⚖ 196 KB 👁 1 views

## Abstract The first synthesis of doubly labeled, [2‐^13^C, 4‐^13^C]‐(2__R__,3__S__)‐catechin 15 and [2‐^13^C, 4‐^13^C]‐(__2R__,3__R__)‐epicatechin 18 starting from labeled 2‐hydroxy‐4, 6‐bis(benzyloxy)acetophenone 3 and labeled 3, 4‐bis(benzyloxy)‐benzaldehyde 7 are described. Copyright © 2010 Jo