Enantioselective aldol chemistry via alkyl enol ethers. Scope of the Lewis acid catalyzed condensation of optically active trimethylsilyl and methyl 2-[(E)-1-alkenyloxy]ethanoates with acetals

DOI: 10.1021/ja00009a029

Source and publish data:

Journal of the American Chemical Society p. 3418 - 3426 (1991)

Update date:2022-09-26

Topics:

Authors:

Faunce, James A.

Grisso, Bryan A.

Mackenzie, Peter B.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/ja00009a029

Optically active, mono- and disubstituted trimethylsilyl 2-[(E)-1-alkenyloxy]ethanoates of the type RR¹CH = CHOCHR²CO₂SiMe₃ (R = Me, PhCH₂, n-Bu, MeO₂CCMe₂CH₂, PhSCH View More

Full text of DOI:10.1021/ja00009a029

Products guided by the article

Product name:2-benzyl-1,1,3-trimethoxybutane

Cas No:133797-58-7

R&D Labs maybe for 133797-58-7

BIOS CHEMICALS

Contact:+33-5-34012600

Address:28 ZA des Pignès
Anhui Eapearl Chemical Co., Ltd.

Contact:86-562-5858458

Address:358 South Huaihe Road
Xi'an North Information Industry Co., Ltd. Weilv Chemical Department

Contact:+86-29-88156413

Address:Jixiang Road 99 Xi'an Shaanxi Province
ANHUI CHEM-BRIGHT BIOENGINEERING CO.,LTD

Contact:86-561-4080321

Address:No.8 Lieshan Industrial Zone of Huaibei
HANGZHOU PANYU CHEMICAL CO.,LIMITED

Contact:+86-571-86578491

Address:Rm 605, NO.1870 Binsheng Road,Binjiang Dist, Hangzhou, China

Relevant to this article

Synthesis and biological evaluation of new opioid agonist and neurokinin-1 antagonist bivalent ligands

Doi:10.1016/j.bmc.2011.08.027
(2011)
Doi:10.1139/v56-188
(1956)
Doi:10.1021/jo01284a025
(1967)
Enantioselective syntheses of (+)-sertraline and (+)-indatraline using lithiation/borylation-protodeboronation methodology

Doi:10.1021/ol202251p
(2011)
Synthesis of new imidazole derivatives as potential inhibitors of thromboxane synthetase. II

Doi:10.1002/jhet.5570280237
(1991)
Electrochemical generation and reactions of acyloxytriphenylphosphonium ions

Doi:10.1016/S0040-4020(01)87066-6
(1991)

Article Doi