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

Jurong Huaheng Natural Biological Products Factory

website:http://www.risebiochem.com

Contact:+86-13921007726

Address:Chuncheng town,Jurong city,Jiangsu province,China
wuxi leji biology technology co., LTD

website:http://www.lejibio.com/

Contact:18362718864

Address:The Nanyue Road No. 2, Yixing City, Jiangsu Province
Beijing Century Richap Chemistry Co.,Ltd

Contact:+86- 010-64455497

Address:Guannan County, Lianyungang City, Jiangsu Province, China
Shao Xing Empire Import&Export CO.,ltd

Contact:86-575-82127757

Address:11#, Weiwu Road, Shangyu Industrial Park, Hangzhou Bay, Hangzhou, Zhejiang Province, China
Jiangxi Biochem Co.,Ltd

Contact:86-791-86629460

Address:1-6F, 118 Xinzhou road, Nanchang, Jiangxi, China

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