LEADER 02179nam  2200397z- 450 
001 9910557713003321
005 20231214133138.0
035   $a(CKB)5400000000046195
035   $a(oapen)https://directory.doabooks.org/handle/20.500.12854/73736
035   $a(EXLCZ)995400000000046195
100   $a20202111d2020      |y             0
101 0 $aeng
135   $aurmn|---annan
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 10$aGreen Synthesis of Heterocycles
210   $cFrontiers Media SA$d2020
215   $a1 electronic resource (95 p.)
311   $a2-88963-584-8 
330   $aHeterocycles are among the most common scaffolds in many organic molecules, e.g., vitamins, hormones, antibiotics, alkaloids, herbicides, dyes, drugs, and pharmaceutically relevant substances. These molecules are also incorporated in numerous macromolecules such as DNA, polymers, and macrocycles, where their hetero-functional units are often employed to establish supramolecular interaction. It is thus not surprising that?since the 19th century?the synthesis of heterocycles has been constantly blooming, evolving from classic condensation reactions to the development of click reactions and new multicomponent domino synthetic approaches. In the last thirty years, with the ever-growing research developments of new and atom-efficient sustainable synthetic strategies, the field of Green Chemistry has made significant contributions to the development of heterocyclic motifs. The novel methodologies aim at high process performances by means of eco-compatible methodologies, employing non-toxic and biodegradable chemicals.
606   $aScience: general issues$2bicssc
610   $agreen chemistry
610   $aheterocycles
610   $acyclic compound
610   $asustainable
610   $agreen principles
615  7$aScience: general issues
700   $aArico$b Fabio$4edt$01328964
702   $aReiser$b Oliver$4edt
702   $aArico$b Fabio$4oth
702   $aReiser$b Oliver$4oth
906   $aBOOK
912   $a9910557713003321
996   $aGreen Synthesis of Heterocycles$93039233
997   $aUNINA