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- 01HG0RNMHG2R2XQPCZF1XT8906 classification C3.
- 01HG0RNMHG2R2XQPCZF1XT8906 date "1980".
- 01HG0RNMHG2R2XQPCZF1XT8906 language "eng".
- 01HG0RNMHG2R2XQPCZF1XT8906 type conference.
- 01HG0RNMHG2R2XQPCZF1XT8906 hasPart 01HG0RYWE40YC7JB41A0HWADCF.pdf.
- 01HG0RNMHG2R2XQPCZF1XT8906 subject "Chemistry".
- 01HG0RNMHG2R2XQPCZF1XT8906 presentedAt urn:uuid:486f98e2-cc1b-4fb5-8083-583091011a63.
- 01HG0RNMHG2R2XQPCZF1XT8906 abstract "Many sesquiterpenes contain angularly substituted hydrindane or decalane skeletons. These are easily accessible via a (_2 + _2)photoreaction between appropriately substituted 2-cyclopentenones or 2-cyclohexenones and 1,2-bis(trimethylsiloxy)cyclobutene, followed by hydroclytic cleavage of the four-membered ring. Further chemical transformations afford selected sequiterpenes, as is illustrated by the total synthesis of (-)dihydrodictyopterone starting from (-)piperitone.".
- 01HG0RNMHG2R2XQPCZF1XT8906 author 6F40B448-B25E-11E6-B104-2D2FD0AF0289.
- 01HG0RNMHG2R2XQPCZF1XT8906 author F373969A-F0ED-11E1-A9DE-61C894A0A6B4.
- 01HG0RNMHG2R2XQPCZF1XT8906 author urn:uuid:6b62b337-bba8-4248-bf13-544d9d4e963d.
- 01HG0RNMHG2R2XQPCZF1XT8906 dateCreated "2023-11-24T13:35:24Z".
- 01HG0RNMHG2R2XQPCZF1XT8906 dateModified "2024-11-28T00:09:18Z".
- 01HG0RNMHG2R2XQPCZF1XT8906 name "The total synthesis of (-)dihydrodictyopterone : a photochemical synthetic approach to sesquiterpenes".
- 01HG0RNMHG2R2XQPCZF1XT8906 pagination urn:uuid:07929fd6-ea4a-4214-910f-86a7ae849461.
- 01HG0RNMHG2R2XQPCZF1XT8906 sameAs LU-01HG0RNMHG2R2XQPCZF1XT8906.
- 01HG0RNMHG2R2XQPCZF1XT8906 sourceOrganization urn:uuid:246cb510-ef49-4414-a039-860931505594.
- 01HG0RNMHG2R2XQPCZF1XT8906 type C3.