Scholarly article on (+)-2-CARENE 4497-92-1 from Journal of the American Chemical Society p. 1925,1932

DOI: 10.1021/ja00984a030

Source and publish data:

Journal of the American Chemical Society p. 1925,1932 (1967)

Update date:2022-08-17

Topics:

Authors:

Acharya Acharya

Brown Brown

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

Article abstract of DOI:10.1021/ja00984a030

Full text of DOI:10.1021/ja00984a030

Products guided by the article

Product name:(+)-2-CARENE

Cas No:4497-92-1

R&D Labs maybe for 4497-92-1

Weifang Dongxing Chitosan Factory

website:http://dxchitosan.lookchem.com/

Contact:13475651157

Address:Weifang city ,shandong province
Tianjin Ingenochem Technology Co.,Ltd

Contact:+86-22-23677060

Address:Hitech Green Industry Park K2-9-602, Nankai district
Hisyntech Corporation Limited

Contact:0086-22-23410962

Address:17-201, Ningfuli, Shuishanggongyuandong road,Nankai district, Tianjin, China
Xi'an Costrong Pharmaceutical Co., Ltd.

Contact:029- 68576496

Address:Room 2004,Shuibao Building,No.190,South Erhuan Rd, Yanta District,Xi'an,Shaan Xi,China
Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China

Relevant to this article

Biomimetic Approaches Employing the Ugi Five-Center Four-Component Reaction for Synthesis of the Right-Hand Portion of Halichonadin Q and the Central Part of Halichonadin M

Doi:10.1055/s-0034-1380438
(2015)
Doi:10.1021/jo01031a047
(1964)
Doi:10.1039/P19790002675
(1979)
The reaction of transdecahydroquinoline with molecular oxygen.

Doi:10.1007/BF02318504
(1954)
Synthesis of 3-Benzo[b]thienyl 3-Thienyl Ether via an Addition-Elimination Reaction and Its Transformation to an Oxygen-Fused Dithiophene Skeleton: Synthesis and Properties of Benzodithienofuran and Its π-Extended Derivatives

Doi:10.1021/acs.orglett.7b00969
(2017)
2′-Deoxy-2′-azidonucleoside analogs: synthesis and evaluation of antitumor and antimicrobial activity

Doi:10.1007/s11696-017-0339-9
(2018)

Article Doi

DOI: 10.1021/ja00984a030