Light‐Driven Diselenide Metathesis in Peptides
نویسندگان
چکیده
منابع مشابه
Structural and pharmacological effects of ring-closing metathesis in peptides.
Applications of ring-closing alkene metathesis (RCM) in acyclic α- and β-peptides and closely related systems are reviewed, with a special emphasis on the structural and pharmacological effects of cyclization by RCM.
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Heptapeptides containing residues with terminal olefin-derivatized side chains (3 and 4) have been treated with ruthenium alkylidene 1 and undergone facile ring-closing olefin metathesis (RCM) to give 21- and 23-membered macrocyclic peptides (5 and 6). The primary structures of peptides 3 and 4 were based upon a previously studied heptapeptide (2), which was shown to adopt a predominantly 3(10)...
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The title mol-ecule, C(10)H(6)O(4)Se(2), lies on a twofold rotation axis. The Se-Se bond length of 2.305 (3) Å is similar to that in diphenyl diselenide [2.3066 (7) and 2.3073 (10) Å for the P and M isomers, respectively] and longer than that in 1,8-diseleno-naph-thalene [2.0879 (8) Å]. The mol-ecule adopts a gauche conformation with respect to the C=O groups.
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Ruthenium and molybdenum catalysts are widely used in synthesis of both small molecules and macromolecules. While major developments have led to new increasingly active catalysts that have high functional group compatibility and stereoselectivity, catalyst/product separation, catalyst recycling, and/or catalyst residue/product separation remain an issue in some applications of these catalysts. ...
متن کاملCrystal structure of dibenzoyl diselenide.
C14H10O2Se2 is monoclinic, P2(1)/c. The unit-cell dimensions at 293 K are a = 12.795(2), b = 12.126(2), c = 9.0179(13)A, beta = 107.074(6)degrees, V = 1337.5(3)A3, and Z = 4. The R value is 0.048 for 2319 observed reflections. The dihedral angle between the plane C4-C7(O2)-Se1 and C9-C8(O1)-Se2 is 85.6(2)degrees, keeping the Se atom unshared electron pairs in a more stable configuration with th...
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ژورنال
عنوان ژورنال: ChemistryOpen
سال: 2019
ISSN: 2191-1363,2191-1363
DOI: 10.1002/open.201900224