000 -LEADER |
fixed length control field |
02140 a2200361 4500 |
003 - CONTROL NUMBER IDENTIFIER |
control field |
OSt |
005 - DATE AND TIME OF LATEST TRANSACTION |
control field |
20230306125112.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
fixed length control field |
230303b xxu||||| |||| 00| 0 eng d |
020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
ISBN |
9783031104565 |
040 ## - CATALOGING SOURCE |
Transcribing agency |
IIT Kanpur |
041 ## - LANGUAGE CODE |
Language code of text/sound track or separate title |
eng |
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER |
Classification number |
547 |
Item number |
P943 v.119 |
245 ## - TITLE STATEMENT |
Title |
Progress in the chemistry of organic natural products [Vol. 119] |
Remainder of title |
ancistrocladus naphthylisoquinoline alkaloids |
Statement of responsibility, etc |
edited by A. Douglas Kinghorn ... [et al.]; Doris Feineis and Gerhard Bringmann |
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) |
Name of publisher |
Springer |
Year of publication |
2023 |
Place of publication |
Switzerland |
300 ## - PHYSICAL DESCRIPTION |
Number of Pages |
xi, 335p |
440 ## - SERIES STATEMENT/ADDED ENTRY--TITLE |
Title |
Progress in the chemistry of organic natural products |
490 ## - SERIES STATEMENT |
Series statement |
/ edited by A. Douglas Kinghorn... [et al.] |
Volume number/sequential designation |
v.119 |
520 ## - SUMMARY, ETC. |
Summary, etc |
This book describes a unique class of secondary metabolites, the mono- and dimeric-naphthylisoquinoline alkaloids. They exclusively occur in lianas of the palaeotropical Ancistrocladaceae and Dioncophyllaceae plant families. Their unprecedented structures include stereogenic centers and rotationally hindered, and therefore stereogenic, axes. Extended recent investigations on six Ancistrocladus species from Asia, as reported in this contribution, shed light on their fascinating phytochemical productivity, with over 100 intriguing natural products. This high chemodiversity arises from a similarly unique biosynthesis from acetate-malonate units, following a novel polyketidic pathway to plant-derived isoquinoline alkaloids. Some of the compounds show most promising anti-parasitic activities. Additionally, strategies for the regio- and stereoselective total synthesis of the alkaloids, including the directed construction of the chiral axis, are also presented. |
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical Term |
Natural products |
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical Term |
Chemistry, Organic |
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical Term |
Ancistrocladus |
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical Term |
Naphthylisoquinoline |
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical Term |
Alkaloids |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Kinghorn, A. Douglas [ed.] |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Falk, Heinz [ed.] |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Gibbons, Simon [ed.] |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Asakawa, Yoshinori [ed.] |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Liu, Ji-Kai [ed.] |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Dirsch, Verena M. [ed.] |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Feineis, Doris |
700 ## - ADDED ENTRY--PERSONAL NAME |
Personal name |
Bringmann,Gerhard |
942 ## - ADDED ENTRY ELEMENTS (KOHA) |
Koha item type |
Books |