✦ LIBER ✦

A common and stereoselective strategy for the synthesis of N,O,O,O-tetra-acetyl d-ribo-(2S,3S,4R)-phytosphingosine and 2-epi-jaspine B

✍ Scribed by G. Srinivas Rao; B. Venkateswara Rao

Book ID: 113929732
Publisher: Elsevier Science
Year: 2011
Tongue: French
Weight: 429 KB
Volume: 52
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2011.07.032

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A common strategy for the stereoselectiv

A common strategy for the stereoselective synthesis of anhydrophytosphingosine pachastrissamine (jaspine B) and N,O,O,O-tetra-acetyl d-lyxo-phytosphingosine

✍ G. Srinivas Rao; B. Venkateswara Rao 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 431 KB

Synthesis of 1,2,3,4-tetra-O-acetyl-5-de

Synthesis of 1,2,3,4-tetra-O-acetyl-5-deoxy-5-C-[(R) and (S)-methoxyphosphinyl]-α- and -β-d-ribopyranoses

✍ Hiroshi Yamamoto; Masahiko Harada; Saburo Inokawa; Kuniaki Seo; Margaret-Ann Arm 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 534 KB

## Treatment of methyl 5-deoxy-S-C-(diethoxyphosphinyl)-2.3-O-isopropylidene-p-D-ribofuranoside with sodium dihydrobis(2-methoxyethoxy)aluminate, followed by hydrogen peroxide, mineral acid, and hydrogen peroxide, gave 5deoxy-5-C-(hydroxyphosphinyl)-a,P-D-ribopyranoses in 40-45% overall yield. The

Synthesis of 1,2,3,4-tetra-O-acetyl-5-de

Synthesis of 1,2,3,4-tetra-O-acetyl-5-deoxy-5-C-[(R)- and (S)-isopropylphosphinyl]-α- and -β-d-xylopyranose

✍ Kuniaki Seo 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 312 KB

Synthesis of 1,2,3,4-tetra-O-acetyl-5-de

Synthesis of 1,2,3,4-tetra-O-acetyl-5-deoxy-5-C-[(R)- and (S)-isopropylphosphinyl]-α- and -β-d-ribopyranose

✍ Kuniaki Seo 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 278 KB

Synthesis of 1,2,3,4-tetra-O-acetyl-5-de

Synthesis of 1,2,3,4-tetra-O-acetyl-5-deoxy-5-C-[(R)- and (S)-phenylphosphinyl]-α- and -β-d-ribopyranose

✍ Kuniaki Seo; Mitsuji Yamashita 📂 Article 📅 1986 🏛 Elsevier Science 🌐 English ⚖ 386 KB

Synthesis and the structural analysis of

Synthesis and the structural analysis of 1,2,3,4-tetra-O-acetyl-5-deoxy-5-C-[(R,S)-methoxyphosphinyl]-α,β-d-xylopyranoses

✍ Hiroshi Yamamoto; Tadashi Hanaya; Saburo Inokawa; Mitsuji Yamashita; Margaret-An 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 219 KB

Various sugar analogs possessing a phosphorus atom in the hemiacetal ring have been preparedIe because of the interest in their physicochemical properties and also the potential utility of'their biological activity. Compared with a large number of the analogs having an alkyl-or aryl-phosphinyl group