Tetrahedron Letters 2018-04-07

Synthesis of benzyl halide derivatives of spirohydantoins via [2+2+2] cyclotrimerization reaction

Sanbasivarao Kotha, Gaddamedi Sreevani

Index: 10.1016/j.tetlet.2018.04.012

Full Text: HTML

Abstract

Generally, synthesis of hydantoin derivatives involve use of carbonyl compounds which in turn require multistep synthesis. Here, we report a new approach to assemble spirohydantoins via [2+2+2] cyclotrimerization reaction using commercially available, inexpensive hydantoin as a starting material.

Latest Articles:

A BODIPY-bearing pillar[5]arene for mimicking photosynthesis: multi-fluorophoric light harvesting system

2018-04-11

[10.1016/j.tetlet.2018.04.016]

A Highly Diastereoselective Chloride-Mediated Dynamic Kinetic Resolution at Phosphorus On-Route to a Key Intermediate in the Synthesis of GSK2248761A

2018-04-11

[10.1016/j.tetlet.2018.04.018]

Efficient Suzuki-Miyaura mono-arylation of symmetrical diiodo(hetero)arenes

2018-04-10

[10.1016/j.tetlet.2018.04.015]

Microwave promoted reaction of purin-6-yl magnesium halides with aldehydes in dichloromethane at 100 °C

2018-04-10

[10.1016/j.tetlet.2018.04.014]

Synthesis of functionalized iodoalkenes using a multicomponent reaction triggered by electrophilic iodination of alkenyldiazoacetates

2018-04-04

[10.1016/j.tetlet.2018.03.063]

More Articles...