An Efficient Enantioselective Synthesis of (-)-Serricorole

DOI: 10.1002/hlca.19930760314

Source and publish data:

Helvetica Chimica Acta p. 1275 - 1281 (1993)

Update date:2022-08-03

Topics:

Authors:

Oppolzer, Wolfgang

Rodriguez, Ines

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

Article abstract of DOI:10.1002/hlca.19930760314

The cigarette beetle pheromone (-)-serricorole (1) has been synthesized in 23percent overall yield by an eight-step sequence starting from N-propionylsultam 3.The synthesis features asymmetric anti- and syn-aldolizations 3 -> 4 and 8 -> 9, a non-destructi

Full text of DOI:10.1002/hlca.19930760314

Products guided by the article

Product name:(2S,3R)-2-ethyl-6-[(2S)-3-hydroxypentan-2-yl]-3,5-dimethyl-2,3-dihydro-4H-pyran-4-one

Cas No:86797-90-2

R&D Labs maybe for 86797-90-2

Zhuhai Rundu Pharmaceutical co.,Ltd

Contact:+86-756-7630755

Address:No.6,North Airport Road,Sanzao Town,Jinwan District
Wuhan Sunrise Pharmaceutical Technology Co., Ltd

Contact:+86-27-83314682

Address:Room 340, New material Industrial base No.17, Gu Tian Five Lu , Qiaokou District, Wuhan , China
Esuccess Material Limited

Contact:852-29282288

Address:HONGKONG
Shangyu Sanhechemicals Co.,LTD.

Contact:86-0571-56696839

Address:Num.2952,Nanhuan Road,Binjiang District,Hangzhou,China
Hebei Fulong Import & Export Co., Ltd.

Contact:86-311-87795661

Address:15A19 Zhongyuan Building,368 Youyi North Street,Shijiazhuang 050070,China

Relevant to this article

A highly enantioselective chemoenzymatic synthesis of syn-3-amino-2-hydroxy esters: Key intermediates for taxol side chain and phenylnorstatine

Doi:10.1016/j.tetasy.2005.08.015
(2005)
Doi:10.1016/S0277-5387(00)81520-X
(1983)
An outside-in approach to adjacent bistetrahydrofuran annonaceous acetogenins with C₂ core symmetry. Total synthesis of asimicin and a C32 analogue

Doi:10.1021/ol061352z
(2006)
1,5-Disubstituted 1,2,3-Triazole-Containing Peptidotriazolamers: Design Principles for a Class of Versatile Peptidomimetics

Doi:10.1002/chem.201704583
(2018)
Transformation of D-Xylose to (1R,2R,3R,4R)-2,3,4-Trihydroxy-1-(hydroxymethyl)cyclopentane, Pseudo-β-D-arabinofuranose

Doi:10.1246/bcsj.60.3673
(1987)
The reaction of 2,3:6,7-di-O-isopropylidene-5-O-methanesulphonyl-L-glycero-D-manno-heptofuranose with sodium methoxide: an aldehyde-group participation

Doi:10.1016/0008-6215(87)80254-9
(1987)

Article Doi