✦ LIBER ✦

The EANM Physics Committee celebrates its first 5

Publisher: Springer
Year: 2011
Tongue: English
Weight: 129 KB
Volume: 38
Category: Article
ISSN: 0340-6997
DOI: 10.1007/s00259-011-1859-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The EANM Scientific Pillars — the EANM p

The EANM Scientific Pillars — the EANM proudly presents its 11 Committees

📂 Article 📅 2009 🏛 Springer 🌐 English ⚖ 574 KB

REMCO, the ISO Council Committee on Refe

REMCO, the ISO Council Committee on Reference Materials – its first 25 years

✍ Michael Parkany; Harry Klich; S. Rasberry 📂 Article 📅 2001 🏛 Springer-Verlag 🌐 English ⚖ 60 KB

Physical and crystallographic characteri

Physical and crystallographic characterisation of the mGlu5 antagonist MTEP and its monohydrochloride

✍ Matthew J. McIldowie; Michael N. Gandy; Brian W. Skelton; Jonathan M. Brotchie; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 389 KB

ChemInform Abstract: The First Synthesis

ChemInform Abstract: The First Synthesis of a Novel 5:7:5-Fused Diimidazodiazepine Ring System and Some of Its Chemical Properties.

✍ Raj Kumar; Ravi K. Ujjinamatada; Ramachandra S. Hosmane 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

ChemInform Abstract: The First Enantiose

ChemInform Abstract: The First Enantioselective Total Synthesis of Cyclomyltaylane-5α-ol and Determination of Its Absolute Stereochemistry.

✍ Hisahiro Hagiwara; Hitoshi Sakai; Takashi Uchiyama; Yoshiaki Ito; Noriyuki Morit 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 2 views

The first stereo selective total synthes

The first stereo selective total synthesis of (3R),(5R)-5-hydroxy-de-O-methyllasiodiplodin and its epimer via an RCM protocol

✍ J.S. Yadav; Saibal Das; J. Satyanarayana Reddy; N. Thrimurtulu; A.R. Prasad 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 314 KB

The first total synthesis of (3R),(5R)-5-hydroxy-de-O-methyllasiodiplodin and its epimer is reported from malic acid. The adopted approach is highly convergent and stereoselective. The strategy utilizes syn selective reduction and ring-closing metathesis as key steps.