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cycloaddition

Also contains definition of: dipolar cycloaddition

A reaction in which two or more unsaturated molecules (or parts of the same molecule) combine with the formation of a cyclic adduct in which there is a net reduction of the bond multiplicity. The following two systems of notations have been used for the more detailed specification of cycloadditions, of which the second, more recent system [described under (2)] is preferred:
  1. A(i + j + ...) cycloaddition is a reaction in which two or more molecules (or parts of the same molecule), respectively, provide units of i, j, ... linearly connected atoms: these units become joined at their respective termini by new σ-bonds so as to form a cycle containing (i + j + ...) atoms. In this notation, (a) a Diels–Alder reaction is a (4+2) cycloaddition, (b) the initial reaction of ozone with an alkene is a (3+2) cycloaddition, and (c) the reaction shown below is a (2+2+2) cycloaddition. (N.B.: parentheses (...) are used in the description based on numbers of atoms.)
    C01496-1
  2. The symbolism [i + j + ...] for a cycloaddition identifies the numbers i, j, ... of electrons in the interacting units that participate in the transformation of reactants to products. In this notation the reaction (a) and (b) of the preceding paragraph would both be described as [2+4] cycloadditions, and (c) as a [2+2+2] cycloaddition. The symbol a or s (a = antarafacial, s = suprafacial) is often added (usually as a subscript after the number to designate the stereochemistry of addition to each fragment. A subscript specifying the orbitals, viz. σ, π (sigma, pi) with their usual significance) or n (for an orbital associated with a single atom only), may be added as a subscript before the number. Thus the normal Diels–Alder reaction is a [ 4 s + 2 s ] or [ 4 s π + 2 s π ] cycloaddition, whilst the reaction:
    C01496-2
    would be a [ 14 a + 2 s ] or [ 14 a π + 2 s π ] cycloaddition. (N.B. Square brackets [...] are used in the descriptions based on numbers of electrons.) Cycloadditions may be pericyclic reactions or (non-concerted stepwise reactions . The term 'dipolar cycloaddition' is used for cycloadditions of 1,3-dipolar compounds.
Source:
PAC, 1994, 66, 1077 (Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)) on page 1103
InChI=1/C7H8/c1-2-7-4-3-6(1)5-7/h1-4,6-7H,5H2
SJYNFBVQFBRSIB-UHFFFAOYAK
InChI=1/C6H6O4/c1-9-5(7)3-4-6(8)10-2/h1-2H3
VHILMKFSCRWWIJ-UHFFFAOYAX
InChI=1/C13H14O4/c1-16-12(14)10-8-5-3-4-6(8)7(4)9(5)11(10)13(15)17-2/h4-9H,3H2,1-2H3
YZQAUJSISPRMIU-UHFFFAOYAH
InChI=1/C14H12/c1-2-6-10-13(9-5-1)14-11-7-3-4-8-12-14/h1-12H
CJRANKZVJIECNW-UHFFFAOYAK
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IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. doi:10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: doi:10.1351/goldbook.C01496.
Original PDF version: http://www.iupac.org/goldbook/C01496.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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