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Strategies and tactics in organic synthesis : Vol. 10 / (Record no. 246933)

000 -LEADER
fixed length control field 04443cam a2200481Mi 4500
001 - CONTROL NUMBER
control field ocn913618259
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20190328114808.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
fixed length control field m o d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr cn|||||||||
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 140719s2014 vtu o 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency UAB
Language of cataloging eng
Description conventions pn
Transcribing agency UAB
Modifying agency OCLCO
-- EBLCP
-- OPELS
-- N$T
-- NOC
-- YDXCP
-- OCLCF
-- DEBSZ
-- UIU
-- OCLCQ
-- ESU
-- OCLCQ
-- U3W
-- D6H
-- YOU
-- DEBBG
066 ## - CHARACTER SETS PRESENT
Alternate G0 or G1 character set (S
019 ## -
-- 884014639
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9780124171916
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 0124171915
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 9780124171855
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)913618259
Canceled/invalid control number (OCoLC)884014639
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number QD262
072 #7 - SUBJECT CATEGORY CODE
Subject category code SCI
Subject category code subdivision 013040
Source bisacsh
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 547.2
245 00 - TITLE STATEMENT
Title Strategies and tactics in organic synthesis : Vol. 10 /
Medium [electronic resource]
Statement of responsibility, etc. edited by Michael Harmata.
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc. Burlington :
Name of publisher, distributor, etc. Elsevier Science,
Date of publication, distribution, etc. 2014.
300 ## - PHYSICAL DESCRIPTION
Extent 1 online resource.
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
490 1# - SERIES STATEMENT
Series statement Strategies and Tactics in Organic Synthesis ;
Volume/sequential designation v. 10
588 0# - SOURCE OF DESCRIPTION NOTE
Source of description note Print version record.
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note Substrate-Directed Heck-Matsuda Arylations; ( -- )-Berkelic Acid: Lessons Learned From Our Investigations on a Scalable Total Synthesis; The Mysterious Case of the Kingianins; Total Synthesis of Chinensiolide B: An Exercise in Functional Group Selectivity with the Help of a Fortuitous Side Product and a Good Nose; Syntheses of the Bisindole Alkaloids of the Genera Borreria and Flindersia; Synthesis of (�)-Amathaspiramide F: Stereochemical Switch of a [2,3]-Stevens ; Oxabicyclic Building Blocks as Key Intermediates in the Synthesis of the Natural Products ( -- )-Platensimycin and (+)-Frondosin A; Structure Inspires a New Method That Delivers the Synthesis of Natural Products and Analogs in the Pederin Family; Gliocladin C: The Development and Application of a Pyrroloindoline-Indole Radical Coupling Reaction; Studies in the Synthesis of Biaryl Natural Products: The 6,6'-Binaphthopyranones; Sleepless Nights: The Total Synthesis of the Anticancer Australian Rainforest Polyketide EBC-23; Total Synthesis of the Crinipellins.
520 ## - SUMMARY, ETC.
Summary, etc. A classic in the area of organic synthesis, Strategies and Tactics in Organic Synthesis provides a forum for investigators to discuss their approach to the science and art of organic synthesis. Rather than a simple presentation of data or a secondhand analysis, we are given stories that vividly demonstrate the power of the human endeavor known as organic synthesis and the creativity and tenacity of its practitioners.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Organic compounds
General subdivision Synthesis.
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element SCIENCE
General subdivision Chemistry
-- Organic.
Source of heading or term bisacsh
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Organic compounds
General subdivision Synthesis.
Source of heading or term fast
Authority record control number (OCoLC)fst01047668
655 #4 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Harmata, Michael.
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Print version:
Main entry heading Harmata, Michael.
Title Strategies and Tactics in Organic Synthesis.
Place, publisher, and date of publication Burlington : Elsevier Science, �2014
International Standard Book Number 9780124171855
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Strategies and Tactics in Organic Synthesis ;
Volume number/sequential designation v. 10.
856 40 - ELECTRONIC LOCATION AND ACCESS
Materials specified ScienceDirect
Uniform Resource Identifier http://www.sciencedirect.com/science/book/9780124171855
856 40 - ELECTRONIC LOCATION AND ACCESS
Materials specified ScienceDirect
Uniform Resource Identifier http://www.sciencedirect.com/science/bookseries/18746004/10
880 8# - ALTERNATE GRAPHIC REPRESENTATION
Linkage 505-00
a 7. Synthesis of Kingianin A8. ``Go Fish� � -Pursuit of the Intermolecular RCDA Approach; 9. Formal Synthesis of Kingianin A and Synthesis of Kingianins D, F, H, and J; 10. NCI 60 Test Results for Kingianins A (NSC#D-768505/1) and H (NSC#D-768506/1); 11. Reconsidering the Biosynthesis; 12. Conclusions; Acknowledgments; References; Chapter 4: Total Synthesis of Chinensiolide B: An Exercise in Functional Group Selectivity with the Help of a Fortuitous Side product and a good nose; 1. Introduction; 1.1. Chinensiolide and Other (Sa(B-Methylene (Sd(B-Lactones in Nature
880 8# - ALTERNATE GRAPHIC REPRESENTATION
Linkage 505-00
a 1.2. Traditional Methods for the Synthesis of (Sa(B-Methylene (Sd(B-Lactones1.3. Use of 2-Alkoxycarbonyl Allylboronates to Access (Sa(B-Methylene (Sd(B-Lactones; 2. Model Studies and Retrosynthetic Analysis; 2.1. Retrosynthetic Analysis; 2.2. Model Studies; 3. Design and Synthesis of the Key Allylboronate; 3.1. Selection of the Protecting Group; 3.2. Synthesis of Disubstituted Allylboronate 7; 4. Synthesis of the Cyclopentyl Aldehyde Substrate; 4.1. Literature Precedent; 4.2. Preparation of Aldehyde 6; 5. Critical Moment-The Key Aldehyde Allylboration Step

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