Synthetic studies of alpha-tocopherol. I. Synthesis of alpha-Tocopheryl acetate.

DOI: 10.1246/bcsj.41.1224

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1224 - 1228 (1968)

Update date:2022-08-04

Topics:

Authors:

Ichikawa

Kato Kato

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

Article abstract of DOI:10.1246/bcsj.41.1224

Full text of DOI:10.1246/bcsj.41.1224

Products guided by the article

Product name:(2S,4'R,8'R)-α-Tocopherylacetat

Cas No:79200-47-8

R&D Labs maybe for 79200-47-8

SAGECHEM LIMITED

website:http://www.sagechem.com

Contact:+86-571-86818502

Address:Room C1301, New Youth Plaza, 8 Jia Shan Road, Hangzhou, China
Shandong Shouguang Songchuan Industrial Additives Co.,Ltd

Contact:+86-536-8566856

Address:Shouguang,Shandong,China
wuxi huabin bio-tech Co.,Ltd(expird)

Contact:86-0510-85133006

Address:hubin road NO157
Neworld Chemical Co., Ltd Shanghai(expird)

Contact:+86-21-62202658

Address:11F, Blvd 2, No. 1969 PuXing Rd, Shanghai
Tianjin Hedong Red Cliff Chemical Reagent Factory

Contact:+86-022-84780548

Address:Li Ming Zhuang Gong Ye Yuan,Dongli District,Tianjin,China

Relevant to this article

PRACTICAL METHOD FOR USING ALKOXIDE-ACCELERATED VINYLCYCLOBUTANE RING EXPANSIONS IN THE SYNTHESIS OF SIX-MEMBERED RINGS. UNEXPECTED ORBITAL SYMMETRY ALLOWED AND FORBIDDEN 1,3-SIGMATROPIC REARRANGEMENTS.

Doi:10.1021/ja00341a035
(1983)
Synthesis of 1,3,5-Trialkylbenzenes from Anils of Methyl Alkyl Ketones

Doi:10.1021/jo00335a046
(1981)
Asymmetric Hydroformylation of Heterocyclic Olefins Mediated by Supramolecularly Regulated Rhodium-Bisphosphite Complexes

Doi:10.1021/acs.joc.5b01805
(2015)
Dipole-Stabilized Carbanions: Secondary (α-Lithioalkyl)alkylamine Synthetic Equivalents from N,N-dialkyl-2,2-diethylbutyramides

Doi:10.1021/jo00334a052
(1981)
Design and synthesis of novel small molecule N/OFQ receptor antagonists

Doi:10.1016/j.bmcl.2003.11.083
(2004)
Synthesis of 5-alkyl-5-aryl-γ-lactams from 1-aryl-substituted nitroalkanes and methyl acrylate via Michael addition and reductive lactamization

Doi:10.1016/j.tet.2014.04.074
(2014)

Article Doi