Organoaluminum-Promoted Rearrangement of Epoxy Silyl Ethers to β-Siloxy Aldehydes

DOI: 10.1021/ja00198a070

Source and publish data:

Journal of the American Chemical Society p. 6431 - 6432 (1989)

Update date:2022-08-11

Topics:

Authors:

Maruoka, Keiji

Ooi, Takashi

Yamamoto, Hisashi

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

Article abstract of DOI:10.1021/ja00198a070

Full text of DOI:10.1021/ja00198a070

Products guided by the article

Product name:2-METHYLUNDECANAL

Cas No:110-41-8

R&D Labs maybe for 110-41-8

suzhou chukai pharmateach co,.ltd

Contact:86-512-88812511

Address:Building 3, Wujiang Scientific Innovation Park, 2358 Changan Rd, Wujiang 215200, Jiangsu Province, P. R. China
Ningxia Soochow Agrochemical Limited Company

Contact:(+86）0512 6320 8190

Address:wujiang
Antimex Chemical Limied

website:http://www.antimex.com

Contact:0086-21-50563169

Address:Room1027,No.Jinyu Road,Pudong
Shandong Topscience Biotech Co., Ltd.

Contact:0633-2619278

Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China
Jiaozuo Zhongwei Special Products Pharmaceutical Co.,Ltd.

website:http://www.zw-pvp.com

Contact:15302105619

Address:Jiaozuo,Henan,China (Mainland)

Relevant to this article

Efficient consecutive four-component synthesis of 5-acylpyrid-2-ones initiated by copper-free alkynylation

Doi:10.1002/ejoc.201300235
(2013)
Synthesis of a novel prebiotic trisaccharide by a type i α-glucosidase from B. licheniformis strain TH4-2

Doi:10.1016/j.procbio.2010.09.018
(2011)
Reactions of tetrafluorohydrazine with diand triphenylphosphine. A new method for preparation of fluorophosphoranes

Doi:10.1021/ic50027a042
(1965)
Development of large-scale preparations of indole derivatives: Evaluation of potential thermal hazards and studies of reaction kinetics and mechanisms

Doi:10.1021/op060150f
(2006)
Preparation of pure meso-tetraphenylporphine and two derivatives.

Doi:10.1002/jps.2600610246
(1972)
Investigation of α-Thioglycoside Donors: Reactivity Studies toward Configuration-Controlled Orthogonal Activation in One-Pot Systems

Doi:10.1021/acs.orglett.6b01572
(2016)

Article Doi