23 related articles for article (PubMed ID: 15858648)
1. Syntheses of Tetrahydropyran Type 8,7'-Neolignans Using a Ring-Expansion Reaction and Tetrahydrofuran Type 8,7'-Neolignans to Discover a Novel Phytotoxic Neolignan.
Tanaka M; Nishiwaki H; Yamauchi S
J Agric Food Chem; 2023 Jun; 71(23):9148-9156. PubMed ID: 37253419
[TBL] [Abstract][Full Text] [Related]
2. Stereoselective syntheses of all stereoisomers of lariciresinol and their plant growth inhibitory activities.
Nishiwaki H; Kumamoto M; Shuto Y; Yamauchi S
J Agric Food Chem; 2011 Dec; 59(24):13089-95. PubMed ID: 22066904
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of all stereoisomers of 3,3'-dimethoxy-7,7'-epoxylignane-4,4'-diol and their plant growth inhibitory activity.
Nishiwaki H; Nakayama K; Shuto Y; Yamauchi S
J Agric Food Chem; 2014 Jan; 62(3):651-9. PubMed ID: 24417732
[TBL] [Abstract][Full Text] [Related]
4. Use of the benzyl mesylate for the synthesis of tetrahydrofuran lignan: syntheses of 7,8-trans, 7',8'-trans, 7,7'-cis, and 8,8'-cis-virgatusin stereoisomers.
Yamauchi S; Nakato T; Tsuchiya M; Akiyama K; Maruyama M; Sugahara T; Kishida T
Biosci Biotechnol Biochem; 2007 Sep; 71(9):2248-55. PubMed ID: 17827688
[TBL] [Abstract][Full Text] [Related]
5. Antifungal activity of tetra-substituted tetrahydrofuran lignan, (-)-virgatusin, and its structure-activity relationship.
Akiyama K; Yamauchi S; Nakato T; Maruyama M; Sugahara T; Kishida T
Biosci Biotechnol Biochem; 2007 Apr; 71(4):1028-35. PubMed ID: 17420596
[TBL] [Abstract][Full Text] [Related]
6. Stereoselective construction of tetra-substituted tetrahydrofuran compounds from benzylic hemiacetal in the presence of H2 and a Pd catalyst: stereoselective synthesis of a stereoisomer of (-)-virgatusin and its antimicrobiological activity.
Nakato T; Tago R; Akiyama K; Maruyama M; Sugahara T; Kishida T; Yamauchi S
Biosci Biotechnol Biochem; 2008 Jan; 72(1):197-203. PubMed ID: 18175922
[TBL] [Abstract][Full Text] [Related]
7. Enantioselective synthesis of the tetrahydrofuran lignans (-)- and (+)-magnolone.
Nakato T; Yamauchi S
J Nat Prod; 2007 Oct; 70(10):1588-92. PubMed ID: 17887723
[TBL] [Abstract][Full Text] [Related]
8. First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol.
Yamauchi S; Kinoshita Y
Biosci Biotechnol Biochem; 2001 Jul; 65(7):1559-67. PubMed ID: 11515539
[TBL] [Abstract][Full Text] [Related]
9. First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan.
Yamauchi S; Okazaki M; Akiyama K; Sugahara T; Kishida T; Kashiwagi T
Org Biomol Chem; 2005 May; 3(9):1670-5. PubMed ID: 15858648
[TBL] [Abstract][Full Text] [Related]
10. Synthetic studies on optically active furofuran and diarylbutane lignans.
Mori N
Biosci Biotechnol Biochem; 2018 Jan; 82(1):1-8. PubMed ID: 29207906
[TBL] [Abstract][Full Text] [Related]
11. Synthesis of 3,4-dibenzyltetrahydrofuran lignans (9,9'-epoxylignanes).
Pohjoispää M; Wähälä K
Molecules; 2013 Oct; 18(11):13124-38. PubMed ID: 24284480
[TBL] [Abstract][Full Text] [Related]
12. Mr. Evans's Pathological and Practical Remarks on Ulcerations of the Genital Organs.
Med Chir Rev J Med Sci Anal Ser; 1820 Jun; 1(1):28-40. PubMed ID: 29917376
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
