Enzymatic Preparation of Enantiomerically Enriched Tertiary α-Benzyloxy Acid Esters. Application to the Synthesis of (S)-(-)-Frontalin

DOI: 10.1021/jo00302a031

Source and publish data:

Journal of Organic Chemistry p. 4643 - 4647 (1990)

Update date:2022-08-04

Topics:

Authors:

Sugai, Takeshi

Kakeya, Hideaki

Ohta, Hiromichi

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

Article abstract of DOI:10.1021/jo00302a031

Enzymatic preparation of enantiomerically enriched tertiary α-benzyloxy acid esters is described.Enantioselective hydrolysis of the racemic esters of the formula by lipase OF (from Candida cylindracea, Meito Sangyo Co.) was succes

Full text of DOI:10.1021/jo00302a031

Products guided by the article

Product name:2-Benzyloxy-2-methyl-undecanoic acid methyl ester

Cas No:128549-15-5

R&D Labs maybe for 128549-15-5

LINYI FUDE FINE CHEMICAL CO.,LTD

Contact:86-539-2361184

Address:YISHUI, LINYI,SAHNDONG,CHINA
henan victory industry co.ltd

Contact:86-371-63655023

Address:No.85,jinshui road,zhengzhou,China
Anhui Asahikasei Chemical Co., Ltd

Contact:86-551-4259770

Address:No. 88 Linquan Road Hefei Anhui China
Guangzhou Chemical Reagent Factory

Contact:+86-20-8435 9820 or 8435 7345

Address:Southern Guangzhou, Guangdong, China
hangzhou verychem science and technology co.ltd

website:http://www.verypharm.com

Contact:+86-571-88162785; 88162786

Address:F1502, 753 Shenhua road, Hangzhou, China

Relevant to this article

Synthesis of three-, four-, and five-membered dimethalloheterocyclic compounds by reaction of the hydride 2> (R = Me or Prⁱ) with unsaturated systems of the type X<*>Y and X'=Y'=Z'. Crystal structures of repr

Doi:10.1016/0022-328X(90)80263-Y
(1990)
Synthesis of a neolactotetraose glycoside suitable for enzymatic elaboration to the sialyl lewis X stage

Doi:10.1080/07328309808002327
(1998)
Deprotonation of β-diketiminate in sterically demanding β-(diketiminato)-lanthanide complexes: Influence of lanthanide metals

Doi:10.1002/ejic.201000759
(2011)
Relative Rates for the Addition Reactions of the Malonyl Radical to Substituted Styrenes Induced by Cerium(IV) Ammonium Nitrate and Tributyltin Hydride. A Comparison

Doi:10.1021/jo00309a010
(1990)
An expeditious asymmetric synthesis of the pentacyclic core of the cortistatins by an intramolecular (4+3) cycloaddition

Doi:10.1039/c1cc00087j
(2011)
BIOSYNTHESIS OF INDOLE ALKALOID TUMOR PROMOTERS TELEOCIDINS (I) POSSIBLE BIOSYNTHETIC PATHWAY OF THE MONOTERPENOID MOIETIES OF TELEOCIDINS

Doi:10.1016/S0040-4020(01)88371-X
(1990)

Article Doi