Sources of common compounds: 97739-46-3

In addition to the literature in the link below, there is a lot of literature about this compound(1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane)Product Details of 97739-46-3, illustrating the importance and wide applicability of this compound(97739-46-3).

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 97739-46-3, is researched, SMILESS is CC1(C2)OC(C3)(C)OC2(C)OC3(C)P1C4=CC=CC=C4, Molecular C16H21O3PJournal, Article, Research Support, Non-U.S. Gov’t, Journal of Organic Chemistry called Development of methods for the synthesis of libraries of substituted maleimides and α,β-unsaturated-γ-butyrolactams, Author is Awuah, Emelia; Capretta, Alfredo, the main research direction is diarylmaleimide preparation; dibromomaleimide arylboronic acid Suzuki coupling palladium; diaminomaleimide preparation; amine dibromomaleimide amination; diarylbutyrolactam preparation.Product Details of 97739-46-3.

Synthetic methods for the preparation of maleimide and α,β-unsaturated-γ-butyrolactam compound collections are described. These routes take advantage of Pd cross-coupling and conjugate addition/elimination reactions to permit the facile production of bisaryl-maleimides, anilinoaryl-maleimides, and bisanilino-maleimides while allowing control over the synthesis of sym. or nonsym. derivatives Similarly, the chem. developed allows for the generation of bisaryl substituted α,β-unsaturated-γ-butyrolactams. The scope and limitations of the approaches are presented.

In addition to the literature in the link below, there is a lot of literature about this compound(1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane)Product Details of 97739-46-3, illustrating the importance and wide applicability of this compound(97739-46-3).

Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics