Di-l-menthyl (Acetoxymethylene)malonate, a New Chiral Dienophile: Enantioselective Route to Carbocyclic Analogues of C-Nucleoside

DOI: 10.1021/jo00236a057

Source and publish data:

Journal of Organic Chemistry p. 226 - 227 (1988)

Update date:2022-09-26

Topics:

Authors:

Katagiri, Nobuya

Haneda, Toru

Hayasaka, Etsuko

Watanabe, Nobuhisa

Kaneko, Chikara

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

Article abstract of DOI:10.1021/jo00236a057

Titanium tetrachloride promoted Diels-Alder reaction of new chiral dienophile, di-l-menthyl (acetoxymethylene)malonate, with cyclopentadiene not only proceeds with high diastereofacial selectivity but also provides an efficient enantioselective synthetic

Full text of DOI:10.1021/jo00236a057

Products guided by the article

Product name:2-Hydroxymethylene-malonic acid bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester

Cas No:111998-71-1

R&D Labs maybe for 111998-71-1

zhuzhou zhongle chemical co. ltd.

Contact:+86-0731 28228409

Address:Zhuzhou, Hunan, China
Shanghai united Scientific Co.,Ltd.

Contact:+86-21-53535353

Address:28F No.900 huaihai Road Shanghai China
Suzhou Health Chemicals Co., Ltd.

website:http://www.healthchems.com

Contact:13776257979

Address:No. 338, Jingang Avenue,
Shanghai Micro-mega Industry Co., Ltd.

Contact:0086-21-34628682;57153848

Address:Rm413,No.413,West Meilong Road, Minhang District,Shanghai P R China
Phytomarker Ltd.(expird)

Contact:+86-22-26358246

Address:601-4-20, Fujiayuan, Tiantai Road, Hebei District, Tianjin, China

Relevant to this article

Doi:10.1007/BF00899592
(1956)
PREPARATION OF A FRAGMENT OF THE CELL WALL TEICHOIC ACID OF BACILLUS LICHENIFORMIS ATCC 9945 VIA A SOLID PHASE APPROACH

Doi:10.1016/S0040-4039(01)81041-8
(1987)
Fluoro(nitrile)xenon(II) Cations, RC(*)N-XeF⁺AsF6^- (R = H, CH3, CH2F, C2H5, C2F5, C3F7, or C6F5); Novel Examples of Xenon-Nitrogen Bonds and 129Xe-13C, 129Xe-1H, and 129Xe-14N Nuclear Spin-Spin Couplings

Doi:10.1039/c39870001644
(1987)
Indolynes as electrophilic indole surrogates: Fundamental reactivity and synthetic applications

Doi:10.1021/ol802958a
(2009)
Stereoselective Syntheses of Hydroxyethylene Dipeptide Isosteres

Doi:10.1021/jo00001a083
(1991)
Cross-coupling of aryl/alkenyl pivalates with organozinc reagents through nickel-catalyzed C-O bond activation under mild reaction conditions

Doi:10.1002/anie.200803814
(2008)

Article Doi