ChemInform Abstract: Radical Anellation Reactions of Allyl Iodomalononitriles.
Identifieur interne : 001501 ( Istex/Corpus ); précédent : 001500; suivant : 001502ChemInform Abstract: Radical Anellation Reactions of Allyl Iodomalononitriles.
Auteurs : D. P. Curran ; C. M. SeongSource :
- ChemInform [ 0931-7597 ] ; 1992-07-28.
English descriptors
- KwdEn :
- Achiral, Achiral precursors, Allyl, Allyl iodomalononitriles, Anellation, Anellation procedure, Atom transfer, Chem, Closure, Corresponding reactions, Curran, Cyclization, Cyclization step, Cyclopentanes, Iodomalononitriles, Nitrile, Nitrile transfer reaction, Precursor, Propargyl, Propargyl iodomalononitriles, Radical anellation reactions, Reductive, Reductive cyclization, Regioselectivity, Ring closure reactions ring closure reactions, Seong, Several cases, Stereogenic, Stereogenic centers, Suitable precursors, Tetrahedron, Univ.
- Teeft :
- Achiral, Achiral precursors, Allyl, Allyl iodomalononitriles, Anellation, Anellation procedure, Atom transfer, Chem, Closure, Corresponding reactions, Curran, Cyclization, Cyclization step, Cyclopentanes, Iodomalononitriles, Nitrile, Nitrile transfer reaction, Precursor, Propargyl, Propargyl iodomalononitriles, Radical anellation reactions, Reductive, Reductive cyclization, Regioselectivity, Ring closure reactions ring closure reactions, Seong, Several cases, Stereogenic, Stereogenic centers, Suitable precursors, Tetrahedron, Univ.
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Url:
DOI: 10.1002/chin.199230072
Links to Exploration step
ISTEX:5B4DC9CC99D621DA4203DAD6EBAAD31989A812BDLe document en format XML
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