Asymmetric Diels-Alder reaction catalyzed by a chiral ytterbium trifluoromethanesulfonate

DOI: 10.1016/0040-4039(93)88078-W

Source and publish data:

Tetrahedron Letters p. 4535 - 4538 (1993)

Update date:2022-08-30

Topics:

Authors:

Kobayashi

Hachiya Hachiya

Ishitani

Araki Araki

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

Article abstract of DOI:10.1016/0040-4039(93)88078-W

In the presence of a catalytic amount of chiral ytterbium trifluoromethanesulfonate (triflate), acyl-1,3-oxazolidin-2-ones or methacrolein reacted with cyclopentadiene to afford the corresponding Diels-Alder adduct in high yields and with moderate to exce

Full text of DOI:10.1016/0040-4039(93)88078-W

Products guided by the article

Product name:2-Oxazolidinone, 3-[[(1S,2R,3R,4R)-3-phenylbicyclo[2.2.1]hept-5-en-2-yl]carbonyl]-

Cas No:109299-98-1

R&D Labs maybe for 109299-98-1

Chongqing maohuan Chemicals Co., Ltd

website:http://www.bschem.com

Contact:+86 13996103726

Address:Chongqing Nan'an District Tu Town
Shanghai PotentPharm Science and Technology Co.,Ltd

Contact:86-021-51969655

Address:Unit B, Building 18, No.300, Chuantu Rd,Pudong District, Shanghai 201202, China
Jiangsu Allyrise Pharmaceutical Co., Ltd.(expird)

Contact:+86-523-86818997

Address:Taizhou,Jiangsu Province,CHINA
Esuccess Material Limited

Contact:852-29282288

Address:HONGKONG
wuxi huabin bio-tech Co.,Ltd(expird)

Contact:86-0510-85133006

Address:hubin road NO157

Relevant to this article

Doi:10.1021/ja01678a039
(1925)
Pyridazine derivatives. Part 40: Reactivity of 5-alkynylpyridazin-3(2H)- ones toward hydrochloric acid

Doi:10.1016/j.tet.2005.03.021
(2005)
Enantioselective aza-Henry reaction using cinchona organocatalysts

Doi:10.1016/j.tet.2005.09.076
(2006)
Fluorite-like phases in the BaF₂-BiF₃-Bi ₂O₃ system - Synthesis, conductivity and defect clustering

Doi:10.1016/j.materresbull.2005.02.007
(2005)
Characterization of an acid hydrolysis product of starfish toxins as a 5 -pregnane derivative.

Doi:10.1021/ja00766a087
(1972)
Study on the cleavage of alkyl-: O -aryl bonds by in situ generated hydroxyl radicals on an ORR cathode

Doi:10.1039/c7ra11236j
(2017)

Article Doi