MONOTERPENOIDS-V. (+)-CARVONE FROM (+)-CAR-3-ENE

DOI: 10.1016/S0040-4020(01)96660-8

Source and publish data:

Tetrahedron p. 3083 - 3090 (1985)

Update date:2022-08-05

Topics:

Authors:

Shastri, M. H.

Patil, D. G.

Dev, Sukh

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

Article abstract of DOI:10.1016/S0040-4020(01)96660-8

A stereoselective conversion of the readily available (+)-car-3-ene into (+)-carvone by two different routes is described.This is the first report on synthesis of carvone from car-3-ene.

Full text of DOI:10.1016/S0040-4020(01)96660-8

Products guided by the article

Product name:(+)-trans-p-mentha-5,8-dien-2-ol

Cas No:4700-99-6

R&D Labs maybe for 4700-99-6

Maithili Life Sciences

Contact:+91 9963263336

Address:Plot#146A, IDA Mallapur, Hyderabad - 500072
Xi'an Galaxy Chemicals CO., Ltd

Contact:86-29-89380370

Address:No.8, Gaoxin three road, Xi'an city.
Zouping Fuhai Technology Development Co., Ltd.

Contact:+0532-86934525 18660293207

Address:jiuhu town industrial park Zouping County,bingzhou Provincejiuhu town industrial park
WUHU HUAHAI BIOLOGY ENGINEERING CO LTD

Contact:+86-553-3836920

Address:7/F NO.82 LAODONG ROAD WUHU CHINA
Shanghai Forever Biotech Co., Ltd.

Contact:+86-21-69734790

Address:Room 5017/5019、5022、5024 of Technology Innovation Centre, No.1155, Gongyuan East Rd, QingPu District, Shanghai China.

Relevant to this article

A convenient cyanide-free one-pot synthesis of nido-Me₃N-7-CB₁₀H₁₂ and nido-7-CB₁₀H₁₃^-

Doi:10.1039/b200930g
(2002)
Stereoselective synthesis of (+)-11βH,13-dihydroestafiatin, (+)-11βH,13-dihydroludartin, (-)-compressanolide, and (-)-11βH,13-dihydromicheliolide from santonin

Doi:10.1021/np020109f
(2002)
Regioselective glycosylation of unprotected phenyl 1-thioglycopyranosides with phenylboronic acid as a transient masking group

Doi:10.1002/ejoc.201300723
(2013)
Synthesis of both enantiomers of flavanone and 2-methylchromanone

Doi:10.1002/1522-2675(200210)85:10<3473::AID-HLCA3473>3.0.CO;2-7
(2002)
Jasisoquinolines A and B, architecturally new isoquinolines, from a marine sponge Jaspis sp.

Doi:10.1021/ol201823w
(2011)
Doi:10.1021/ja01634a025
(1954)

Article Doi