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Books on the topic 'Conjugate addition'

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Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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1

Begum, Adiba. Conjugate addition approaches to secondary difluoromethylphosphonates. Birmingham: University of Birmingham, 1998.

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2

Perlmutter, P. Conjugate addition reactions in organic synthesis. Oxford: Pergamon, 1992.

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3

Reed, Darrell. Conjugate addition of lithium reagents to y-oxygenated a,b-unsaturated ketoesters. Salford: University of Salford, 1994.

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4

Vicario, Jose L. Organocatalytic enantioselective conjugate addition reactions: A powerful tool for the stereocontrolled synthesis of complex molecules. Cambridge: Royal Society of Chemistry, 2010.

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5

Manage, Ajith Chandersiri. Stereoselective conjugate additions of a-sulphinyl carbanions. Salford: University of Salford, 1991.

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6

Walker, Andrew J. Conjugate additions of sulphoxide-stabilised carbanions: Scope and applications. Salford: University of Salford, 1991.

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7

Organocatalytic Enantioselective Conjugate Addition Reactions. Cambridge: Royal Society of Chemistry, 2010. http://dx.doi.org/10.1039/9781849732185.

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8

Conjugate Addition Reactions in Organic Synthesis. Elsevier, 1992. http://dx.doi.org/10.1016/c2009-0-11165-0.

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9

Perlmutter, Patrick. Conjugate Addition Reactions in Organic Synthesis. Elsevier, 2020.

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10

Perlmutter, P., and Patrick Perlmutter. Conjugate Addition Reactions in Organic Synthesis. Elsevier Science & Technology Books, 2013.

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11

Perlmutter, Patrick. Conjugate Addition Reactions in Organic Synthesis. Elsevier, 2022.

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12

Baldwin, Ian Craig. New methodology involving allylic substitution and conjugate addition reactions. 1996.

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13

Jaw, John-Yan. Charge-directed conjugate addition reactions and their applications to the construction of carbocycles. 1986.

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14

Whitehead, Christopher R. Application of a new two-step conjugate addition-anodic oxidation strategy in a synthetic approach to the cyathane diterpenes. 2003.

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15

Mann, Peter. The Hamiltonian & Phase Space. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198822370.003.0014.

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Abstract:

This chapter discusses the Hamiltonian and phase space. Hamilton’s equations can be derived in several ways; this chapter follows two pathways to arrive at the same result, thus giving insight into the motivation for forming these equations. The importance of deriving the same result in several ways is that it shows that, in physics, there are often several mathematical avenues to go down and that approaching a problem with, say, the calculus of variations can be entirely as valid as using a differential equation approach. The chapter extends the arenas of classical mechanics to include the cotangent bundle momentum phase space in addition to the tangent bundle and configuration manifold, and discusses conjugate momentum. It also introduces the Hamiltonian as the Legendre transform of the Lagrangian and compares it to the Jacobi energy function.

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16

Pollock, Charles Morgan. I. Deprotonation of and nucleophilic additions to iron [beta]-oxoalkyl complexes ; II. Charge-directed conjugate additions to [alpha]-silylated-[alpha], [beta]-unsaturated amides. 1989.

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