Diastereoselectivity Control in Photosensitized Addition of Methanol to (R)-(+)-Limonene-Reference-Cited by-同舟云学术

Diastereoselectivity Control in Photosensitized Addition of Methanol to (R)-(+)-Limonene

Published:2002-07-13 Issue:16 Volume:67 Page:5718-5726
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shim Sang Chul¹,Kim Dong Suk¹,Yoo Dong Jin¹,Wada Takehiko¹,Inoue Yoshihisa¹

Affiliation:

1. Center for Molecular Design and Synthesis, Department of Chemistry and School of Molecular Science (BK-21), Korea Advanced Institute of Science and Technology (KAIST), 373-1 Guseong-Dong, Yuseong-Gu, Daejeon 305-701, Korea, Department of Chemistry, Seonam University, Namwon 590-711, Korea, ICORP Entropy Control Project, JST, 4-6-3 Kamishinden, Toyonaka 560-0085, Japan, and Department of Molecular Chemistry, Osaka University, 2-1 Yamada-oka, Suita 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo025782o

Reference58 articles.

1. Asymmetric Induction during Energy Transfer1

2. Asymmetric Induction during Energy Transfer1

3. Asymmetric photochemistry in solution

4. Highly efficient photochemical addition of tertiary amines to electron deficient alkenes. Diastereoselective addition to (5R)-5-menthyloxy-2[5H]-furanone

5. Stereoselective radical addition of tertiary amines to (5R)-5-menthyloxy-2[5H]-furanone: Application to the enantioselective synthesis of (−)-isoretronecanol and (+)-laburnine

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