INTRAMOLECULAR CYCLOADDITION REACTIONS OF EXOCYCLIC NITRONES APPLICATION IN THE TOTAL SYNTHESIS OF TERPENES

DOI: 10.1016/S0040-4020(01)96702-X

Source and publish data:

Tetrahedron p. 3479 - 3495 (1985)

Update date:2022-08-04

Topics:

Authors:

Funk, Raymond L.

Bolton, Gary L.

Daggett, Joy Umstead

Hansen, Marvin M.

Horcher, Linus H. M.

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

Article abstract of DOI:10.1016/S0040-4020(01)96702-X

Exocyclic nitrones smoothly participate in intramolecular cycloaddition reactions to provide bridged and fused polycarbocycles.The exploitation of this methodology in the total syntheses of the sesquiterpenes (+/-)-7,12-secoishwaran-12-ol (44), (+/-)-hirs

Full text of DOI:10.1016/S0040-4020(01)96702-X

Products guided by the article

Product name:(1S,5R,7R)-8-Allyl-2-benzyl-3-oxa-2-aza-tricyclo[5.3.1.0^1,5]undecane

Cas No:86437-32-3

R&D Labs maybe for 86437-32-3

ALPHA PHARMACEUTICAL CO，LTD JIANGSU

Contact:+86-527-84829968,+86-527-84829998

Address:suqian city
ClickChem Technology Co., Limited

Contact:+86-0310-6519966/0531-52893837

Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Beijing Greenchem Technology Co.,Ltd. ( Panjin Greenchem Technology Co.Ltd .)

website:http://www.bjgreenchem.com/

Contact:+86-427-6515887

Address:301,302, 3rd Floor, Building C-7, Dongsheng Science Park, Northern Territory, Zhongguancun, No. 66, Xixiaokou Road, Haidian District, Beijing
SHANGHAI ARCADIA BIOTECHNOLOGY LTD.

Contact:+86-21-61353236

Address:SUITE 901, BUILDING WENSLI, 1378 LU JIA BANG RD, SHANGAHI 200011, P.R.CHINA
Improve Medical Technology(Nanxiong) Co., Ltd

Contact:86-751-3836997

Address:No.33, Pingan First Road, Fine Chemical Industry Base, Nanxiong City, Shaoguan, Guangdong, China

Relevant to this article

Structurally diverse second-generation [2.2]paracyclophane ketimines with planar and central chirality: Syntheses, structural determination, and evaluation for asymmetric catalysis

Doi:10.1002/chem.200500146
(2005)
Visible-light-promoted oxidative difunctionalization of alkenes with sulfonyl chlorides to access β-keto sulfones under aerobic conditions

Doi:10.1016/j.tetlet.2017.08.013
(2017)
ALKYLATION OF SILYL ETHERS OF ENOLS BY EPISULFONIUM SALTS AND β-HALOALKYL ARYL SULFIDES AS A METHOD FOR THE INTRODUCTION OF THE β-ARYLTHIOALKYL GROUP INTO CARBONYL COMPOUNDS

Doi:10.1007/BF00954288
(1983)
Synthetic approach to cytochalasins

Doi:10.1021/jo00339a027
(1981)
Synthesis of 2,4-diarylimidazoles through Suzuki cross-coupling reactions of imidazole halides with arylboronic acids

Doi:10.3987/COM-05-10445
(2005)
Facile regio- and diastereoselective syntheses of hydroxylated 2-aminocyclohexanecarboxylic acids

Doi:10.1002/ejoc.200500062
(2005)

Article Doi