Tetrahedron Letters

Electronic nature of the aza substituent of pyridyl and quinolyl groups for reactivities in an insulated system

M Sawada, M Ichihara, T Ando, Y Yukawa, Y Tsuno

Index: Tetrahedron Letters, , vol. 21, p. 4917 - 4920

Full Text: HTML

Citation Number: 2

Abstract

... Tetrahedron Letters. Volume 21, Issue 51, 1980, Pages 4917–4920. Cover image Cover image. Electronic nature of the aza substituent of pyridyl and quinolyl groups for reactivities in an insulated system ☆. ... References. 2); P. Tomasik, CD Johnson; ...

Related Articles:

Preparation, characterization and use of 1, 3-disulfonic acid imidazolium hydrogen sulfate as an efficient, halogen-free and reusable ionic liquid catalyst for the …

[Journal of Molecular Catalysis A: Chemical, , vol. 365, p. 15 - 23]

Reduction with polymer-bound nadh models.

[Tetrahedron Letters, , vol. 23, # 49 p. 5141 - 5144]

Highly efficient system for reduction of carboxylic acids and their derivatives to alcohols by HfCl4/KBH4

[Synthetic Communications, , vol. 39, # 9 p. 1640 - 1654]

Novel and facile selective reduction of carboxylic acid with a samarium diiodide–lanthanide triflate–methanol–base system

[Tetrahedron Letters, , vol. 41, # 3 p. 341 - 344]

N-Methylpyrrolidine-zinc borohydride: As a new stable and efficient reducing agent in organic synthesis

[Synthetic Communications, , vol. 33, # 2 p. 229 - 236]

More Articles...