Results 171 to 180 of about 15,108 (230)

Association of three different dietary patterns with the metabolomic profiles of children: the BiomarKid project. [PDF]

Eur J Nutr
Gheorghita I, Vehovec L, Grote V, Horak J, Gispert-Llauradó M, Ferré N, Koletzko B, Demmelmair H, Kratochwill K, Verduci E, Gruszfeld D, Escribano J, Kastenmüller G, Luque V.   +13 more
europepmc   +1 more source

Crustal structure of La Palma Island inferred from 3D aeromagnetic modelling. [PDF]

Sci Rep
Romero-Toribio MC, Martín-Hernández F, Ledo J.   +2 more
europepmc   +1 more source

Analyses of the Ss and Slp proteins in a hemolytic assay for murine C41.

Immunobiology, 1981
J P, Atkinson, K M, McGinnis, J, Peterein, D C, Shreffler   +3 more
openaire   +1 more source

MSXプリント・アート入門 : カラープロッタープリンターPRN-C41

, 1984
openaire   +1 more source

Research reports on information sciences series C:Computer science C41

, 1981
openaire   +1 more source

C41-C122

, 2007
exaly   +3 more sources

Synthesis of the C28–C41 Side Chain of (Proposed) Neaumycin B: A Contiguous Stereohextet

Organic Letters, 2023
The C28-C41 side-chain of the proposed structure of neaumycin B, which encompasses a contiguous stereohextet, is prepared in 8 steps (longest linear sequence). Convergency is maximized via Williams' Felkin-Anh-selective triorganozincate-mediated vinylation of an α,β-stereogenic aldehyde. The relative stereochemical assignment of the C33-C35 stereotriad
Da Seul Lee, Saki Maejima, Michael J. Krische   +2 more
openaire   +3 more sources

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Diastereoselective synthesis of the C29–C41 fragment of karlotoxin 2

Tetrahedron Letters, 2015
A highly diastereoselective synthesis of the C29–C41 fragment of karlotoxin 2 (KmTx2) is described by employing regio-selective epoxide opening, our own developed domino isomerization followed by C–O and C–C bond formation reaction and chelation-controlled Grignard reaction as key steps.
Nagaraju Devunuri, Debendra Mohapatra
exaly   +2 more sources

Stereoselective Synthesis of the C31–C41 Spirolactam Fragment of Sanglifehrin A

European Journal of Organic Chemistry, 2013
AbstractA stereoselective synthesis of the spirolactam fragment (C31–C41) of a highly‐potent immunosuppressant sanglifehrin A is described. The key steps involved in this synthesis are a desymmetrization protocol, Sharpless asymmetric epoxidation, Crimmins syn aldol reaction, Barton–McCombie deoxygenation, and acid‐mediated spirolactamization.
Debendra Mohapatra
exaly   +2 more sources

C41

2023
exaly   +2 more sources