Published in Synthesis 3, 227-255, 1998
which should be used for any reference to this work 1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
Tandem Reactions Combining Diels-Alder Reactions with Sigmatropic Rearrangement Processes and their Use in Synthesis
29
0
0
Texte intégral
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
(15)
(16)
(17)
(18)
(19)
(20)
(21)
(22)
(23)
(24)
(25)
(26)
(27)
(28)
(29)
Documents relatifs
❑ Interpréter les résultats cinétiques, stéréochimiques et la régiosélectivité d’une réaction de Diels-Alder sous contrôle cinétique orbitalaire.. ❑ Identifier
In conclusion, we have developed an efficient organocatalytic enantioselective Diels-Alder reaction of unbiased quinones with thiodienecarbamates using a SPINOL
The investigation of the Diels-A ider reactions involving cyclopentadiene and its substituted analogs in Chapter 4 involved two main objectives: the examination of the e
In connection with our involvement in the study of in ver se electron demand Diels-Alder (IEDDA) reactions, electron deficient dienes 9a and lOa were prepared
ABSTRACT: We report herein the synthesis of complex molecules containing furopyran cores through a gold(I)-catalyzed hetero Diels-Alder cascade reaction.. During this process,
Hetero-Diels-Alder reactions of new sulfonylsulfines generated from alpha-substituted methylsulfones
When in the substrates (i.e. 5a-c) the sulfonyl group and the second substituent on the methylene carbon have comparable electronwithdrawing effect, a mixture of cis and trans
In summary after selection of a target DA reaction, several strategies have been followed to prepare artificial enzymes which can be divided into two main
As depicted in Scheme 4, the domino reaction of a range of , -unsaturated aldehydes 2 with methyl propargylcyanoacetate 13 performed at room temperature in toluene as the
