Synthesis of Phenylselenopyrans and Lactones from Allylic Alcohols and Acids via Baylis-Hillman Reaction-Reference-Cited by-同舟云学术

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Synthesis of Phenylselenopyrans and Lactones from Allylic Alcohols and Acids via Baylis-Hillman Reaction

Published:2017-09-21 Issue:27 Volume:2 Page:8402-8407
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Reddy Thatikonda Narendar¹²^ORCID,Swetha Chanda¹,Ramesh Perla³,Sridhar Balasubramanian⁴,Jayathirtha Rao Vaidya¹⁵

Affiliation:

1. Crop Protection Chemicals Division; CSIR-Indian Institute of Chemical Technology; Uppal Road, Tarnaka Hyderabad 500007 India

2. Genomics Research Center; Academia Sinica; 128 Academia Road, Section 2, Nankang Taipei 115 Taiwan (ROC).

3. CSIR-Indian Institute of Chemical Technology; Uppal Road, Tarnaka Hyderabad 500007 India

4. Centre for X-ray Crystallography; CSIR-Indian Institute of Chemical Technology; Uppal Road, Tarnaka Hyderabad 500007 India

5. AcSIR, CSIR-Indian Institute of Chemical Technology; Uppal Road, Tarnaka Hyderabad 500007 India

Funder

CSIR-New Delhi

CSIR-UGC New Delhi

Publisher

Wiley

Subject

General Chemistry

Reference144 articles.

1. A new route to substituted 3-methoxycarbonyldihydropyrans; enantioselective synthesis of (–)-methyl elenolate

2. Synthesis and biological evaluation of a spongistatin AB-spiroketal analogue

3. Antineoplastic agents. 257. Isolation and structure of spongistatin 1

4. Iron-catalyzed cross-coupling between C-bromo mannopyranoside derivatives and a vinyl Grignard reagent: toward the synthesis of the C31–C52 fragment of amphidinol 3

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1. Importance of Baylis-Hillman adducts in modern drug discovery;Tetrahedron Letters;2018-07

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